Active compound combinations

ABSTRACT

The present invention relates to active compound combinations, in particular within a fungicide composition, which comprise as compound (A) a compound of formula (I) and as compound (B) a further fungicidally active compound as specified below. Moreover, the invention relates to compositions comprising such compound combination and to the use of the compound combinations and the fungicide compositions as biologically active agent, especially for control of phytopathogenic fungi in crop protection and in the protection of industrial materials and as plant growth regulators.

The present invention relates to active compound combinations, in particular within a fungicide composition, which comprise as compound (A) a compound of formula (I) and as compound (B) a further fungicidally active compound as specified below. Moreover, the invention relates to compositions comprising such compound combination and to the use of the compound combinations and the fungicide compositions as biologically active agent, especially for control of phytopathogenic fungi in crop protection and in the protection of industrial materials and as plant growth regulators.

Throughout this application the terms “composition” and “formulation” are used synonymously and refer to mixtures of a compound combination of the invention and at least one agriculturally suitable auxiliary.

Albeit compounds of formula (I) provide excellent means in protecting plants from diseases caused by fungi, there is still need to even improve those means in order to address the ever increasing environmental and economic requirements imposed on modern-day crop protection agents and compositions. This includes, for example, improvement to the spectrum of action, safety profile, selectivity, application rate, formation of residues, and favourable preparation ability, and development of new compositions to deal with potential problems, like resistances.

The present invention provides active compound combinations and compositions comprising said combinations which at least in some aspects achieve the stated objective.

Accordingly, the present invention provides active compound combinations comprising

-   -   (A) at least one compound of formula (I)

wherein

-   -   A is selected from the group consisting of O, S, C(═O), S(═O),         S(═O)₂, NR¹ and CR¹R², with R¹ and R² being independently         selected from the group consisting of hydrogen C₁-C₆-alkyl and         C₃-C₈-cycloalkyl, or R¹ and R² form, together with the carbon         atom to which they are attached to, a C₃-C₈-cycloalkyl or a         non-aromatic 3- to 7-membered monocyclic heterocycle;     -   m is 0, 1 or 2;     -   T is selected from the group consisting of hydrogen, hydroxyl,         C₁-C₆-alkyl, —C(═O)R^(a1), —C(═O)(OR^(a1)), —C(═O)N(R^(a2))₂,         —S(═O)R^(a1), —S(═O)₂R^(a1) and S(═O)₂N(R^(a2))₂,     -   with R^(a1) being selected from the group consisting of         C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₃-C₈-cycloalkyl and         C₂-C₆-alkenyl,     -   with R^(a2) being independently selected from the group         consisting of hydrogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl,         C₃-C₈-cycloalkyl and C₂-C₆-alkenyl;     -   R³ and R⁴ are independently selected from the group consisting         of hydrogen, halogen, cyano, hydroxyl, formyl, carboxyl,         C₁-C₆-alkyl, C₁-C₆-alkoxy, C₁-C₆-alkylcarbonyl,         C₁-C₆-alkoxycarbonyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl,         C₃-C₈-cycloalkyl, aromatic C₆-C₁₄-carbocycle, aromatic 5- to         14-membered heterocycle, non-aromatic 3- to 14-membered         heterocycle and —O—Si(C₁-C₆-alkyl)₃, or R³ and R⁴ form, together         with the carbon atom to which they are attached to, a carbonyl,         a methylidene, a C₃-C₈-cycloalkyl or a non-aromatic 3- to         7-membered monocyclic heterocycle;     -   R⁵ is selected from the group consisting of hydrogen, hydroxyl,         C₁-C₆-alkyl, C₁-C₆-alkoxy, C₁-C₆-alkylcarbonyloxy,         C₁-C₆-alkylsulfanyl, C₁-C₆-alkylsulfinyl, C₁-C₆-alkylsulfonyl,         C₃-C₈-cycloalkyl and —O—Si(C₁-C₆-alkyl)₃;         wherein aliphatic R¹, R², R³, R⁴ and R⁵ substituents may be         substituted with one or more substituents independently selected         from the group consisting of halogen, cyano, amino, nitro,         hydroxyl, formyl, carboxyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy,         C₁-C₆-alkoxycarbonyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl,         —O—Si(C₁-C₆-alkyl)₃ and non-aromatic 3- to 7-membered monocyclic         heterocycle;         wherein cyclic R¹, R², R³, R⁴ and R⁵ substituents may be         substituted with one or more substituents independently selected         from the group consisting of halogen, cyano, nitro, hydroxyl,         formyl, oxo, methylidene, C₁-C₆-alkyl, C₁-C₆-haloalkyl,         C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₂-C₆-alkenyl, C₃-C₈-cycloalkyl,         C₃-C₈-halocycloalkyl, —O—Si(C₁-C₆-alkyl)₃ and non-aromatic 3- to         7-membered monocyclic heterocycle;     -   R³ or R⁴, and R⁵ may form, together with the carbon atom to         which they are attached to, a C₃-C₈-cycloalkyl;     -   L represents a direct bond or L is selected from the group         consisting of carbonyl, C₁-C₆-alkylene, C₁-C₆-alkylene         substituted on a same carbon atom by two substituents forming         together with the carbon atom to which they are attached to a         C₃-C₈-cycloalkyl, C₁-C₆-alkylene substituted on a same carbon         atom by two substituents forming together with the carbon atom         to which they are attached to a non-aromatic 3- to 7-membered         monocyclic heterocycle, C₂-C₆-alkenylene, C₂-C₆-alkynylene,         C₃-C₈-cycloalkylene, C₁-C₆-alkylene-C₃-C₈-cycloalkylene,         C₃-C₈-cycloalkylene-C₁-C₆-alkylene,         C₁-C₆-alkylene-C₃-C₈-cycloalkylene-C₁-C₆-alkylene,         C₁-C₆-alkylene-(C═O), C(═O)—C₁-C₆-alkylene,         C₃-C₈-cycloalkenylene, C₁-C₆-alkylene-C₃-C₈-cycloalkenylene,         C₃-C₈-cycloalkenylene-C₁-C₆-alkylene,         C₁-C₆-alkylene-C₃-C₈-cycloalkenylene-C₁-C₆-alkylene,         non-aromatic 3- to 7-membered monocyclic heterocyclylene,         —NR^(aL1)—, —NR^(aL1)(C═O), —C(═O)NR^(aL1)—, —NR^(aL1)S(═O)₂—,         —S(═O)₂NR^(aL1)—, —C(═NOR^(aL2))—, —C(═N—N(R^(aL2))₂) and         —C(═NR^(aL2))     -   with R^(aL1) being selected from the group consisting of         hydrogen and C₁-C₆-alkyl,     -   with R^(aL2) being independently selected from the group         consisting of hydrogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl,         C₃-C₈-cycloalkyl and C₂-C₆-alkylenyl,         wherein aliphatic L substituents may be substituted with one or         more L^(Sa) substituents that may be the same or different         wherein cyclic or cyclic moiety of L substituents may be         substituted with one or more L^(Sc) substituents that may be the         same or different,     -   L^(sa) is selected from the group consisting of halogen, cyano,         hydroxyl, carboxyl, methylidene, halomethylidene, C₁-C₆-alkoxy,         C₁-C₆-haloalkoxy, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl,         C₁-C₆-alkoxycarbonyl, —O—Si(C₁-C₆-alkyl)₃ and non-aromatic 3- to         7-membered monocyclic heterocycle,     -   L^(Sc) is selected from the group consisting of halogen, cyano,         nitro, hydroxyl, formyl, carboxyl, oxo, methylidene,         halomethylidene, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy,         C₁-C₆-haloalkoxy, C₂-C₆-alkenyl, C₃-C₈-cycloalkyl,         C₃-C₈-halocycloalkyl, —O—Si(C₁-C₆-alkyl)₃ and non-aromatic 3- to         7-membered monocyclic heterocycle, and/or two L^(Sc)         substituents form, together with the carbon atom to which they         are attached to, a C₃-C₈-cycloalkyl;     -   R⁶ is selected from the group consisting of non-aromatic         C₃-C₁₂-carbocycle, aromatic C₆-C₁₄-carbocycle, non-aromatic 3-         to 14-membered heterocycle, aromatic 5- to 14-membered         heterocycle, non-aromatic C₃-C₁₂-carbocyclyloxy, aromatic         C₆-C₁₄-carbocyclyloxy, aromatic 5- to 14-membered         heterocyclyloxy, non-aromatic 5- to 14-membered heterocyclyloxy,         non-aromatic C₃-C₁₂-carbocyclylsulfanyl, aromatic         C₆-C₁₄-carbocyclylsulfanyl, aromatic 5- to 14-membered         heterocyclylsulfanyl, non-aromatic 5- to 14-membered         heterocyclylsulfanyl, non-aromatic C₃-C₁₂-carbocyclylsulfinyl,         aromatic C₆-C₁₄-carbocyclylsulfinyl, aromatic 5- to 14-membered         heterocyclylsulfinyl, non-aromatic 5- to 14-membered         heterocyclylsulfinyl, non-aromatic C₃-C₁₂-carbocyclylsulfonyl,         aromatic C₆-C₁₄-carbocyclylsulfonyl, aromatic 5- to 14-membered         heterocyclylsulfonyl, non-aromatic 5- to 14-membered         heterocyclylsulfonyl, C₁-C₃-alkoxy substituted by a non-aromatic         C₃-C₁₂-carbocycle, C₁-C₃-alkoxy substituted by an aromatic         C₆-C₁₄-carbocycle, C₁-C₃-alkoxy substituted by a non-aromatic 3-         to 14-membered heterocycle, C₁-C₃-alkoxy substituted by an         aromatic 5- to 14-membered heterocycle, C₁-C₃-haloalkoxy         substituted by a non-aromatic C₃-C₁₂-carbocycle,         C₁-C₃-haloalkoxy substituted by an aromatic C₆-C₁₄-carbocycle,         C₁-C₃-haloalkoxy substituted by a non-aromatic 3- to 14-membered         heterocycle, C₁-C₃-haloalkoxy substituted by an aromatic 5- to         14-membered heterocycle, C₁-C₃-sulfanyl substituted by a         non-aromatic C₃-C₁₂-carbocycle, C₁-C₃-sulfanyl substituted by an         aromatic C₆-C₁₄-carbocycle, C₁-C₃-sulfanyl substituted by a         non-aromatic 3- to 14-membered heterocycle and C₁-C₃-sulfanyl         substituted by an aromatic 5- to 14-membered heterocycle,         C₁-C₃-sulfinyl substituted by a non-aromatic C₃-C₁₂-carbocycle,         C₁-C₃-sulfinyl substituted by an aromatic C₆-C₁₄-carbocycle,         C₁-C₃-sulfinyl substituted by a non-aromatic 3- to 14-membered         heterocycle and C₁-C₃-sulfinyl substituted by an aromatic 5- to         14-membered heterocycle, C₁-C₃-sulfonyl substituted by a         non-aromatic C₃-C₁₂-carbocycle, C₁-C₃-sulfonyl substituted by an         aromatic C₆-C₁₄-carbocycle, C₁-C₃-sulfonyl substituted by a         non-aromatic 3- to 14-membered heterocycle and C₁-C₃-sulfonyl         substituted by an aromatic 5- to 14-membered heterocycle;         wherein cyclic, or cyclic moiety of, R⁶ substituents may be         substituted with one or more R^(6S) substituents that may be the         same or different,     -   R^(6S) is selected from the group consisting of halogen, cyano,         isocyano, nitro, hydroxyl, mercapto, pentafluorosulfanyl, oxo,         methylidene, halomethylidene, formyl, C₁-C₆-alkyl,         C₁-C₆-haloalkyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₂-C₆-alkenyl,         C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl,         C₂-C₆-alkenyloxy, C₂-C₆-haloalkenyloxy, C₂-C₆-alkylnyl-oxy,         C₂-C₆-haloalkylnyloxy, C₁-C₆-alkylsulfanyl,         C₁-C₆-haloalkylsulfanyl, C₃-C₈-cycloalkylsulfanyl,         C₁-C₆-alkylsulfinyl, C₁-C₆-haloalkylsulfinyl,         C₃-C₈-cycloalkylsulfinyl, C₁-C₆-alkylsulfonyl,         C₁-C₆-haloalkylsulfonyl, C₃-C₈-cycloalkylsulfonyl,         C₃-C₈-cycloalkyl, C₃-C₈-cycloalkyloxy, C₃-C₈-cycloalkenyl,         aromatic C₆-C₁₄-carbocycle, aromatic 5- or 6-membered monocyclic         heterocycle, non-aromatic 3- to 7-membered monocyclic         heterocycle, —N(R^(c))₂, O—(C═O)R^(d), —C(═O)R^(d),         —C(═O)(OR^(d)), —C(═O)N(R^(d))₂, —S(═O)₂N(R^(d))₂,         —O—Si(C₁-C₆-alkyl)₃ and —Si(C₁-C₆-alkyl)₃, or two R^(6S)         substituents may form, together with the carbon atom to which         they are attached to, a C₃-C₈-cycloalkyl,         -   with R^(c) being independently selected from the group             consisting of hydrogen, C₁-C₆-alkyl and C₃-C₈-cycloalkyl,         -   with R^(d) being independently selected from the group             consisting of hydrogen, C₁-C₆-alkyl and C₁-C₆-haloalkyl,     -   wherein aliphatic R^(6S), R^(c) and R^(d) substituents may be         substituted with one or more substituents independently selected         from the group consisting of cyano, halogen, hydroxyl,         C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, —O—Si(C₁-C₆-alkyl)₃,         —Si(C₁-C₆-alkyl)₃, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl and         non-aromatic 3- to 7-membered monocyclic heterocycle,     -   wherein cyclic or cyclic moiety of R^(6S) and cyclic R^(c)         substituents may be substituted with one or more substituents         independently selected from the group consisting of halogen,         cyano, nitro, hydroxyl, formyl, carboxyl, oxo, methylidene,         halomethylidene, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy,         C₁-C₆-haloalkoxy, C₁-C₆-alkoxycarbonyl,         C₁-C₆-haloalkoxycarbonyl, C₂—C-alkenyl, C₃-C₈-cycloalkyl and         C₃-C₈-halocycloalkyl, and/or cyclic or cyclic moiety of R^(6S)         substituents may be substituted with two substituents forming,         together with the carbon atom to which they are attached to, a         C₃-C₈-cycloalkyl;     -   R⁷ is selected from the group consisting of hydrogen, halogen,         cyano, isocyano, hydroxyl, mercapto, nitro, amino, formyl,         C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-hydroxyalkyl, C₁-C₆-alkoxy,         C₁-C₆-haloalkoxy, C₁-C₆-alkylcarbonyl, C₁-C₆-haloalkylcarbonyl,         C₁-C₆-alkoxycarbonyl, C₁-C₆-haloalkoxycarbonyl, C₂-C₆-alkenyl,         C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl,         C₂-C₆-alkenyloxy, C₂-C₆-haloalkenyloxy, C₂-C₆-alkynyloxy,         C₂-C₆-haloalkynyloxy, C₁-C₆-alkylsulfanyl,         C₁-C₆-haloalkylsulfanyl, C₃-C₈-cycloalkylsulfanyl,         C₂-C₆-alkenylsulfanyl, C₂-C₆-alkynylsulfanyl,         C₁-C₆-alkylsulfinyl, C₁-C₆-haloalkylsulfinyl,         C₃-C₈-cycloalkylsulfinyl, C₁-C₆-alkylsulfonyl,         C₁-C₆-haloalkylsulfonyl, C₃-C₈-cycloalkylsulfonyl,         C₃-C₈-cycloalkyl, C₃-C₆-cycloalkenyl, aromatic         C₆-C₁₄-carbocycle, aromatic 5- or 6-membered monocyclic         heterocycle, non-aromatic 3- to 7-membered monocyclic         heterocycle, C₃-C₈-cycloalkyloxy, aromatic         C₆-C₁₄-carbocyclyloxy, aromatic 5- or 6-membered monocyclic         heterocyclyloxy, non-aromatic 3- to 7-membered monocyclic         heterocyclyloxy, —O—Si(C₁-C₆-alkyl)₃, —Si(C₁-C₆-alkyl)₃,         —N(R^(e))₂, —C(═NR^(f))R^(f), NR^(g)C(═O)R^(g), —C(═O)(OR^(g)),         —C(═O)N(R^(g))₂, —S(═O)₂N(R^(g))₂ and —S(═O)(═NR^(g))R^(g),     -   with R^(e) being independently selected from the group         consisting of hydrogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl,         C₁-C₆-alkoxy, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl,         C₂-C₆-haloalkynyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl,         aromatic C₆-C₁₄-carbocycle, aromatic 5- or 6-membered monocyclic         heterocycle and non-aromatic 3- to 7-membered monocyclic         heterocycle,     -   with R^(f) being independently selected from the group         consisting of hydroxyl, amino, cyano, C₁-C₆-alkyl,         C₁-C₆-haloalkyl, C₁-C₆-alkoxy, C₁-C₆-alkylamino and         di(C₁-C₆-alkyl)amino,     -   with R^(g) being independently selected from the group         consisting of hydrogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl and         C₃-C₈-cycloalkyl,         wherein aliphatic R⁷, R^(e), R^(f) and R^(g) substituents may be         substituted with one or more R^(7Sa) substituents that may be         the same or different,         wherein cyclic or cyclic moiety of R⁷, cyclic R^(e) and cyclic         R^(g) substituents may be substituted with one or more R^(7Sc)         substituents that may be the same or different,     -   R^(7Sa) is selected from the group consisting of cyano,         hydroxyl, carboxyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy,         C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, C₁-C₆-alkoxycarbonyl,         —O—Si(C₁-C₆-alkyl)₃, —Si(C₁-C₆-alkyl)₃, aromatic         C₆-C₁₄-carbocycle and non-aromatic 3- to 7-membered monocyclic         heterocycle,     -   R^(7Sc) is selected from the group consisting of halogen, cyano,         nitro, hydroxyl, formyl, oxo, methylidene, halomethylidene,         C₁-C₆-alkyl, C₁-C₆-haloalkyl C₁-C₆-alkoxy, C₁-C₆-haloalkoxy,         C₂-C₆-alkenyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl,         —O—Si(C₁-C₆-alkyl)₃ and non-aromatic 3- to 7-membered monocyclic         heterocycle, or two R^(7Sc) substituents form, together with the         carbon atom to which they are attached to, a C₃-C₈-cycloalkyl;     -   R⁸ is selected from the group consisting of hydrogen, halogen,         cyano, isocyano, amino, nitro, hydroxyl, mercapto, carboxyl,         C₁-C₆-alkoxycarbonyl, C₁-C₆-alkyl, C₁-C₆-haloalkyl,         C₁-C₆-hydroxyalkyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy,         C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl,         C₂-C₆-haloalkynyl, C₂-C₆-alkenyloxy, C₂-C₆-haloalkenyloxy,         C₂-C₆-alkynyloxy, C₂-C₆-haloalkynyloxy, C₃-C₈-cycloalkyl,         C₃-C₆-cycloalkenyl, aromatic C₆-C₁₄-carbocycle, non-aromatic 3-         to 14-membered heterocycle, aromatic 5- to 14-membered         heterocycle, C₃-C₈-cycloalkyloxy, aromatic         C₆-C₁₄-carbocyclyloxy, non-aromatic 3- to 14-membered         heterocyclyloxy, aromatic 5- to 14-membered heterocyclyloxy,         —O—Si(C₁-C₆-alkyl)₃, —Si(C₁-C₆-alkyl)₃, —N(R^(h))₂, —SR^(i),         —S(═O)R^(i) and —S(═O)₂R^(i),     -   with R^(h) being independently selected from the group         consisting of hydrogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl,         C₁-C₆-alkoxy, C₂-C₆alkenyl, C₂-C₆haloalkenyl, C₂-C₆-alkynyl,         C₂-C₆-haloalkynyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl,         aromatic C₆-C₁₄-carbocycle, aromatic 5- to 14-membered         heterocycle and non-aromatic 3- to 7-membered monocyclic         heterocycle,     -   with R^(i) being selected from the group consisting of         C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₂-C₆-alkenyl, C₂-C₆ haloalkenyl,         C₂-C₆-alkynyl, C₂-C₆-haloalkynyl, C₃-C₈-cycloalkyl,         C₃-C₈-halocycloalkyl, aromatic C₆-C₁₄-carbocycle, aromatic 5- to         14-membered heterocycle and non-aromatic 3- to 7-membered         monocyclic heterocycle,         wherein aliphatic R⁸, R^(h) and R^(i) substituents may be         substituted with one or more R^(8Sa) substituents that may be         the same or different,         wherein cyclic or cyclic moiety of R⁸, cyclic R^(h) and cyclic         R^(i) substituents may be substituted with one or more R^(8Sc)         substituents that may be the same or different,     -   R^(8Sa) is selected from the group consisting of cyano, amino,         nitro, hydroxyl, formyl, carboxyl, C₁-C₆-alkoxy,         C₁-C₆-haloalkoxy, C₁-C₆-alkoxy-C₁-C₆-alkoxy,         C₁-C₆-alkoxycarbonyl, C₁-C₆-haloalkoxycarbonyl,         C₁-C₆-alkylcarbonyl, C₁-C₆-haloalkylcarbonyl, C₃-C₈-cycloalkyl,         C₃-C₈-halocycloalkyl, C₁-C₆-alkylsulfanyl,         C₁-C₆-haloalkylsulfanyl, C₁-C₆-alkylsulfinyl,         C₁-C₆-haloalkylsulfinyl, C₁-C₆-alkylsulfonyl,         C₁-C₆-haloalkylsulfonyl, —O—Si(C₁-C₆-alkyl)₃, —Si(C₁-C₆-alkyl)₃,         non-aromatic 3- to 7-membered monocyclic heterocycle and         —N(R^(a′))₂ with R^(a′) being independently selected from the         group consisting of hydrogen, formyl, C₁-C₆-alkyl,         C₁-C₆-haloalkyl, C₃-C₈-cycloalkyl and C₁-C₆-alkylcarbonyl,         wherein said non-aromatic 3- to 7-membered monocyclic         heterocycle R^(8Sa) may be substituted with one or more         C₁-C₆-alkyl substituents that may be the same or different,     -   R^(8Sc) is selected from the group consisting of halogen, cyano,         amino, nitro, hydroxyl, formyl, carboxyl, oxo, methylidene,         halomethylidene, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy,         C₁-C₆-haloalkoxy, C₁-C₆-alkoxycarbonyl,         C₁-C₆-haloalkoxycarbonyl, C₂-C₆-alkenyl, C₁-C₆-alkylsulfanyl,         C₁-C₆-alkylsulfinyl, C₁-C₆-alkylsulfonyl, C₃-C₈-cycloalkyl,         C₃-C₈-halocycloalkyl, —O—Si(C₁-C₆-alkyl)₃ and non-aromatic 3- to         7-membered monocyclic heterocycle that may be substituted with         one or more C₁-C₆-alkyl substituents that may be the same or         different, or two R^(8Sc) substituents form, together with the         carbon atom to which they are attached to, a C₃-C₈-cycloalkyl or         a non-aromatic 3- to 7-membered monocyclic heterocycle, wherein         said non-aromatic 3- to 7-membered monocyclic heterocycle may be         substituted with one or more C₁-C₆-alkyl substituents that may         be the same or different;     -   Q is selected from the group consisting of aromatic         C₆-C₁₄-carbocycle, non-aromatic C₃-C₁₂-carbocycle, non-aromatic         3- to 14-membered heterocycle and aromatic 5- to 14-membered         heterocycle, wherein any of said carbocycle or heterocycle         groups may be substituted with one or more Q^(S) substituents         that may be the same or different,         -   Q^(S) is selected from the group consisting of halogen,             cyano, isocyano, nitro, hydroxyl, mercapto, formyl,             carboxyl, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkylcarbonyl,             C₁-C₆-haloalkylcarbonyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy,             C₁-C₆-alkoxycarbonyl, C₁-C₆-haloalkoxycarbonyl, C₂-C₆             alkenyl, C₂-C₆-haloalkenyl, C₂—C-alkynyl, C₂-C₆-haloalkynyl,             C₂-C₆-alkenyloxy, C₂-C₆-haloalkenyloxy, C₁-C₆-alkylsulfanyl,             C₁-C₆-haloalkylsulfanyl, C₁-C₆-alkylsulfinyl,             C₁-C₆-haloalkylsulfinyl, C₁-C₆-alkylsulfonyl,             C₁-C₆-haloalkylsulfonyl, C₃-C₈-cycloalkyl,             C₃-C₈-cycloalkyloxy, C₃-C₆-cycloalkenyl, non-aromatic 3- to             7-membered monocyclic heterocycle, aromatic             C₆-C₁₄-carbocycle, aromatic 5- to 14-membered heterocycle,             —O—Si(C₁-C₆-alkyl)₃, —Si(C₁-C₆-alkyl)₃, —O—C(═O)R^(j),             —NR^(j)C(═O)R^(j), —C(═O)N(R^(j))₂, —C(═S)R^(j),             —C(═S)N(R^(j))₂, —C(═NR^(j))R^(j) and —C(═NOR^(j))R^(j) and             —N(R^(k))₂             -   with R^(j) being independently selected from the group                 consisting of hydrogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl and                 C₁-C₆-alkoxy,             -   with R^(k) being independently selected from the group                 consisting of hydrogen, hydroxyl, C₁-C₆-alkyl,                 C₁-C₆-haloalkyl, C₁-C₆-alkoxy, C₂-C₆-alkenyl,                 C₂-C₆-haloalkenyl and C₃-C₈-cycloalkyl,         -   wherein aliphatic Q^(S), R^(j) and R^(k) substituents may be             substituted with one or more substituents independently             selected from the group consisting of cyano, amino, nitro,             hydroxyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy,             C₁-C₆-alkoxycarbonyl, C₁-C₆-haloalkoxycarbonyl,             C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, —Si(C₁-C₆-alkyl)₃             and non-aromatic 3- to 7-membered monocyclic heterocycle,     -   wherein cyclic or cyclic moiety of Q^(S) and cyclic R^(k)         substituents may be substituted with one or more R^(Qs)         substituents independently selected from the group consisting of         halogen, cyano, amino, nitro, hydroxyl, formyl, carboxyl, oxo,         methylidene, halomethylidene, C₁-C₆-alkyl, C₁-C₆-haloalkyl,         C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₁-C₆-alkoxycarbonyl,         C₁-C₆-haloalkoxycarbonyl, C₃-C₈-cycloalkyl,         C₃-C₈-halocycloalkyl, C₂-C₆-alkenyl and non-aromatic 3- to         7-membered monocyclic heterocycle, wherein cyclic R^(Qs)         substituents may be substituted with two substituents forming,         together with the carbon atom to which they are attached to, a         C₃-C₈-cycloalkyl,         and     -   (B) at least one further active compound selected from         -   (1) inhibitors of the ergosterol synthesis,         -   (2) inhibitors of the respiratory chain at complex I or II,         -   (3) inhibitors of the respiratory chain at complex III,         -   (4) inhibitors of the mitosis and cell division,         -   (5) compounds capable of having a multisite action,         -   (6) compounds capable of inducing a host defense,         -   (7) inhibitors of the amino acid and/or protein             biosynthesis,         -   (8) inhibitors of the ATP production,         -   (9) inhibitors of the cell wall synthesis,         -   (10) inhibitors of the lipid and membrane synthesis,         -   (11) inhibitors of the melanine biosynthesis,         -   (12) inhibitors of the nucleic acid synthesis,         -   (13) inhibitors of the signal transduction,         -   (14) compounds capable of acting as uncoupler,         -   (15) other fungicides,         -   (16) antibacterial agents         -   (17) biological fungicides         -   (18) fatty acids or derivatives thereof.

Compound (A)

The active compound combinations according to the invention comprise as compound (A) at least one compound of formula (I) or a salt or N-oxide thereof.

In a preferred embodiment compounds according to the present invention are compounds of formula (I), wherein

-   -   A is selected from the group consisting of O, S, C(═O), S(═O),         S(═O)₂, NR¹ and CR¹R², with R¹ and R² being independently         selected from the group consisting of hydrogen, C₁-C₄-alkyl and         C₃-C₆-cycloalkyl,     -   m is 0, 1 or 2;     -   T is selected from the group consisting of hydrogen and         C₁-C₄-alkyl,     -   R³ and R⁴ are independently selected from the group consisting         of hydrogen, fluorine, chlorine, C₁-C₄-alkyl, C₂-C₄-alkenyl,         C₂-C₄-alkynyl, C₃-C₈-cycloalkyl,     -   R⁵ is selected from the group consisting of hydrogen, hydroxyl,         C₁-C₄-alkyl, C₁-C₄-alkoxy, C₁-C₄-alkylsulfanyl,         wherein aliphatic R¹, R², R³, R⁴ and R⁵ substituents may be         substituted with one to three substituents independently         selected from the group consisting of fluorine, chlorine,         C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₃-C₆-cycloalkyl,         C₃-C₆-halocycloalkyl,         wherein cyclic R¹, R², R³, R⁴ and R⁵ substituents may be         substituted with one to three substituents independently         selected from the group consisting of fluorine, chlorine oxo,         methylidene, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy,         C₁-C₄-haloalkoxy, C₂-C₄-alkenyl, C₃-C₆-cycloalkyl,         C₃-C₆-halocycloalkyl,     -   R³ or R⁴, and R⁵ may form, together with the carbon atom to         which they are attached to, a C₃-C₆-cycloalkyl;     -   L represents a direct bond or L is selected from the group         consisting of C₁-C₆-alkylene, C₁-C₆-alkylene substituted on a         same carbon atom by two substituents forming together with the         carbon atom to which they are attached to a C₃-C₆-cycloalkyl,         C₁-C₆-alkylene substituted on a same carbon atom by two         substituents forming together with the carbon atom to which they         are attached to a non-aromatic 3- to 7-membered monocyclic         heterocycle,         wherein aliphatic L substituents may be substituted with one to         three L^(Sa) substituents independently selected from the group         consisting of fluorine, chlorine, hydroxyl, C₁-C₄-alkoxy,         C₁-C₄-haloalkoxy, C₃-C₆-cycloalkyl and C₃-C₆-halocycloalkyl,         wherein cyclic or cyclic moiety of L substituents may be         substituted with one to three L^(Sc) substituents independently         selected from the group consisting of fluorine, chlorine,         hydroxyl, oxo, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy,         C₁-C₄-haloalkoxy, C₂-C₄alkenyl, C₃-C₆-cycloalkyl and         C₃-C₆-halocycloalkyl,     -   R⁶ is selected from the group consisting of non-aromatic         C₃-C₁₂-carbocycle, aromatic C₆-C₁₄-carbocycle, non-aromatic 3-         to 14-membered heterocycle, aromatic 5- to 14-membered         heterocycle, non-aromatic C₃-C₁₂-carbocyclyloxy, aromatic         C₆-C₁₄-carbocyclyloxy, aromatic 5- to 14-membered         heterocyclyloxy, non-aromatic 5- to 14-membered heterocyclyloxy,         non-aromatic C₃-C₁₂-carbocyclylsulfanyl, aromatic         C₆-C₁₄-carbocyclylsulfanyl, aromatic 5- to 14-membered         heterocyclylsulfanyl and non-aromatic 5- to 14-membered         heterocyclylsulfanyl,         wherein cyclic, or cyclic moiety of, R⁶ substituents may be         substituted with one to three R^(6S) substituents that may be         the same or different,     -   R^(6S) is selected from the group consisting of halogen, cyano,         nitro, hydroxyl, mercapto, pentafluorosulfanyl, oxo,         methylidene, halomethylidene, C₁-C₆-alkyl, C₁-C₆-haloalkyl,         C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₂-C₆-alkenyl,         C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl,         C₁-C₆-alkylsulfanyl, C₁-C₆-haloalkylsulfanyl,         C₃-C₆-cycloalkylsulfanyl, C₃-C₆-cycloalkyl, C₃-C₆-cycloalkyloxy,         phenyl, naphthyl aromatic 5- or 6-membered monocyclic         heterocycle, non-aromatic 3- to 7-membered monocyclic         heterocycle, —C(═O)(OR^(d)) and —C(═O)N(R^(d))₂,         -   with R^(d) being independently selected from the group             consisting of hydrogen, C₁-C₄-alkyl and C₁-C₄-haloalkyl,     -   wherein aliphatic R^(6S), R^(c) and R^(d) substituents may be         substituted with one to three substituents independently         selected from the group consisting of fluorine, chlorine         hydroxyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₃-C₆-cycloalkyl and         C₃-C₆-halocycloalkyl, wherein cyclic or cyclic moiety of R^(6S)         and cyclic R^(c) substituents may be substituted with one to         three substituents independently selected from the group         consisting of fluorine, chlorine C₁-C₄-alkyl, C₁-C₄-haloalkyl,         C₁-C₄-alkoxy and C₁-C₄-haloalkoxy,     -   R⁷ is selected from the group consisting of hydrogen, halogen,         cyano, hydroxyl, mercapto, C₁-C₄-alkyl, C₁-C₄-haloalkyl,         C₁-C₄-hydroxyalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy,         C₁-C₄-alkylcarbonyl, C₁-C₄-haloalkylcarbonyl, C₂-C₄-alkenyl,         C₂-C₄-haloalkenyl, C₂-C₄-alkynyl, C₂-C₄-haloalkynyl,         C₁-C₄-alkylsulfanyl, C₁-C₄-haloalkylsulfanyl,         C₃-C₆-cycloalkylsulfanyl, C₁-C₄-alkylsulfinyl,         C₁-C₄-haloalkylsulfinyl, C₃-C₆-cycloalkylsulfinyl,         C₁-C₄-alkylsulfonyl, C₁-C₄-haloalkylsulfonyl,         C₃-C₆-cycloalkylsulfonyl, C₃-C₆-cycloalkyl, C₃-C₆-cycloalkenyl,         phenyl, naphthyl, aromatic 5- or 6-membered monocyclic         heterocycle, non-aromatic 3- to 7-membered monocyclic         heterocycle, C₃-C₈-cycloalkyloxy, aromatic         C₆-C₁₄-carbocyclyloxy, aromatic 5- or 6-membered monocyclic         heterocyclyloxy, non-aromatic 3- to 7-membered monocyclic         heterocyclyloxy, —N(R^(e))₂, —C(═NR^(f))R^(f), NR^(g)C(═O)R^(g),         —C(═O)(OR^(g)), —C(═O)N(R^(g))₂, —S(═O)₂N(R^(g))₂ and         —S(═O)(═NR^(g))R^(g),     -   with R^(e) being independently selected from the group         consisting of hydrogen, C₁-C₄-alkyl, C₁-C₄-haloalkyl,         C₂-C₄-alkenyl, C₂-C₄-haloalkenyl, C₂-C₄-alkynyl,         C₂-C₄-haloalkynyl, C₃-C₆-cycloalkyl, C₃-C₆-halocycloalkyl,     -   with R^(f) being independently selected from the group         consisting of hydroxyl, C₁-C₄-alkyl, C₁-C₄-haloalkyl,         C₁-C₄-alkoxy,     -   with R^(g) being independently selected from the group         consisting of hydrogen, C₁-C₄-alkyl, C₁-C₄-haloalkyl and         C₃-C₆-cycloalkyl,         wherein aliphatic R⁷, R^(e), R^(f) and R^(g) substituents may be         substituted with one to three R^(7Sa) substituents that may be         the same or different,         wherein cyclic or cyclic moiety of R⁷, cyclic R^(e) and cyclic         R^(g) substituents may be substituted with one to three R^(7Sc)         substituents that may be the same or different,     -   R^(7Sa) is selected from the group consisting of hydroxyl,         C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₃-C₆-cycloalkyl, R^(7Sc) is         selected from the group consisting of fluorine, chlorine         hydroxyl, oxo, C₁-C₄-alkyl, C₁-C₄-haloalkyl C₁-C₄-alkoxy,         C₁-C₄-haloalkoxy, C₃-C₆-cycloalkyl,     -   R⁸ is selected from the group consisting of hydrogen, halogen,         amino, hydroxyl, mercapto, C₁-C₄-alkyl, C₁-C₄-haloalkyl,         C₁-C₄-hydroxyalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy,         C₂-C₄-alkenyl, C₂-C₄-haloalkenyl, C₂-C₄-alkynyl,         C₂-C₄-haloalkynyl, C₂-C₄-alkenyloxy, C₂-C₄-haloalkenyloxy,         C₂-C₄-alkynyloxy, C₂-C₄-haloalkynyloxy, C₃-C₆-cycloalkyl,         C₃-C₈-cycloalkenyl, phenyl, naphthyl, non-aromatic 3- to         7-membered heterocycle, aromatic 5- or 6-membered heterocycle,         C₃-C₈-cycloalkyloxy, phenyloxy, naphthyloxy, non-aromatic 3- to         7-membered heterocyclyloxy, aromatic 5- or 6-membered         heterocyclyloxy, —N(R^(h))₂, —SR^(i), —S(═O)R^(i) and         —S(═O)₂R^(i),     -   with R^(h) being independently selected from the group         consisting of hydrogen, C₁-C₄-alkyl, C₁-C₄-haloalkyl,         C₂-C₄alkenyl, C₂-C₄haloalkenyl, C₃-C₆-cycloalkyl,         C₃-C₆-halocycloalkyl, phenyl, naphthyl aromatic 5- or 6-membered         heterocycle and non-aromatic 3- to 7-membered monocyclic         heterocycle,     -   with R^(i) being selected from the group consisting of         C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₂-C₄-alkenyl, C₂-C₄-haloalkenyl,         C₂-C₄-alkynyl, C₂-C₄-haloalkynyl, C₃-C₆-cycloalkyl,         C₃-C₆-halocycloalkyl, phenyl, naphthyl, aromatic 5- or         6-membered heterocycle and non-aromatic 3- to 7-membered         monocyclic heterocycle,         wherein aliphatic R^(g), R^(h) and R^(i) substituents may be         substituted with one to three R^(8Sa) substituents that may be         the same or different,         wherein cyclic or cyclic moiety of R⁸, cyclic R^(h) and cyclic         R^(i) substituents may be substituted with one to three R^(8Sc)         substituents that may be the same or different,     -   R^(8Sa) is selected from the group consisting of hydroxyl,         carboxyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₁-C₄-alkoxycarbonyl,         C₁-C₄-haloalkoxycarbonyl, C₃-C₆-cycloalkyl,         C₃-C₆-halocycloalkyl, C₁-C₄-alkylsulfanyl,         C₁-C₄-haloalkylsulfanyl, C₁-C₄-alkylsulfinyl,         C₁-C₄-haloalkylsulfinyl, C₁-C₄-alkylsulfonyl,         C₁-C₄-haloalkylsulfonyl,—and non-aromatic 3- to 7-membered         monocyclic heterocycle, wherein said non-aromatic 3- to         7-membered monocyclic heterocycle R^(8Sa) may be substituted         with one or two C₁-C₄-alkyl substituents that may be the same or         different,     -   R^(8Sc) is selected from the group consisting of halogen, oxo,         C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy and         C₃-C₆-cycloalkyl,     -   Q is selected from the group consisting of phenyl, naphthyl,         non-aromatic C₅-C₁₀-carbocycle, non-aromatic 5- to 10-membered         heterocycle and aromatic 5- to 10-membered heterocycle, wherein         any of said carbocycle or heterocycle groups may be substituted         with one to three Q^(S) substituents that may be the same or         different,         -   Q^(S) is selected from the group consisting of halogen,             cyano, nitro, formyl, carboxyl, C₁-C₄-alkyl,             C₁-C₄-haloalkyl, C₁-C₄-alkylcarbonyl,             C₁-C₄-haloalkylcarbonyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy,             C₁-C₄-alkoxycarbonyl, C₁-C₄-haloalkoxycarbonyl,             C₂-C₄alkenyl, C₂-C₄haloalkenyl, C₂-C₄-alkynyl,             C₂-C₄-haloalkynyl, C₁-C₄-alkylsulfanyl,             C₁-C₄-haloalkylsulfanyl, C₁-C₄-alkylsulfinyl,             C₁-C₄-haloalkylsulfinyl, C₁-C₄-alkylsulfonyl,             C₁-C₄-haloalkylsulfonyl, C₃-C₆-cycloalkyl, non-aromatic 3-             to 7-membered monocyclic heterocycle, phenyl, naphthyl and             aromatic 5- to 10-membered heterocycle,         -   wherein aliphatic Q^(S), R^(j) and R^(k) substituents may be             substituted with one to three substituents independently             selected from the group consisting of hydroxyl,             C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₃-C₆-cycloalkyl and             C₃-C₆-halocycloalkyl, wherein cyclic or cyclic moiety of             Q^(S) and cyclic R^(k) substituents may be substituted with             one to three R^(Qs) substituents independently selected from             the group consisting of fluorine, chlorine, C₁-C₄-alkyl,             C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy and             C₃-C₆-cycloalkyl.

In a more preferred embodiment compounds according to the present invention are compounds of formula (I), wherein

-   -   A is selected from the group consisting of O, S(═O)₂, NR¹ and         CR¹R², with R¹ and R² being independently selected from the         group consisting of hydrogen, C₁-C₄-alkyl and C₃-C₆-cycloalkyl,     -   m is 0, 1 or 2;     -   T is selected from the group consisting of hydrogen and         C₁-C₄-alkyl,     -   R³ and R⁴ are independently selected from the group consisting         of hydrogen, fluorine, chlorine, C₁-C₄-alkyl, C₂-C₄-alkenyl,         C₂-C₄-alkynyl and C₃-C₆-cycloalkyl,     -   R⁵ is selected from the group consisting of hydrogen, hydroxyl,         C₁-C₄-alkyl and C₁-C₄-alkoxy,     -   L represents a direct bond or L is selected from the group         consisting of C₁-C₆-alkylene,         wherein aliphatic L substituents may be substituted with one to         three L^(Sa) substituents independently selected from the group         consisting of fluorine, chlorine, hydroxyl, C₁-C₄-alkoxy,         C₁-C₄-haloalkoxy and C₃-C₆-cycloalkyl,         wherein cyclic or cyclic moiety of L substituents may be         substituted with one to three L^(Sc) substituents independently         selected from the group consisting of fluorine, chlorine,         hydroxyl, oxo, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy,         C₁-C₄-haloalkoxy and C₃-C₆-cycloalkyl,     -   R⁶ is selected from the group consisting of non-aromatic         C₅-C₁₀-carbocycle, phenyl, naphthyl, non-aromatic 5- to         10-membered heterocycle, aromatic 5- to 10-membered heterocycle,         non-aromatic C₅-C₁₀-carbocyclyloxy, phenoxy, naphthyloxy,         aromatic 5- to 10-membered heterocyclyloxy, non-aromatic 5- to         10-membered heterocyclyloxy and phenylsulfanyl,         wherein cyclic, or cyclic moiety of R⁶ substituents may be         substituted with one to three R^(6S) substituents independently         selected from the group consisting of halogen, nitro, hydroxyl,         C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy,         C₂-C₄-alkenyl, C₂-C₄-alkynyl, C₁-C₄-haloalkylsulfanyl,         cyclopropyl, cyclobutyl, cyclopentyl, pyridinyl, oxetanyl and         tetrahydrofuranyl, wherein cyclic R^(6S) substituents may be         substituted with one or two substituents independently selected         from the group consisting of halogen, C₁-C₄-alkyl,         C₁-C₄-haloalkyl and C₁-C₄-alkoxycarbonyl,     -   R⁷ is selected from the group consisting of hydrogen, halogen,         cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-hydroxyalkyl,         C₁-C₄-alkylcarbonyl, C₁-C₄-alkoxy, C₂-C₄-alkenyl, C₂-C₄-alkynyl,         C₁-C₄-alkylsulfanyl, C₁-C₄-alkenylsulfanyl, C₁-C₄-alkylsulfonyl,         C₃-C₈-cycloalkyl, pyridinyl, imidazolyl, pyrazolyl, thiazolyl,         oxetanyl, tetrahydrofuranyl, pyrrolidinyl, —N(R^(e))₂,         —C(═NR^(f))R^(f) and —C(═O)N(R^(g))₂,     -   with R^(e) being independently selected from the group         consisting of hydrogen, C₁-C₄-alkyl and C₃-C₆-cycloalkyl,     -   with R^(f) being independently selected from the group         consisting of C₁-C₄-alkyl and C₁-C₄-alkoxy,     -   with R^(g) being independently selected from the group         consisting of hydrogen, C₁-C₄-alkyl and C₃-C₆-cycloalkyl,         wherein said aliphatic R⁷, R^(e) and R^(g) substituents may be         substituted with one to three R^(7Sa) substituents independently         selected from the group consisting of hydroxyl, C₁-C₄-alkoxy and         C₃-C₆-cycloalkyl,         wherein said cyclic R⁷, R^(e) and R^(g) substituents may be         substituted with one to three R^(7Sc) substituents independently         selected from the group consisting of halogen, hydroxyl,         C₁-C₄-alkyl and C₁-C₄-alkoxy,     -   R⁸ is selected from the group consisting of hydrogen, halogen,         hydroxyl, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy,         C₂-C₄-alkenyl, C₁-C₄-alkylsulfanyl, C₁-C₄-haloalkylsulfanyl,         C₁-C₄-alkylsulfinyl, C₁-C₄-alkylsulfonyl, C₃-C₆-cycloalkyl,         phenyl, naphthyl, oxetanyl, azetidinyl, tetrahydrofuranyl,         pyrrolidinyl, tetrahydropyranyl, piperidinyl, piperazinyl,         morpholinyl, furanyl, thienyl, pyrrolyl, pyrazolyl, thiazolyl,         imidazolyl, oxazolyl, isoxazolyl, pyridinyl, pyrimidinyl,         C₃-C₆-cycloalkyloxy and —N(R^(h))₂,     -   with R^(h) being independently selected from the group         consisting of hydrogen, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₂-C₄         alkenyl, C₃-C₆-cycloalkyl, phenyl, oxetanyl, azetidinyl,         pyrrolidinyl and tetrahydrofuranyl,         wherein aliphatic R⁸ and R^(h) substituents as disclosed herein         may be substituted with one or two R^(8Sa) substituents         independently selected from the group consisting of hydroxyl,         C₁-C₄-alkoxy, C₁-C₄-alkoxycarbonyl, C₃-C₆-cycloalkyl,         C₁-C₄-alkylsulfanyl oxetanyl, azetidinyl, pyrrolidinyl and         tetrahydrofuranyl,         wherein cyclic R⁸ and R^(h) substituents as disclosed herein may         be substituted with one or two R^(8Sc) substituents         independently selected from the group consisting of oxo,         fluorine, chlorine, hydroxyl, C₁-C₄-alkyl, C₁-C₄-haloalkyl,         C₁-C₄-alkoxy, C₃-C₆-cycloalkyl, oxetanyl, azetidinyl,         pyrrolidinyl and tetrahydrofuranyl     -   Q is selected from the group consisting of phenyl,         1,3-benzodioxol-5-yl, 2,3-dihydrobenzofuranyl, pyridinyl,         thien-yl and indol-5-yl,         wherein more preferred Q groups as disclosed herein may be         substituted with one or two Q^(S) substituents independently         selected from the group consisting of halogen, cyano, nitro,         formyl, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy,         C₁-C₄-haloalkoxy, C₂-C₄alkenyl, C₂-C₄-alkynyl,         C₁-C₄-alkylsulfanyl, C₃-C₆-cycloalkyl and non-aromatic 3- to         7-membered monocyclic heterocycle,     -   wherein said more preferred aliphatic Q^(S) substituents may be         substituted with one or two substituents independently selected         from the group consisting of hydroxyl, C₁-C₄-alkoxy,         C₁-C₄-haloalkoxy, C₁-C₄-alkoxycarbonyl, C₁-C₄-haloalkoxycarbonyl         and C₃-C₆-cycloalkyl.

In an even more preferred embodiment compounds according to the present invention are compounds of formula (I), wherein

A is selected from the group consisting of O, NR¹ and CR¹R², with R¹ and R² being independently selected from the group consisting of hydrogen, methyl or ethyl,

-   -   m is 1;     -   T is hydrogen,     -   R³ and R⁴ are independently selected from the group consisting         of hydrogen or fluorine,     -   R⁵ is hydrogen,     -   L represents a direct bond or L is methylene,         -   R⁶ is indanyl, 1,2,3,4-tetrahydronaphthalenyl, phenyl,             naphthyl, 2,3-dihydrobenzofuranyl,             2,3-dihydro-1,4-benzodioxinyl, thienyl, pyridinyl, indolyl,             benzofuranyl, benzothiophenyl or phenoxy,             wherein cyclic, or cyclic moiety of R⁶ substituents may be             substituted with one or two R^(6S) substituents that may be             the same or different,     -   R^(6S) is selected from the group consisting of halogen, cyano,         C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy,         C₂-C₄-alkenyl, C₂-C₄-alkynyl, C₁-C₄-haloalkylsulfanyl,         C₃-C₈-cycloalkyl pyridinyl, oxetanyl and tetrahydrofuranyl     -   R⁷ is selected from the group consisting of halogen, cyano,         C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-hydroxyalkyl, C₁-C₄-alkoxy,         C₁-C₄-alkylcarbonyl, C₃-C₆-cycloalkyl, imidazolyl, pyrazolyl,         thiazolyl and pyridinyl,         wherein aliphatic R⁷, substituents may be substituted with one         or two R^(7Sa) substituents independently selected from the         group consisting of hydroxyl, methoxy, ethoxy and cyclopropyl,         wherein cyclic or cyclic moiety of R⁷ substituents may be         substituted with one or two R^(7Sc) substituents independently         selected from the group consisting of fluorine, methyl, ethyl         and cyclopropyl,     -   R⁸ is selected from the group consisting of hydrogen, halogen,         C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₃-C₆-cycloalkyloxy         and —N(R^(h))₂,     -   with R^(h) being independently selected from the group         consisting of hydrogen, C₁-C₄-alkyl, C₁-C₄-haloalkyl,         C₂-C₄alkenyl, and C₃-C₆-cycloalkyl,         wherein aliphatic R⁸ and R^(h) substituents may be substituted         with one or two R^(8Sa) substituents independently selected from         the group consisting of hydroxyl, methoxy and ethoxy,         wherein cyclic or cyclic moiety of R⁸ and cyclic R^(h)         substituents may be substituted with one or two R^(8Sc)         substituents independently selected from the group consisting of         fluorine, methyl, ethyl and cyclopropyl,     -   Q is selected from the group consisting of phenyl,         3-bicyclo[4.2.0]octa-1,3,5-trienyl, pyrazolyl, thiazolyl,         thienyl and pyridinyl,         wherein any of said carbocycle or heterocycle groups may be         substituted with one to three Q^(S) substituents that may be the         same or different,     -   Q^(S) is selected from the group consisting of halogen, cyano,         nitro, formyl, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy,         C₁-C₄-haloalkoxy, C₂-C₄alkenyl, C₂-C₄-alkynyl,         C₁-C₄-alkylsulfanyl C₃-C₈-cycloalkyl, oxiranyl and oxetanyl.

In a still even more preferred embodiment compounds according to the present invention are compounds of formula (I), wherein

A is O,

-   -   m is 1;     -   T is hydrogen,     -   R³ and R⁴ are hydrogen,     -   R⁵ is hydrogen,     -   L is methylene,         -   R⁶ is 2,4-dimethylphenyl, 2-methyl-4-bromophenyl or             2-chloro-4-methylphenyl,     -   R⁷ is methyl,     -   R⁸ is hydrogen,     -   Q is 2-fluoro-3-chlorophenyl, 2-fluor-3-bromophenyl or         2-fluoro-3-cyclopropylphenyl.

Still even more preferred compound combinations according to the invention comprise (A) a compound of formula (I) selected from the group consisting of (I-052) rac-3-[3-(3-cyclopropyl-2-fluorophenoxy)-6-methylpyridazin-4-yl]-5-[(2,4-dimethylphenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazine, (I-130) (5S)-3-[3-(3-cyclopropyl-2-fluorophenoxy)-6-methylpyridazin-4-yl]-5-(2,4-dimethylbenzyl)-5,6-dihydro-4H-1,2,4-oxadiazine, (I-300) rac-5-[(4-bromo-2-methylphenyl)methyl]-3-[3-(3-chloro-2-fluorophenoxy)-6-methylpyridazin-4-yl]-5,6-dihydro-4H-1,2,4-oxadiazine, (I-302) rac-3-[3-(3-chloro-2-fluorophenoxy)-6-methylpyridazin-4-yl]-5-[(2-chloro-4-methylphenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazine, (I-337) (5S)-5-[(4-bromo-2-methylphenyl)methyl]-3-[3-(3-chloro-2-fluorophenoxy)-6-methylpyridazin-4-yl]-5,6-dihydro-4H-1,2,4-oxadiazine, (I-338) (5R)-3-[3-(3-chloro-2-fluorophenoxy)-6-methylpyridazin-4-yl]-5-(2-chloro-4-methylbenzyl)-5,6-dihydro-4H-1,2,4-oxadiazine and (I-339) (5S)-3-[3-(3-chloro-2-fluoro-phenoxy)-6-methylpyridazin-4-yl]-5-(2-chloro-4-methylbenzyl)-5,6-dihydro-4H-1,2,4-oxadiazine.

Likewise still even more preferred compound combinations according to the invention comprise (A) a compound of formula (I) selected from the group consisting of (I-052) rac-3-[3-(3-cyclopropyl-2-fluorophenoxy)-6-methylpyridazin-4-yl]-5-[(2,4-dimethylphenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazine, (I-130) (5S)-3-[3-(3-cyclopropyl-2-fluorophenoxy)-6-methylpyridazin-4-yl]-5-(2,4-dimethylbenzyl)-5,6-dihydro-4H-1,2,4-oxadiazine, (I-300) rac-5-[(4-bromo-2-methylphenyl)methyl]-3-[3-(3-chloro-2-fluorophenoxy)-6-methylpyridazin-4-yl]-5,6-dihydro-4H-1,2,4-oxadiazine, (I-302) rac-3-[3-(3-chloro-2-fluorophenoxy)-6-methylpyridazin-4-yl]-5-[(2-chloro-4-methylphenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazine, (I-337) (5S)-5-[(4-bromo-2-methylphenyl)methyl]-3-[3-(3-chloro-2-fluorophenoxy)-6-methylpyridazin-4-yl]-5,6-dihydro-4H-1,2,4-oxadiazine and (I-339) (5S)-3-[3-(3-chloro-2-fluorophenoxy)-6-methylpyridazin-4-yl]-5-(2-chloro-4-methylbenzyl)-5,6-dihydro-4H-1,2,4-oxadiazine.

Likewise most preferred compound combinations according to the invention comprise (A) a compound of formula (I) selected from the group consisting of (I-052) rac-3-[3-(3-cyclopropyl-2-fluorophenoxy)-6-methylpyridazin-4-yl]-5-[(2,4-dimethylphenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazine, (I-300) rac-5-[(4-bromo-2-methylphenyl)methyl]-3-[3-(3-chloro-2-fluorophenoxy)-6-methylpyridazin-4-yl]-5,6-dihydro-4H-1,2,4-oxadiazine and (I-302) rac-3-[3-(3-chloro-2-fluorophenoxy)-6-methylpyridazin-4-yl]-5-[(2-chloro-4-methylphenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazine.

Likewise most preferred compound combinations according to the invention comprise (A) a compound of formula (I) selected from the group consisting of (I-130) (5S)-3-[3-(3-cyclopropyl-2-fluorophenoxy)-6-methylpyridazin-4-yl]-5-(2,4-dimethylbenzyl)-5,6-dihydro-4H-1,2,4-oxadiazine, (I-337) (5S)-5-[(4-bromo-2-methylphenyl)methyl]-3-[3-(3-chloro-2-fluorophenoxy)-6-methylpyridazin-4-yl]-5,6-dihydro-4H-1,2,4-oxadiazine and (I-339) (5S)-3-[3-(3-chloro-2-fluorophenoxy)-6-methylpyridazin-4-yl]-5-(2-chloro-4-methylbenzyl)-5,6-dihydro-4H-1,2,4-oxadiazine.

Most preferred compound combinations according to the invention comprise (A) a compound of formula (I) selected from the group consisting of (I-302) rac-3-[3-(3-chloro-2-fluorophenoxy)-6-methylpyridazin-4-yl]-5-[(2-chloro-4-methylphenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazine, (I-338) (5R)-3-[3-(3-chloro-2-fluorophenoxy)-6-methylpyridazin-4-yl]-5-(2-chloro-4-methylbenzyl)-5,6-dihydro-4H-1,2,4-oxadiazine and (I-339) (5S)-3-[3-(3-chloro-2-fluorophenoxy)-6-methylpyridazin-4-yl]-5-(2-chloro-4-methylbenzyl)-5,6-dihydro-4H-1,2,4-oxadiazine.

Particularly preferred compound combinations according to the invention comprise (A) a compound of formula (I) which is (I-339) (5S)-3-[3-(3-chloro-2-fluorophenoxy)-6-methylpyridazin-4-yl]-5-(2-chloro-4-methylbenzyl)-5,6-dihydro-4H-1,2,4-oxadiazine.

Definitions

The term “halogen” as used herein refers to fluorine, chlorine, bromine or iodine atom.

The term “methylidene” as used herein refers to a CH₂ group connected to a carbon atom via a double bond.

The term “halomethylidene” as used herein refers to a CX₂ group connected to a carbon atom via a double bond, wherein X is halogen.

The term “oxo” as used herein refers to an oxygen atom which is bound to a carbon atom or sulfur atom via a double bound.

The term “formyl” as used herein refers to —CH(═O).

The term “C₁-C₆-alkyl” as used herein refers to a saturated, branched or straight hydrocarbon chain having 1, 2, 3, 4, 5 or 6 carbon atoms. Examples of C₁-C₆-alkyl include but are not limited to methyl, ethyl, propyl (n-propyl), 1-methylethyl (iso-propyl), butyl (n-butyl), 1-methylpropyl (sec-butyl), 2-methylpropyl (iso-butyl), 1,1-dimethylethyl (tert-butyl), pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 2,2-dimethylpropyl, 1-ethylpropyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, hexyl, 1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 1,1-dimethylbutyl, 1,2-dimethylbutyl, 1,3-dimethylbutyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl, 3,3-dimethylbutyl, 1-ethylbutyl, 2-ethylbutyl, 1,1,2-trimethylpropyl, 1,2,2-trimethylpropyl, 1-ethyl-1-methylpropyl and 1-ethyl-2-methylpropyl. Particularly, said hydrocarbon chain has 1, 2, 3 or 4 carbon atoms (“C₁-C₄-alkyl”), e.g. methyl, ethyl, propyl, iso-propyl, butyl, sec-butyl, iso-butyl or tert-butyl.

The term “C₁-C₆-alkylene” as used herein refers to a divalent C₁-C₆-alkyl group as defined herein. Examples of C₁-C₆-alkylene include but are not limited to —CH₂—, —CH₂—CH₂—, —CH₂—CH₂—CH₂—, —CH₂—C(CH₃)—CH₂—, —CH₂—CH₂—CH₂—CH₂—, —CH₂—C(CH₃)—CH₂—CH₂—, —CH₂—CH₂—CH₂—CH₂—CH₂— and —CH₂—CH₂—CH₂—CH₂—CH₂—CH₂—.

The term “C₂-C₆-alkenyl” or “alkanediyl” as used herein refers to an unsaturated, branched or straight hydrocarbon chain having 2, 3, 4, 5 or 6 carbon atoms and comprising at least one double bond. Examples of C₂-C₆-alkenyl include but are not limited to ethenyl (or “vinyl”), prop-2-en-1-yl (or “allyl”), prop-1-en-1-yl, but-3-enyl, but-2-enyl, but-1-enyl, pent-4-enyl, pent-3-enyl, pent-2-enyl, pent-1-enyl, hex-5-enyl, hex-4-enyl, hex-3-enyl, hex-2-enyl, hex-1-enyl, prop-1-en-2-yl (or “isopropenyl”), 2-methylprop-2-enyl, 1-methylprop-2-enyl, 2-methylprop-1-enyl, 1-methylprop-1-enyl, 3-methylbut-3-enyl, 2-methylbut-3-enyl, 1-methylbut-3-enyl, 3-methylbut-2-enyl, 2-methylbut-2-enyl, 1-methylbut-2-enyl, 3-methylbut-1-enyl, 2-methylbut-1-enyl, 1-methylbut-1-enyl, 1,1-dimethylprop-2-enyl, 1-ethylprop-1-enyl, 1-propylvinyl, 1-isopropylvinyl, 4-methylpent-4-enyl, 3-methylpent-4-enyl, 2-methylpent-4-enyl, 1-methylpent-4-enyl, 4-methylpent-3-enyl, 3-methylpent-3-enyl, 2-methylpent-3-enyl, 1-methylpent-3-enyl, 4-methylpent-2-enyl, 3-methylpent-2-enyl, 2-methylpent-2-enyl, 1-methylpent-2-enyl, 4-methylpent-1-enyl, 3-methylpent-1-enyl, 2-methylpent-1-enyl, 1-methylpent-1-enyl, 3-ethylbut-3-enyl, 2-ethylbut-3-enyl, 1-ethylbut-3-enyl, 3-ethylbut-2-enyl, 2-ethylbut-2-enyl, 1-ethylbut-2-enyl, 3-ethylbut-1-enyl, 2-ethylbut-1-enyl, 1-ethylbut-1-enyl, 2-propylprop-2-enyl, 1-propylprop-2-enyl, 2-isopropylprop-2-enyl, 1-isopropylprop-2-enyl, 2-propylprop-1-enyl, 1-propylprop-1-enyl, 2-isopropylprop-1-enyl, 1-isopropylprop-1-enyl, 3,3-dimethylprop-1-enyl, 1-(1,1-dimethylethyl)ethenyl, buta-1,3-dienyl, penta-1,4-dienyl, hexa-1,5-dienyl or methylhexadienyl group.

The term “C₂-C₆-alkenylene” as used herein refers to a divalent C₂-C₆-alkenyl group as defined herein. Examples of C₂-C₆-alkenylene include but are not limited to ethenylene, propenylene, butenylene, pentenylene, hexenylene, heptenylene, octenylene, nonenylene, decenylene, undecenylene, dodecenylene, and the like.

The term “C₂-C₆-alkynyl” as used herein refers to a branched or straight hydrocarbon chain having 2, 3, 4, 5 or 6 carbon atoms and comprising at least one triple bond. Examples of C₂-C₆-alkynyl include but are not limited to ethynyl, prop-1-ynyl, prop-2-ynyl (or “propargyl”), but-1-ynyl, but-2-ynyl, but-3-ynyl, pent-1-ynyl, pent-2-ynyl, pent-3-ynyl, pent-4-ynyl, hex-1-ynyl, hex-2-ynyl, hex-3-ynyl, hex-4-ynyl, hex-5-ynyl, 1-methylprop-2-ynyl, 2-methylbut-3-ynyl, 1-methylbut-3-ynyl, 1-methylbut-2-ynyl, 3-methylbut-1-ynyl, 1-ethylprop-2-ynyl, 3-methylpent-4-ynyl, 2-methylpent-4-ynyl, 1-methyl-pent-4-ynyl, 2-methylpent-3-ynyl, 1-methylpent-3-ynyl, 4-methylpent-2-ynyl, 1-methyl-pent-2-ynyl, 4-methylpent-1-ynyl, 3-methylpent-1-ynyl, 2-ethylbut-3-ynyl, 1-ethylbut-3-ynyl, 1-ethylbut-2-ynyl, 1-propylprop-2-ynyl, 1-isopropylprop-2-ynyl, 2,2-dimethylbut-3-ynyl, 1,1-dimethylbut-3-ynyl, 1,1-dimethylbut-2-ynyl or 3,3-dimethylbut-1-ynyl group.

The term “C₂-C₆-alkynylene” as used herein refers to a divalent C₂-C₆-alkynyl group as defined herein.

The term “C₁-C₆-haloalkyl” as used herein refers to a C₁-C₆-alkyl group as defined above in which one or more hydrogen atoms are replaced with one or more halogen atoms that may be the same or different.

The term “C₂-C₆-haloalkenyl” as used herein refers to a C₂-C₆-alkenyl group as defined above in which one or more hydrogen atoms are replaced with one or more halogen atoms that may be the same or different.

The term “C₂-C₆-haloalkynyl” as used herein refers to a C₂-C₆-alkynyl group as defined above in which one or more hydrogen atoms are replaced with one or more halogen atoms that may be the same or different.

The term “C₁-C₆-alkoxy” as used herein refers to a group of formula (C₁-C₆-alkyl)-O—, in which the term “C₁-C₆-alkyl” is as defined herein. Examples of C₁-C₆-alkoxy include but are not limited to methoxy, ethoxy, n-propoxy, 1-methylethoxy, n-butoxy, 1-methylpropoxy, 2-methylpropoxy, 1,1-dimethylethoxy, n-pentoxy, 1-methylbutoxy, 2-methylbutoxy, 3-methylbutoxy, 2,2-dimethylpropoxy, 1-ethylpropoxy, 1,1-dimethylpropoxy, 1,2-dimethylpropoxy, n-hexyloxy, 1-methylpentoxy, 2-methylpentoxy, 3-methylpentoxy, 4-methylpentoxy, 1,1-dimethylbutoxy, 1,2-dimethylbutoxy, 1,3-dimethylbutoxy, 2,2-dimethylbutoxy, 2,3-dimethylbutoxy, 3,3-dimethylbutoxy, 1-ethylbutoxy, 2-ethylbutoxy, 1,1,2-trimethylpropoxy, 1,2,2-trimethylpropoxy, 1-ethyl-1-methylpropoxy and 1-ethyl-2-methylpropoxy.

The term “C₁-C₆-haloalkoxy” as used herein refers to a C₁-C₆-alkoxy group as defined above in which one or more hydrogen atoms are replaced with one or more halogen atoms that may be the same or different. Examples of C₁-C₆-haloalkoxy include but are not limited to chloromethoxy, bromomethoxy, dichloro-methoxy, trichloromethoxy, fluoromethoxy, difluoromethoxy, trifluoromethoxy, chlorofluoromethoxy, dichlorofluoromethoxy, chlorodifluoromethoxy, 1-chloroethoxy, 1-bromoethoxy, 1-fluoroethoxy, 2-fluoroethoxy, 2,2-difluoroethoxy, 2,2,2-trifluoroethoxy, 2-chloro-2-fluoroethoxy, 2-chloro-2,2-difluoroethoxy, 2,2-dichloro-2-fluoroethoxy, 2,2,2-trichloroethoxy, pentafluoroethoxy and 1,1,1-trifluoroprop-2-oxy.

The term “C₁-C₆-haloalkoxy” as used herein refers to a C₁-C₆-alkoxy group as defined above in which one or more hydrogen atoms are replaced with one or more halogen atoms that may be the same or different.

The term “C₁-C₆-hydroxyalkyl” as used herein refers to a C₁-C₆-alkyl group as defined above in which at least one hydrogen atom is replaced with a hydroxyl group. Examples of C₁-C₆-hydroxyalkyl include but are not limited to hydroxymethyl, 1-hydroxyethyl, 2-hydroxyethyl, 1,2-dihydroxyethyl, 3-hydroxypropyl, 2-hydroxypropyl, 1-hydroxypropyl, 1-hydroxypropan-2-yl, 2-hydroxypropan-2-yl, 2, 3-dihydroxypropyl and 1,3-dihydroxypropan-2-yl.

The term “C₁-C₆-alkylsulfanyl” as used herein refers to a saturated, linear or branched group of formula (C₁-C₆-alkyl)-S—, in which the term “C₁-C₆-alkyl” is as defined herein. Examples of C₁-C₆-alkylsulfanyl include but are not limited to methylsulfanyl, ethylsulfanyl, propylsulfanyl, isopropylsulfanyl, butylsulfanyl, sec-butylsulfanyl, isobutylsulfanyl, tert-butylsulfanyl, pentylsulfanyl, isopentylsulfanyl, hexylsulfanyl group.

The term “C₁-C₆-haloalkylsulfanyl” as used herein refers to a C₁-C₆-alkylsulfanyl as defined above in which one or more hydrogen atoms are replaced with one or more halogen atoms that may be the same or different.

The term “C₁-C₆-alkylsulfinyl” s used herein refers to a saturated, linear or branched group of formula (C₁-C₆-alkyl)-S(═O)—, in which the term “C₁-C₆-alkyl” is as defined herein. Examples of C₁-C₆-alkylsulfinyl include but are not limited to saturated, straight-chain or branched alkylsulfinyl radicals having 1 to 8, preferably 1 to 6 and more preferably 1 to 4 carbon atoms, for example (but not limited to) C₁-C₆-alkylsulfinyl such as methylsulfinyl, ethylsulfinyl, propylsulfinyl, 1-methylethylsulfinyl, butylsulfinyl, 1-methylpropylsulfinyl, 2-methylpropylsulfinyl, 1,1-dimethylethylsulfinyl, pentylsulfinyl, 1-methylbutylsulfinyl, 2-methylbutylsulfinyl, 3-methylbutylsulfinyl, 2,2-dimethylpropylsulfinyl, 1-ethylpropyl-sulfinyl, 1,1-dimethylpropylsulfinyl, 1,2-dimethylpropylsulfinyl, hexylsulfinyl, 1-methylpentylsulfinyl, 2-methylpentylsulfinyl, 3-methylpentylsulfinyl, 4-methylpentylsulfinyl, 1,1-dimethylbutylsulfinyl, 1,2-dimethylbutylsulfinyl, 1,3-dimethylbutylsulfinyl, 2,2-dimethylbutylsulfinyl, 2,3-dimethylbutylsulfinyl, 3,3-dimethylbutylsulfinyl, 1-ethylbutylsulfinyl, 2-ethylbutylsulfinyl, 1,1,2-trimethylpropylsulfinyl, 1,2,2-trimethylpropylsulfinyl, 1-ethyl-1-methylpropylsulfinyl and 1-ethyl-2-methylpropylsulfinyl.

The term “C₁-C₆-haloalkylsulfinyl” as used herein refers to a C₁-C₆-alkylsulfinyl as defined above in which one or more hydrogen atoms are replaced with one or more halogen atoms that may be the same or different.

The term “C₁-C₆-alkylsulfonyl” s used herein refers to a saturated, linear or branched group of formula (C₁-C₆-alkyl)-S(═O)₂—, in which the term “C₁-C₆-alkyl” is as defined herein. Examples of C₁-C₆-alkylsulfonyl include but are not limited to methylsulfonyl, ethylsulfonyl, propylsulfonyl, 1-methylethylsulfonyl, butylsulfonyl, 1-methylpropylsulfonyl, 2-methylpropylsulfonyl, 1,1-dimethylethylsulfonyl, pentylsulfonyl, 1-methylbutylsulfonyl, 2-methylbutylsulfonyl, 3-methylbutylsulfonyl, 2,2-dimethylpropylsulfonyl, 1-ethylpropylsulfonyl, 1,1-dimethylpropylsulfonyl, 1,2-dimethylpropylsulfonyl, hexylsulfonyl, 1-methylpentylsulfonyl, 2-methylpentylsulfonyl, 3-methylpentylsulfonyl, 4-methylpentylsulfonyl, 1,1-dimethylbutylsulfonyl, 1,2-dimethylbutylsulfonyl, 1,3-dimethylbutylsulfonyl, 2,2-dimethylbutylsulfonyl, 2,3-dimethylbutylsulfonyl, 3,3-dimethylbutylsulfonyl, 1-ethylbutylsulfonyl, 2-ethylbutylsulfonyl, 1,1,2-trimethylpropylsulfonyl, 1,2,2-trimethylpropylsulfonyl, 1-ethyl-1-methylpropylsulfonyl and 1-ethyl-2-methylpropylsulfonyl.

The term “C₁-C₆-haloalkylsulfonyl” as used herein refers to a C₁-C₆-alkylsulfonyl as defined above in which one or more hydrogen atoms are replaced with one or more halogen atoms that may be the same or different.

The term “C₁-C₆-alkylcarbonyl” as used herein refers to a saturated, linear or branched group of formula (C₁-C₆-alkyl)-C(═O)—, in which the term “C₁-C₆-alkyl” is as defined herein.

The term “C₁-C₆-haloalkylcarbonyl” as used herein refers to a C₁-C₆-alkylcarbonyl as defined above in which one or more hydrogen atoms are replaced with one or more halogen atoms that may be the same or different.

The term “C₁-C₆-alkoxycarbonyl” as used herein refers to a saturated, linear or branched group of formula (C₁-C₆-alkoxy)-C(═O)—, in which the term “C₁-C₆-alkoxy” is as defined herein.

The term “C₁-C₆-haloalkoxycarbonyl” as used herein refers to a C₁-C₆-alkoxycarbonyl as defined above in which one or more hydrogen atoms are replaced with one or more halogen atoms that may be the same or different.

The term “C₁-C₆-dialkylamino” as used herein refers to an amino radical having two independently selected C₁-C₆-alkyl groups as defined herein. Examples of C₁-C₆-dialkylamino include but are not limited to N,N-dimethylamino, N,N-diethylamino, N,N-diisopropylamino, N-ethyl-N-methylamino, N-methyl-N-n-propylamino, N-isopropyl-N-n-propylamino and N-tert-butyl-N-methylamino.

The term “non-aromatic C₃-C₁₂-carbocycle” as used herein refers to a non-aromatic, saturated or unsaturated, hydrocarbon ring system in which all of the ring members, which vary from 3 to 12, are carbon atoms. The ring system may be monocyclic or polycyclic (fused, spiro or bridged). Non-aromatic C₃-C₁₂-carbocycles include but are not limited to C₃-C₁₂-cycloalkyl (mono or bicyclic), C₃-C₁₂-cycloalkenyl (mono or bicyclic), bicylic system comprising an aryl (e.g. phenyl) fused to a monocyclic C₃-C₈-cycloalkyl (e.g. tetrahydronaphthalenyl, indanyl), bicylic system comprising an aryl (e.g. phenyl) fused to a monocyclic C₃-C₈-cycloalkenyl (e.g. indenyl, dihydronaphthalenyl) and tricyclic system comprising a cyclopropyl connected through one carbon atom to a bicylic system comprising an aryl (e.g. phenyl) fused to a monocyclic C₃-C₈-cycloalkyl or to a monocyclic C₃-C₈-cycloalkenyl. The non-aromatic C₃-C₁₂-carbocycle can be attached to the parent molecular moiety through any carbon atom.

The term “C₃-C₁₂-cycloalkyl” as used herein refers to a saturated, monovalent, mono- or bicylic hydrocarbon ring which contains 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12 carbon atoms. Examples of monocyclic C₃-C₈-cycloalkyls include but are not limited to cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, or cyclooctyl. Examples of bicyclic C₆-C₁₂-cycloalkyls include but are not limited to bicyclo[3.1.1]heptane, bicyclo[2.2.1]heptane, bicyclo[2.2.2]octane, bicyclo[3.2.2]nonane, bicyclo[3.3.1]nonane, bicyclo[4.2.0]octyl, octahydropentalenyl and bicyclo[4.2.1]nonane.

The term “C₃-C₁₂-cycloalkylene” as used herein refers to a divalent C₃-C₁₂-cycloalkyl group as defined herein, such as cyclopropylene, cyclobutylene, cyclopentylene, cyclohexylene, cycloheptylene and bicyclo[2.2.1]hept-2-ylene.

The term “C₃-C₁₂-cycloalkenyl” as used herein refers to an unsaturated, monovalent, mono- or bicylic hydrocarbon ring which contains 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12 carbon atoms. Examples of monocyclic C₃-C₈-cycloalkenyl group include but are not limited to cyclobutenyl, cyclopentenyl, cyclohexenyl, cycloheptenyl and cyclooctenyl group. Examples of bicyclic C₆-C₁₂-cycloalkenyl group include but are not limited to bicyclo[2.2.1]hept-2-enyl or bicyclo[2.2.2]oct-2-enyl.

The term “C₃-C₁₂-cycloalkenylene” as used herein refers to a divalent C₃-C₁₂-cycloalkenyl as disclosed herein.

The term “aromatic C₆-C₁₄-carbocycle” or “aryl” as used herein refers to an aromatic hydrocarbon ring system in which all of the ring members, which vary from 6 to 14, preferably from 6 to 10, are carbon atoms. The ring system may be monocyclic or fused polycyclic (e.g. bicyclic or tricyclic). Examples of aryl include but are not limited to phenyl, azulenyl and naphthyl. The aryl can be attached to the parent molecular moiety through any carbon atom. It is further understood that when said aryl group is substituted with one or more substituents, said substituent(s) may be at any positions on said aryl ring(s). Particularly, in the case of aryl being a phenyl group, said substituent(s) may occupy one or both ortho positions, one or both meta positions, or the para position, or any combination of these positions.

The term “non-aromatic 3- to 14-membered heterocycle” as used herein refers to a saturated or unsaturated non-aromatic ring system comprising 1 to 4 heteroatoms independently selected from the group consisting of oxygen, nitrogen and sulfur. If the ring system contains more than one oxygen atoms, they are not directly adjacent. Non aromatic heterocycles include but are not limited to 3- to 7-membered monocyclic non-aromatic heterocycles and 6- to 14-membered polycyclic (e.g. bicyclic or tricyclic) non-aromatic heterocycles. The non-aromatic 3- to 14-membered heterocycle can be connected to the parent molecular moiety through any carbon atom or nitrogen atom contained within the heterocycle.

The term “non-aromatic 3- to 7-membered monocyclic heterocycle” as used herein refers to a 3-, 4-, 5-, 6- or 7-membered monocyclic ring system containing 1, 2 or 3 heteroatoms independently selected from the group consisting of oxygen, nitrogen and sulfur where the ring system is saturated or unsaturated but not aromatic. For instance, the heterocycle may comprise one to three nitrogen atoms, or one or two oxygen atoms, or one or two sulfur atoms, or one to three nitrogen atoms and one oxygen atom, or one to three nitrogen atoms and a sulfur atom or one sulfur atom and one oxygen atom. Examples of saturated non-aromatic heterocycles include but are not limited to 3-membered ring such as oxiranyl, aziridinyl, 4-membered ring such as azetidinyl, oxetanyl, thietanyl, 5-membered ring such as tetrahydrofuranyl, 1,3-dioxolanyl, tetrahydrothienyl, pyrrolidinyl, pyrazolidinyl, imidazolidinyl, triazolidinyl, isoxazolidinyl, oxazolidinyl, oxadiazolidinyl, thiazolidinyl, isothiazolidinyl, thiadiazolidinyl, 6-membered ring such as piperidinyl, hexahydropyridazinyl, hexahydropyrimidinyl, piperazinyl, triazinanyl, hexahydrotriazinyl, tetrahydropyranyl, dioxanyl, tetrahydrothiopyranyl, dithianyl, morpholinyl, 1,2-oxazinanyl, oxathianyl, thiomorpholinyl or 7-membered ring such as oxepanyl, azepanyl, 1,4-diazepanyl and 1,4-oxazepanyl. Examples of unsaturated non-aromatic hererocyles include but are not limited to 5-membered ring such as dihydrofuranyl, 1,3-dioxolyl, dihydrothienyl, pyrrolinyl, dihydroimidazolyl, dihydropyrazolyl, isoxazolinyl, dihydrooxazolyl, dihydrothiazolyl or 6-membered ring such as pyranyl, thiopyranyl, thiazinyl and thiadiazinyl.

The term “non-aromatic 6- to 14-membered polycyclic heterocycle” as used herein refers to a 6-, 7-, 8-, 9-, 10-, 11-, 12-, 13- or 14-membered polycyclic (e.g. bicyclic or tricyclic) ring system containing 1, 2 or 3 heteroatoms independently selected from the group consisting of oxygen, nitrogen and sulfur where the ring system is saturated or unsaturated but not aromatic. Non-aromatic bicyclic heterocycles may consist of a monocyclic heteroaryl as defined herein fused to a monocyclic C₃-C₈-cycloalkyl, a monocyclic C₃-C₈-cycloalkenyl or a monocyclic non-aromatic heterocycle or may consist of a monocyclic non-aromatic heterocycle fused either to an aryl (e.g. phenyl), a monocyclic C₃-C₈-cycloalkyl, a monocyclic C₃-C₈-cycloalkenyl or a monocyclic non-aromatic heterocycle. When two monocyclic heterocycles (aromatic or non-aromatic) comprising nitrogen atoms are fused, nitrogen atom may be at the bridgehead (e.g. 4,5,6,7-tetrahydropyrazolo[1,5-a]pyridinyl, 5,6,7,8-tetrahydro-[1,2,4]triazolo[1,5-a]pyridinyl, 5,6,7,8-tetrahydroimidazo[1,2-a]pyridinyl). Non-aromatic tricyclic heterocycles may consist of a monocyclic cycloalkyl connected through one common atom to a non-aromatic bicyclic heterocycle.

The term “non-aromatic 3- to 7-membered monocyclic heterocyclylene” as used herein refers to a divalent non-aromatic 3- to 7-membered monocyclic heterocycle as disclosed herein.

The term “aromatic 5- to 14-membered heterocycle” or “heteroaryl” as used herein refers to an aromatic ring system comprising 1 to 4 heteroatoms independently selected from the group consisting of oxygen, nitrogen and sulfur. If the ring system contains more than one oxygen atom, they are not directly adjacent. Aromatic heterocycles include aromatic 5- or 6-membered monocyclic heterocycles and 6- to 14-membered polycyclic (e.g. bicyclic or tricyclic) aromatic heterocycles. The 5- to 14-membered aromatic heterocycle can be connected to the parent molecular moiety through any carbon atom or nitrogen atom contained within the heterocycle.

The term “aromatic 5- or 6-membered monocyclic heterocycle” or “monocyclic heteroaryl” as used herein refers to a 5- or 6-membered monocyclic ring system containing 1, 2, 3 or 4 heteroatoms independently selected from the group consisting of oxygen, nitrogen and sulfur. Examples of 5-membered monocyclic heteroaryl include but are not limited to furyl (furanyl), thienyl, pyrrolyl, pyrazolyl, imidazolyl, triazolyl, tetrazolyl, isoxazolyl, oxazolyl, oxadiazolyl, oxatriazolyl, isothiazolyl, thiazolyl, thiadiazolyl and thiatriazolyl. Examples of 6-membered monocyclic heteroaryl include but are not limited to pyridinyl, pyridazinyl, pyrimidinyl, pyrazinyl, triazinyl, tetrazinyl.

The term “6- to 14-membered polycyclic aromatic heterocycle” or “polycyclic heteroaryl” as used herein refers to a 6-, 7-, 8-, 9-, 10-, 11-, 12-, 13- or 14-membered polycyclic (e.g. bicyclic or tricyclic) ring system containing 1, 2 or 3 heteroatoms independently selected from the group consisting of oxygen, nitrogen and sulfur. Aromatic bicyclic heterocycles may consist of a monocyclic heteroaryl as defined herein fused to an aryl (e.g. phenyl) or to a monocyclic heteroaryl. Examples of bicyclic aromatic heterocycle include but are not limited to 9-membered ring such as indolyl, indolizinyl, isoindolyl, benzimadozolyl, imidazopyridinyl, indazolyl, benzotriazolyl, purinyl, benzofuranyl, benzothiophenyl, benzothiazolyl, benzoxazolyl and benzisoxazolyl or 10-membered ring such as quinolinyl, isoquinolinyl, cinnolinyl, quinazolinyl, quinoxalinyl, phthalazinyl, naphthyridinyl, pteridinal and benzodioxinyl. In 9- or 10-membered aromatic bicyclic heterocycles comprising two fused 5- or 6-membered monocyclic aromatic heterocycles, nitrogen atom may be at the bridgehead (e.g. imidazo[1,2-a]pyridinyl, [1,2,4]triazolo[4,3-a]pyridinyl, imidazo[1,2-a]pyridinyl, imidazo[2,1-b]oxazolyl, furo[2,3-d]isoxazolyl). Examples of tricyclic aromatic heterocyle include but are not limited to carbazolyl, acridinyl and phenazinyl.

The terms “non-aromatic C₃-C₁₂-carbocyclyloxy”, “C₃-C₈-cycloalkyloxy”, “aromatic C₆-C₁₄-carbocyclyloxy”, “aromatic 5- to 14-membered heterocyclyloxy”, “non-aromatic 5- to 14-membered heterocyclyloxy” as used herein designate a group of formula —O—R wherein R is respectively a non-aromatic C₃-C₁₂-carbocyclyl, a C₃-C₈-cycloalkyl, an aromatic C₆-C₁₄-carbocyclyl, an aromatic 5- to 14-membered heterocyclyl or a non-aromatic 5- to 14-membered heterocyclyl group as defined herein.

As used herein, when a group is said to be “substituted”, the group may be substituted with one or more substituents. The expression “one or more substituents” refers to a number of substituents that ranges from one to the maximum number of substituents possible based on the number of available bonding sites, provided that the conditions of stability and chemical feasibility are met.

The term “leaving group” as used herein is to be understood as meaning a group which is displaced from a compound in a substitution or an elimination reaction, for example a halogen atom, a trifluoromethanesulphonate (“triflate”) group, alkoxy, methanesulphonate, p-toluenesulphonate, etc.

The terms “as described herein” when referring to a variable A, Q, L, m, T, R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸ incorporates by reference the broad definition of the variable as well as preferred, more preferred and even more preferred definitions, if any.

Not encompassed herein are compounds resulting from combinations which are against natural laws and which the person skilled in the art would therefore exclude based on his/her expert knowledge. For instance, ring structures having three or more adjacent oxygen atoms are excluded.

The compounds of formula (I) can suitably be in their free form, salt form, N-oxide form or solvate form (e.g. hydrate).

Depending on the nature of the substituents, the compound of formula (I) may be present in the form of different stereoisomers. These stereoisomers are, for example, enantiomers, diastereomers, atropisomers or geometric isomers. Accordingly, the invention encompasses both pure stereoisomers and any mixture of these isomers. Where a compound can be present in two or more tautomer forms in equilibrium, reference to the compound by means of one tautomeric description is to be considered to include all tautomer forms.

Any of the compounds of the present invention can also exist in one or more geometric isomer forms depending on the number of double bonds in the compound. Geometric isomers by nature of substituents about a double bond or a ring may be present in cis (═Z—) or trans (=E-) form. The invention thus relates equally to all geometric isomers and to all possible mixtures, in all proportions.

Depending on the nature of the substituents, the compound of formula (I) may be present in the form of the free compound and/or a salt thereof, such as an agrochemically active salt.

Agrochemically active salts include acid addition salts of inorganic and organic acids well as salts of customary bases. Examples of inorganic acids are hydrohalic acids, such as hydrogen fluoride, hydrogen chloride, hydrogen bromide and hydrogen iodide, sulfuric acid, phosphoric acid and nitric acid, and acidic salts, such as sodium bisulfate and potassium bisulfate. Useful organic acids include, for example, formic acid, carbonic acid and alkanoic acids such as acetic acid, trifluoroacetic acid, trichloroacetic acid and propionic acid, and also glycolic acid, thiocyanic acid, lactic acid, succinic acid, citric acid, benzoic acid, cinnamic acid, oxalic acid, saturated or mono- or diunsaturated fatty acids having 6 to 20 carbon atoms, alkylsulphuric monoesters, alkylsulphonic acids (sulphonic acids having straight-chain or branched alkyl radicals having 1 to 20 carbon atoms), arylsulphonic acids or aryldisulphonic acids (aromatic radicals, such as phenyl and naphthyl, which bear one or two sulphonic acid groups), alkylphosphonic acids (phosphonic acids having straight-chain or branched alkyl radicals having 1 to 20 carbon atoms), arylphosphonic acids or aryldiphosphonic acids (aromatic radicals, such as phenyl and naphthyl, which bear one or two phosphonic acid radicals), where the alkyl and aryl radicals may bear further substituents, for example p-toluenesulphonic acid, salicylic acid, p-aminosalicylic acid, 2-phenoxybenzoic acid, 2-acetoxybenzoic acid, etc.

Solvates of the compounds of the invention or their salts are stoichiometric compositions of the compounds with solvents.

The compounds of the invention may exist in multiple crystalline and/or amorphous forms. Crystalline forms include unsolvated crystalline forms, solvates and hydrates.

Aliphatic R¹ and R² substituents as used herein in the expression “aliphatic R¹, R², R³, R⁴ and R⁵ substituents may be substituted with one or more substituents” designates C₁-C₆-alkyl.

Aliphatic R³ and R⁴ substituents as used herein in the expression “aliphatic R¹, R², R³, R⁴ and R⁵ substituents may be substituted with one or more substituents” designates C₁-C₆-alkyl, C₁-C₆-alkoxy, C₁-C₆-alkoxycarbonyl and the C₁-C₆-alkyl moiety of —Si(C₁-C₆-alkyl)₃.

Aliphatic R⁵ substituents as used herein in the expression “aliphatic R¹, R², R³, R⁴ and R⁵ substituents may be substituted with one or more substituents” designates C₁-C₆-alkyl, C₁-C₆-alkoxy, C₁-C₆-alkylsulfanyl, C₁-C₆-alkylsulfinyl, C₁-C₆-alkylsulfonyl and the C₁-C₆-alkyl moiety of —O—Si(C₁-C₆-alkyl)₃.

Aliphatic L substituents as used herein in the expression “aliphatic L substituents may be substituted with one or more L^(Sa) substituents” designates C₁-C₆-alkylene, C₂-C₆-alkenylene, C₂-C₆-alkynylene and the C₁-C₆-alkylene moiety of C₁-C₆-alkylene-C₃-C₈-cycloalkylene, C₃-C₈-cycloalkylene-C₁-C₆-alkylene, C₁-C₆-alkylene-C₃-C₈-cycloalkylene-C₁-C₆-alkylene, C₁-C₆-alkylene-(C═O)—, C₁-C₆-alkylene-C₃-C₈-cycloalkenylene, C₃-C₈-cycloalkenylene-C₁-C₆-alkylene, C₁-C₆-alkylene-C₃-C₈-cycloalkenylene-C₁-C₆-alkylene.

Aliphatic R^(6S) substituents as used herein in the expression “aliphatic R^(6S), R^(c) and R^(d) substituents may be substituted with one or more substituents” designates C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl, C₂-C₆-alkenyloxy, C₂-C₆-haloalkenyloxy, C₁-C₆-alkylsulfanyl, C₁-C₆-haloalkylsulfanyl, C₁-C₆-alkylsulfinyl, C₁-C₆-haloalkylsulfinyl, C₁-C₆-alkylsulfonyl, C₁-C₆-haloalkylsulfonyl and the C₁-C₆-alkyl moiety of —Si(C₁-C₆-alkyl)₃ and —O—Si(C₁-C₆-alkyl)₃.

Aliphatic R^(c) substituents as used herein in the expression “aliphatic R^(6S), R^(c) and R^(d) substituents may be substituted with one or more substituents” designates C₁-C₆-alkyl.

Aliphatic R^(d) substituents as used herein in the expression “aliphatic R^(6S), R^(c) and R^(d) substituents may be substituted with one or more substituents” designates C₁-C₆-alkyl and C₁-C₆-haloalkyl.

Aliphatic R⁷ substituents as used herein in the expression “aliphatic R⁷, R^(e), R^(f) and R⁹ substituents may be substituted with one or more R^(7Sa) substituents” designates C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-hydroxyalkyl, C₁-C₆-alkylcarbonyl, C₁-C₆-haloalkylcarbonyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₁-C₆-alkoxycarbonyl, C₁-C₆-haloalkoxycarbonyl, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl, C₂-C₆-alkenyloxy, C₂-C₆-haloalkenyloxy, C₂-C₆-alkynyloxy, C₂-C₆-haloalkynyloxy, C₁-C₆-alkylsulfanyl, C₁-C₆-haloalkylsulfanyl, C₁-C₆-alkylsulfinyl, C₁-C₆-haloalkylsulfinyl, C₁-C₆-alkylsulfonyl, C₁-C₆-haloalkylsulfonyl and the C₁-C₆-alkyl moiety of —Si(C₁-C₆-alkyl)₃ and —O—Si(C₁-C₆-alkyl)₃.

Aliphatic R^(e) substituents as used herein in the expression “aliphatic R⁷, R^(e), R^(f) and R^(g) substituents may be substituted with one or more R^(7Sa) substituents” designates C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl and C₂-C₆-haloalkynyl.

Aliphatic R^(f) substituents as used herein in the expression “aliphatic R⁷, R^(e), R^(f) and R^(g) substituents may be substituted with one or more R^(7Sa) substituents” designates C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy and the C₁-C₆-alkyl moiety of C₁-C₆-alkylamino and di(C₁-C₆-alkyl)amino.

Aliphatic R^(g) substituents as used herein in the expression “aliphatic R⁷, R^(e), R^(f) and R^(g) substituents may be substituted with one or more R^(7Sa) substituents” designates C₁-C₆-alkyl and C₁-C₆-haloalkyl.

Aliphatic R⁸ substituents as used herein in the expression “aliphatic R⁸, R^(h) and R^(i) substituents may be substituted with one or more R^(8Sa) substituents” designates C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-hydroxyalkyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl, C₂-C₆-alkenyloxy, C₂-C₆-haloalkenyloxy, C₂-C₆-alkynyloxy, C₂-C₆-haloalkynyloxy, C₁-C₆-alkylsulfanyl, C₁-C₆-haloalkylsulfanyl, C₁-C₆-alkylsulfinyl, C₁-C₆-haloalkylsulfinyl, C₁-C₆-alkylsulfonyl, C₁-C₆-haloalkylsulfonyl and the C₁-C₆-alkyl moiety of —Si(C₁-C₆-alkyl)₃ and —O—Si(C₁-C₆-alkyl)₃.

Aliphatic R^(h) substituents as used herein in the expression “aliphatic R⁸, R^(h) and R^(i) substituents may be substituted with one or more R^(8Sa) substituents” designates C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl and C₂-C₆-haloalkynyl.

Aliphatic R^(i) substituents as used herein in the expression “aliphatic R⁸, R^(h) and R^(i) substituents may be substituted with one or more R^(8Sa) substituents” designates C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl and C₂-C₆-haloalkynyl.

Aliphatic Q^(S) substituents as used herein in the expression “aliphatic Q^(S), R^(j) and R^(k) substituents may be substituted with one or more substituents” designates C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkylcarbonyl, C₁-C₆-haloalkylcarbonyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₁-C₆-alkoxycarbonyl, C₁-C₆-haloalkoxycarbonyl, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl, C₂-C₆-alkenyloxy, C₂-C₆-haloalkenyloxy, C₁-C₆-alkylsulfanyl, C₁-C₆-haloalkylsulfanyl, C₁-C₆-alkylsulfinyl, C₁-C₆-haloalkylsulfinyl, C₁-C₆-alkylsulfonyl, C₁-C₆-haloalkylsulfonyl and the C₁-C₆-alkyl moiety of —Si(C₁-C₆-alkyl)₃ and —O—Si(C₁-C₆-alkyl)₃.

Aliphatic R^(j) substituents as used herein in the expression “aliphatic Q^(S), R^(j) and R^(k) substituents may be substituted with one or more substituents” designates C₁-C₆-alkyl, C₁-C₆-haloalkyl and C₁-C₆-alkoxy.

Aliphatic R^(k) substituents as used herein in the expression “aliphatic Q^(S), R^(j) and R^(k) substituents may be substituted with one or more substituents” designates C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy, C₂-C₆ alkenyl and C₂-C₆-haloalkenyl.

Cyclic R¹, R² and R⁵ substituents as used herein in the expression “cyclic R¹, R², R³, R⁴ and R⁵ substituents may be substituted with one or more substituents” designates C₃-C₈-cycloalkyl.

Cyclic R³ and R⁴ substituents as used herein in the expression “cyclic R¹, R², R³, R⁴ and R⁵ substituents may be substituted with one or more substituents” designates C₃-C₈-cycloalkyl, aromatic C₆-C₁₄-carbocycle, non-aromatic 3- to 14-membered heterocycle and aromatic 5- to 14-membered heterocycle.

Cyclic L substituents as used herein in the expression “cyclic or cyclic moiety of L substituents may be substituted with one or more L^(Sc) substituents” designates C₃-C₈-cycloalkylene, C₃-C₈-cycloalkenylene and non-aromatic 3- to 7-membered monocyclic heterocyclylene.

Cyclic L substituents as used herein in the expression “cyclic or cyclic moiety of L substituents may be substituted with one or more L^(Sc) substituents” designates C₃-C₈-cycloalkylene moiety of C₁-C₆-alkylene-C₃-C₈-cycloalkylene, C₃-C₈-cycloalkylene-C₁-C₆-alkylene, C₁-C₆-alkylene-C₃-C₈-cycloalkylene-C₁-C₆-alkylene and the C₃-C₈-cycloalkenylene moiety of C₁-C₆-alkylene-C₃-C₈-cycloalkenylene, C₃-C₈-cycloalkenylene-C₁-C₆-alkylene and C₁-C₆-alkylene-C₃-C₈-cycloalkenylene-C₁-C₆-alkylene.

Cyclic R⁶ substituents as used herein in the expression “cyclic, or cyclic moiety of, R⁶ substituents may be substituted with one or more R^(6S) substituents” designate non-aromatic C₃-C₁₂-carbocycle, aromatic C₆-C₁₄-carbocycle, non-aromatic 3- to 14-membered heterocycle and aromatic 5- to 14-membered heterocycle.

Cyclic moiety of R⁶ substituents as used herein in the expression “cyclic, or cyclic moiety of, R⁶ substituents may be substituted with one or more R^(6S) substituents” designate the non-aromatic C₃-C₁₂-carbocycle of non-aromatic C₃-C₁₂-carbocyclyloxy, the aromatic C₆-C₁₄-carbocyclyle of aromatic C₆-C₁₄-carbocyclyloxy, the aromatic 5- to 14-membered heterocycle of aromatic 5- to 14-membered heterocyclyloxy, the non-aromatic 5- to 14-membered heterocycle of non-aromatic 5- to 14-membered heterocyclyloxy, the non-aromatic C₃-C₁₂-carbocycle of C₁-C₃-alkoxy substituted by a non-aromatic C₃-C₁₂-carbocycle, the aromatic C₆-C₁₄-carbocycle of C₁-C₃-alkoxy substituted by an aromatic C₆-C₁₄-carbocycle, the non-aromatic 3- to 14-membered heterocycle of C₁-C₃-alkoxy substituted by a non-aromatic 3- to 14-membered heterocycle, the aromatic 5- to 14-membered heterocycle of C₁-C₃-alkoxy substituted by an aromatic 5- to 14-membered heterocycle, the non-aromatic C₃-C₁₂-carbocycle of C₁-C₃-haloalkoxy substituted by a non-aromatic C₃-C₁₂-carbocycle, the aromatic C₆-C₁₄-carbocycle of C₁-C₃-haloalkoxy substituted by an aromatic C₆-C₁₄-carbocycle, the non-aromatic 3- to 14-membered heterocycle of C₁-C₃-haloalkoxy substituted by a non-aromatic 3- to 14-membered heterocycle and the aromatic 5- to 14-membered heterocycle of C₁-C₃-haloalkoxy substituted by an aromatic 5- to 14-membered heterocycle.

Cyclic R^(6S) substituents as used herein in the expression “cyclic R^(6S) and R^(c) substituents may be substituted with one or more substituents” designates C₃-C₈-cycloalkyl, C₃-C₈-cycloalkenyl, aromatic C₆-C₁₄-carbocycle, aromatic 5- or 6-membered monocyclic heterocycle and non-aromatic 3- to 7-membered monocyclic heterocycle.

Cyclic moiety of R^(6S) substituents as used herein in the expression “cyclic or cyclic moiety of R^(6S) and cyclic R^(c) substituents may be substituted with one or more substituents” designates the C₃-C₈-cycloalkyl of C₃-C₈-cycloalkyloxy.

Cyclic R^(c) substituents as used herein in the expression “cyclic or cyclic moiety of R^(6S) and cyclic R^(c) substituents may be substituted with one or more substituents” designates C₃-C₈-cycloalkyl.

Cyclic R⁷ substituents as used herein in the expression “cyclic R⁷, R^(e) and R^(g) substituents may be substituted with one or more R^(7Sc) substituents” designates C₃-C₈-cycloalkyl, C₃-C₆-cycloalkenyl, aromatic C₆-C₁₄-carbocycle, aromatic 5- or 6-membered monocyclic heterocycle and non-aromatic 3- to 7-membered monocyclic heterocycle.

Cyclic moiety of R⁷ substituents as used herein in the expression “cyclic or cyclic moiety of R⁷, cyclic R^(e) and cyclic R^(g) substituents may be substituted with one or more R^(7Sc) substituents” designates the C₃-C₈-cycloalkyl of C₃-C₈-cycloalkyloxy, the aromatic C₆-C₁₄-carbocycle of aromatic C₆-C₁₄-carbocyclyloxy, the aromatic 5- or 6-membered monocyclic heterocycle of aromatic 5- or 6-membered monocyclic heterocyclyloxy and the non-aromatic 3- to 7-membered monocyclic heterocycle of non-aromatic 3- to 7-membered monocyclic heterocyclyloxy.

Cyclic R^(e) substituents as used herein in the expression “cyclic R⁷, R^(e) and R^(g) substituents may be substituted with one or more R^(7Sc) substituents” designates C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, aromatic C₆-C₁₄-carbocycle, aromatic 5- or 6-membered monocyclic heterocycle and non-aromatic 3- to 7-membered monocyclic heterocycle.

Cyclic R^(g) substituents” as used herein in the expression “cyclic R⁷, R^(e) and R^(g) substituents may be substituted with one or more R^(7Sc) substituents” designates C₃-C₈-cycloalkyl.

Cyclic R⁸ substituents as used herein in the expression “wherein cyclic R⁸, R^(h) and R^(i) substituents may be substituted with one or more R^(8Sc) substituents” designates C₃-C₈-cycloalkyl, C₃-C₆-cycloalkenyl, aromatic C₆-C₁₄-carbocycle, non-aromatic 3- to 14-membered heterocycle and aromatic 5- to 14-membered heterocycle.

Cyclic moiety of R⁸ substituents as used herein in the expression “wherein cyclic or cyclic moiety of R⁸, cyclic R^(h) and cyclic R^(i) substituents may be substituted with one or more R^(8Sc) substituents” designates the C₃-C₈-cycloalkyl of C₃-C₈-cycloalkyloxy, the aromatic C₆-C₁₄-carbocycle of aromatic C₆-C₁₄-carbocyclyloxy, the non-aromatic 3- to 14-membered heterocycle of non-aromatic 3- to 14-membered heterocyclyloxy and the aromatic 5- to 14-membered heterocycle of aromatic 5- to 14-membered heterocyclyloxy.

Cyclic R^(h) substituents as used herein in the expression “wherein cyclic or cyclic moiety of R⁸, cyclic R^(h) and cyclic R^(i) substituents may be substituted with one or more R^(8Sc) substituents” designates C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, aromatic C₆-C₁₄-carbocycle, aromatic 5- to 14-membered heterocycle and non-aromatic 3- to 7-membered monocyclic heterocycle.

Cyclic R^(i) substituents as used herein in the expression “wherein cyclic R⁸, R^(h) and R^(i) substituents may be substituted with one or more R^(8Sc) substituents” designates C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, aromatic C₆-C₄-carbocycle, aromatic 5- to 14-membered heterocycle and non-aromatic 3- to 7-membered monocyclic heterocycle.

Cyclic Q^(S) substituents as used herein in the expression “cyclic or cyclic moiety of Q^(S) and cyclic R^(k) substituents may be substituted with one or more R^(Qs) substituents” designates C₃-C₈-cycloalkyl, C₃-C₆-cycloalkenyl, non-aromatic 3- to 7-membered monocyclic heterocycle and aromatic 5- to 14-membered heterocycle.

Cyclic moiety of Q^(S) substituents as used herein in the expression “cyclic or cyclic moiety of Q^(S) and cyclic R^(k) substituents may be substituted with one or more R^(Qs) substituents” designates the C₃-C₈-cycloalkyl of C₃-C₈-cycloalkyloxy.

Cyclic R^(k) substituents as used herein in the expression “cyclic Q^(S) and R^(k) substituents may be substituted with one or more R^(Qs) substituents” designates C₃-C₈-cycloalkyl.

Processes for the Preparation of Compounds of Formula (I) and Intermediates

The present invention relates to processes for the preparation of compounds of formula (I) and their intermediates. Unless indicated otherwise, the radicals A, Q, T, L, R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸, m have the meanings given above for the compounds of formula (I). These definitions apply not only to the end products of formula (I) but also to all intermediates.

Compounds of formula (I-a)-(I-f) are various subsets of formula (I). Compounds of formula (I-a-1)-(I-a-7) are various subsets of formula (I-a). All substituents for formula (I-a)-(I-f) and (I-a-1)-(I-a-7) are as defined above for formula (I) unless otherwise noted.

The compounds of formula (I) can be prepared by various routes in analogy to known processes (see e.g. and references therein). Non-limiting examples of suitable processes are herein described.

A compound of formula (I) may be directly obtained by performing process A to I or may be obtained by conversion or derivatization of another compound of formula (I) prepared in accordance with the processes described herein. For instance, a compound of formula (I) can be converted into another compound of formula (I) by replacing one or more substituents of the starting compound of formula (I) by other substituents. Non-limiting examples of such conversion or derivatization are described below (processes J to L).

The processes described herein may be suitably performed using one or more inert organic solvents which is/are customary for the considered reaction. Suitable inert organic solvents can be chosen from the following: aliphatic, alicyclic or aromatic hydrocarbons (e.g. petroleum ether, pentane, hexane, heptane, cyclohexane, methylcyclohexane, ligroin, benzene, toluene, xylene or decalin), halogenated aliphatic, alicyclic or aromatic hydrocarbons (e.g. chlorobenzene, dichlorobenzene, dichloromethane, chloroform, carbon tetrachloride, 1,2-dichloroethane or trichloroethane), ethers (e.g. diethyl ether, diisopropyl ether, methyl t-butyl ether, methyl t-amyl ether, dioxane, tetrahydrofuran, 2-methyltetrahydrofuran, 1,2-dimethoxyethane, 1,2-diethoxyethane or anisole), ketones (e.g. acetone, methyl ethyl ketone, methyl isopropyl ketone and methyl isobutyl ketone), esters (e.g. methyl acetate, ethyl acetate or butyl acetate), alcohols (e.g. methanol, ethanol, propanol, iso-propanol, butanol, tert-butanol), nitriles (e.g. acetonitrile, propionitrile, n- or i-butyronitrile or benzonitrile), amides (e.g. N,N-dimethylformamide, N,N-dimethylacetamide, N-methylformanilide, N-methylpyrrolidone or hexamethylphosphoric triamide), sulfoxides (e.g. dimethyl sulfoxide) or sulfones (e.g. sulfolane), ureas (e.g. 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone) or any mixture thereof.

Some processes described herein may require or be optionally performed using one or more inorganic or organic bases which are customary for such reactions. Examples of suitable inorganic and organic bases include, but are not limited to, alkaline earth metal or alkali metal carbonates (e.g. sodium carbonate, potassium carbonate, potassium bicarbonate, sodium bicarbonate or cesium carbonate), alkali metal hydrides (e.g. sodium hydride), alkaline earth metal or alkali metal hydroxides (e.g. sodium hydroxide, calcium hydroxide, potassium hydroxide or other ammonium hydroxide derivatives), alkaline earth metal, alkali metal or ammonium fluorides (e.g. potassium fluoride, cesium fluoride or tetrabutylammonium fluoride), alkali metal or alkaline earth metal acetates (e.g. sodium acetate, lithium acetate, potassium acetate or calcium acetate), alkali metal alcoholates (e.g. potassium tert-butoxide or sodium tert-butoxide), alkali metal phosphates (e.g. tri-potassium phosphate), tertiary amines (e.g. trimethylamine, triethylamine, tributylamine, N,N-dimethylaniline, N,N-dicyclohexylmethylamine, N,N-diisopropylethylamine, N-methylpiperidine, N,N-dimethylaminopyridine, diazabicyclooctane (DABCO), diazabicyclononene (DBN), diazabicycloundecene (DBU), quinuclidine, 3-acetoxyquinuclidine, guanidines or aromatic bases (e.g. pyridines, picolines, lutidines or collidines).

Some of the processes described herein may be optionally performed in the presence of a transition metal catalyst, such as a metal (e.g. copper or palladium) salt or complex, if appropriate in the presence of a ligand.

Suitable copper salts or complexes and their hydrates include, but are not limited to, copper metal, copper(I) iodide, copper(I) chloride, copper(I) bromide, copper(II) chloride, copper(II) bromide, copper(II) oxide, copper(I) oxide, copper(II) acetate, copper(I) acetate, copper(I) thiophene-2-carboxylate, copper(I) cyanide, copper(II) sulfate, copper(II) bis(2,2,6,6-tetramethyl-3,5-heptanedionate), copper(II) trifluoromethanesulfonate, tetrakis(acetonitrile)copper(I) hexafluorophosphate, tetrakis(acetonitrile)-copper(I) tetrafluoroborate.

It is also possible to generate in situ a suitable copper complex in the reaction mixture by separate addition to the reaction of a copper salt and a ligand or salt, such as ethylenediamine, N,N-dimethylethylenediamine, N,N′-dimethylethylenediamine, rac-trans-1,2-diaminocyclohexane, rac-trans-N,N′-dimethylcyclohexane-1,2-diamine, 1,1′-binaphthyl-2,2′-diamine, N,N,N′,N′-tetramethylethylenediamine, proline, N,N-dimethylglycine, quinolin-8-ol, pyridine, 2-aminopyridine, 4-(dimethylamino)pyridine, 2,2′-bipyridyl, 2,6-di(2-pyridyl)pyridine, 2-picolinic acid, 2-(dimethylaminomethyl)-3-hydroxypyridine, 1,10-phenanthroline, 3,4,7,8-tetramethyl-1,10-phenanthroline, 2,9-dimethyl-1,10-phenanthroline, 4,7-dimethoxy-1,10-phenanthroline, N,N′-bis[(E)-pyridin-2-ylmethylidene]cyclohexane-1,2-diamine, N-[(E)-phenylmethylidene], N-[(E)-phenylmethylidene]-cyclohexanamine, 1,1,1-tris(hydroxymethyl)ethane, n-butylimidazol, ethylene glycol, 2,2,6,6-tetramethylheptane-3,5-dione, 2-(2,2-dimethylpropanoyl)cyclohexanone, acetylacetone, dibenzoylmethane, 2-(2-methyl-propanoyl)cyclohexanone, biphenyl-2-yl(di-tert-butyl)phosphane, ethylenebis-(diphenylphosphine), N,N-diethylsalicylamide, 2-hydroxybenzaldehyde oxime, oxo[(2,4,6-trimethylphenyl)amino]acetic acid or 1H-pyrrole-2-carboxylic acid.

Suitable palladium salts or complexes include, but are not limited to, palladium chloride, palladium acetate, tetrakis(triphenylphosphine)palladium(0), bis(dibenzylideneacetone)palladium(0), tris(dibenzylidene-acetone)dipalladium(0), bis(triphenylphosphine)palladium(II) dichloride, [1,1′-bis(diphenyl-phosphino)ferrocene]dichloropalladium(II), bis(cinnamyl)dichlorodipalladium(II), bis(allyl)-dichlorodipalladium(II) or [1,1′-Bis(di-tert-butylphosphino)ferrocene]dichloropalladium(II).

It is also possible to generate a palladium complex in the reaction mixture by separate addition to the reaction of a palladium salt and a ligand or salt, such as triethylphosphine, tri-tert-butylphosphine, tri-tert-butylphosphonium tetrafluoroborate, tricyclohexylphosphine, 2-(dicyclohexylphosphino)biphenyl, 2-(di-tert-butylphosphino)biphenyl, 2-(dicyclohexylphosphino)-2′-(N,N-dimethylamino)biphenyl, 2-(tert-butylphosphino)-2′-(N,N-dimethylamino)biphenyl, 2-di-tert-butylphosphino-2′,4′,6′-triisopropylbiphenyl, 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl, 2-dicyclohexylphosphino-2,6′-dimethoxybiphenyl, 2-dicyclohexylphosphino-2′,6′-diisopropoxybiphenyl, triphenyl-phosphine, tris-(o-tolyl)phosphine, sodium 3-(diphenylphosphino)benzenesulfonate, tris-(2-methoxy-phenyl)phosphine, 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl, 1,4-bis(diphenylphosphino)butane, 1,2-bis(diphenylphosphino) ethane, 1,4-bis(dicyclohexylphosphino)butane, 1,2-bis(dicyclohexylphosphino)-ethane, 2-(dicyclohexylphosphino)-2′-(N,N-dimethylamino)-biphenyl, 1,1′-bis(diphenylphosphino)-ferrocene, (R)-(−)-1-[(S)-2-diphenylphosphino)ferrocenyl]ethyldicyclohexylphosphine, tris-(2,4-tert-butyl-phenyl)phosphite, di(1-adamantyl)-2-morpholinophenylphosphine or 1,3-bis(2,4,6-trimethylphenyl)imidazolium chloride.

The appropriate catalyst and/or ligand may be chosen from commercial catalogues such as “Metal Catalysts for Organic Synthesis” by Strem Chemicals or from reviews (Chemical Society Reviews (2014), 43, 3525, Coordination Chemistry Reviews (2004), 248, 2337 and references therein).

Some of the processes described herein may be performed by metallo-photoredox catalysis according to methods reported in the literature (Nature chemistry review, (2017) 0052 and references therein; Science (2016) 352, 6291, 1304; Org. Lett. 2016, 18, 4012, J. Org. Chem 2016, 81, 6898; J. Am. Chem. Soc. 2016, 138, 12715, J. Am. Chem. Soc. 2016, 138, 13862; J. Am. Chem. Soc. 2016, 138, 8034; J. Org. Chem. 2016, 81, 12525, J. Org. Chem. 2015, 80, 7642). The process is then performed in the presence a photosensitizer, such as Ir and Ru complexes or organic dyes, and a metal catalyst such as Ni complexes. The reaction can be performed in the presence of a ligand and if appropriate in the presence of a base under irradiation with blue or white light.

Suitable photosensitizers include, but are not limited to, Ir(III) photocatalyst such as [Ir(dFCF₃ppy)₂(bpy)]PF₆ (dFCF₃ppy=2-(2,4-difluorophenyl)-5-trifluoromethylpyridine, bpy=2,2′-bipyridine), [Ir(dFCF₃ppy)₂(dtbbpy)]PF₆ (dtbbpy=4,4′-di-tert-butyl-2,2′-bipyridine), Ir(ppy)₂(dtbbpy)PF₆ (ppy=2-phenylpyridine), Ir(ppy)₂(bpy)PF₆, Ir(dFppy)₃PFs (dFCF₃ppy=2-(2,4-difluorophenyl)pyridine), fac-Ir(ppy)₃, (Ir[diF(5-Me)ppy]₂(tetraMePhen)PF₆ (diF(5-Me)ppy=2-(2,4-difluorophenyl)-5-methy-lpyridine, tetraMePhen=3,4,7,8-tetramethyl-1,10-phenanthroline), Ru(II) photocatalyst such as Ru(bpy)₃C₁₂ or Ru(bpy)₃(PF₆)₂ or organic dyes like 9-mesityl-10-acridinium perchlorate or tetrafluoroborate, or 2,4,5,6-tetra-9H-carbazol-9-yl-1,3-benzenedicarbonitrile, 9-fluorenone and 9,10-phenanthrenequinone.

Suitable nickel catalysts include, but are not limited to, bis(1,5-cyclooctadiene)nickel (0), nickel(II) chloride, nickel(II) bromide, nickel(II) iodide under their anhydrous or hydrate forms or as dimethoxyethane complexes, nickel(II) acetylacetonate, nickel(II) nitrate hexahydrate. These nickel catalysts can be used in combination with bipyridine ligand such as 2,2′-bipyridine, 4,4′-di-tert-butyl-2,2′-bipyridine, 4,4′-dimethoxy-2,2′-bipyridine, 4,4′-dimethyl-2,2′-bipyridine or phenantroline such as 1,10-phenanthroline, 4,7-dimethyl-1,10-phenantroline, 4,7-dimethoxy-1,10-phenantroline or diamines such as N,N,N′,N′-tetramethylethylenediamine or dione such as tetramethylheptanedione.

The processes described herein may be performed at temperature ranging from −105° C. to 250° C., preferably from −78° C. to 185° C.

The reaction time varies as a function of the scale of the reaction and of the reaction temperature, but is generally between a few minutes and 48 hours.

The processes described herein are generally performed under standard pressure. However, it is also possible to work under elevated or reduced pressure.

The processes described herein may optionally be performed under microwave irradiation under standard or elevated pressure.

In the processes described herein, the starting materials are generally used in approximately equimolar amounts. However, it is also possible to use one of the starting materials in a relatively large excess.

Processes for the Preparation of Compounds of Formula (I)

Process A

A compound of formula (I-a-1) (i.e. compound of formula (I) wherein A is O, T is hydrogen and m is 1 or 2) can be prepared by a process, as shown in scheme 1, comprising the steps of:

-   -   when W is hydrogen, treating the compound of formula (4) with a         dehydrating agent, optionally in the presence of a base to         obtain directly the compound of formula (I-a-1);     -   when W is an aminoprotecting group, treating the compound of         formula (4) with a dehydrating agent, optionally in the presence         of a base, and then performing a deprotection step to obtain the         compound of formula (I-a-1).

The compound of formula (I-a-1) can be obtained by treating a compound of formula (4) with a dehydrating agent such as POCl₃, P₂O₅ or triflic anhydride, optionally in the presence of a base. Such methods to form oxadiazine rings are known and have been described in the literature (J. Med. Chem. 2017, 60, 2383-2400). The reaction may be performed in any customary inert organic solvents. Preference is given to using optionally halogenated aliphatic, alicyclic or aromatic hydrocarbons, such as petroleum ether, hexane, heptane, cyclohexane, methylcyclohexane, benzene, toluene, xylene or decalin; chlorobenzene, dichlorobenzene, dichloromethane, chloroform, carbon tetrachloride, dichlorethane or trichlorethane; ethers, such as diisopropyl ether, methyl t-butyl ether, methyl t-amyl ether, dioxane, tetrahydrofuran, 1,2-dimethoxyethane, 1,2-diethoxyethane or anisole; nitriles, such as acetonitrile, propionitrile, n- or i-butyronitrile or benzonitrile; alcohols, such as ethanol or isopropanol.

When W represents an amino protecting group, step 3 is followed by an additional deprotection step using reaction conditions described in the literature (Greene's Protective Groups in organic Synthesis; Peter G. M. Wuts; Wiley; Fifth Edition; 2014; 895-1194). For example a tert-butoxycarbonyl group can be removed in acidic medium such as hydrochloric acid or trifluoroacetic acid.

Compound of formula (4) can be obtained by:

-   -   reacting a compound of formula (1) with an amine of formula (2)         or one of its salt to provide a compound of formula (3);     -   removing the phtalimide group of compound (3) to provide a         compound of formula (4). Reaction conditions to remove a         phtalimide group are well known and have been reported in the         literature (Greene's Protective Groups in organic Synthesis;         Peter G. M. Wuts; Wiley; Fifth Edition; 2014; 1012-1014).

Compounds of formula (1) can be prepared by one or more processes described herein (see processes N, O and P)

Amines of formula (2) can be prepared by process S described herein.

Compounds of formula (1) wherein U¹ is a hydroxyl group can be reacted with an amine of formula (2) in the presence of a condensing reagent by means of methods described in the literature (e.g. Tetrahedron 2005, 61, 10827-10852). Examples of suitable condensing reagents include, but are not limited to, halogenating reagents (e.g. phosgene, phosphorous tribromide, phosphorous trichloride, phosphorous pentachloride, phosphorous trichloride oxide, oxalyl chloride or thionyl chloride), dehydrating reagents (e.g. ethyl chloroformate, methyl chloroformate, isopropyl chloroformate, isobutyl chloroformate or methanesulfonyl chloride), carbodiimides (e.g. N,N′-dicyclohexylcarbodiimide (DCC)) or other customary condensing (or peptide coupling) reagents (e.g. phosphorous pentoxide, polyphosphoric acid, bis(2-oxo-3-oxazolidinyl)phosphinic chloride, 1-[Bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium 3-oxide hexafluorophosphate (HATU), N,N′-carbonyl-diimidazole, 2-ethoxy-N-ethoxycarbonyl-1,2-dihydroquinoline (EEDQ), triphenylphosphine/tetrachloro-methane, 4-(4,6-dimethoxy[1.3.5]-triazin-2-yl)-4-methylmorpholinium chloride hydrate, bromo-tripyrrolidinophosphoniumhexafluorophosphate or propanephosphonic anhydride (T3P).

Compounds of formula (1) wherein U¹ is a halogen atom can be reacted with an amine of formula (2) in the presence of an acid scavenger by means of well-known methods. Suitable acid scavengers include any inorganic and organic bases, as described herein, which are customary for such reactions. Preference is given to alkali metal carbonates, alkaline earth metal acetates, tertiary amines or aromatic bases.

Compounds of formula (1) wherein U¹ is a C₁-C₆-alkoxy group can be reacted with an excess of amine of formula (2), optionally in the presence of a Lewis acid such as trimethylaluminium.

Process B

A compound of formula (I-a-1) (i.e. compound of formula (I) wherein A is O, T is hydrogen and m is 1 or 2) can be prepared by a process comprising the steps of reacting a compound of formula (7) with a compound of formula (8) in the presence of a base (e.g. organic or inorganic base) and optionally in the presence of a suitable copper salt or complex as shown in scheme 2.

Compounds of formula (7) can be prepared by:

-   -   reacting a compound of formula (5) with an amine of formula (2)         or one of its salt to obtain a compound of formula (6a);     -   removing the phtalimide group of compound (6a) to obtain a         compound of formula (6b);     -   when W is hydrogen, treating the compound of formula (6b) with a         dehydrating agent, optionally in the presence of a base to         obtain directly the compound of formula (7);     -   when W is an aminoprotecting group, treating the compound of         formula (6b) with a dehydrating agent, optionally in the         presence of a base and then performing a deprotection step to         obtain the compound of formula (7),         in the same conditions as described herein for process A.

The reaction of compound of formula (7) with a compound of formula (8) may be performed in the presence of a transition metal catalyst such as a copper salt or complex, and if appropriate in the presence of a ligand as described herein.

Compounds of formula (5) are commercially available or may be prepared by process Q described herein.

Compounds of formula (8) are commercially available or may be obtained by conversion or derivatization of another compound of formula (8) in accordance to well-known methods.

Process C

A compound of formula (I-a-1) (i.e. compound of formula (I) wherein A is O, T is hydrogen and m is 1 or 2) can be prepared by a process, as shown in scheme 3, comprising the step of adding a reducing agent to the compound of formula (12) under acidic conditions to provide a compound of formula (I-a-1).

Compound of formula (12) can be cyclized under acidic conditions in the presence of a reducing agent such as sodium cyanoborohydride to provide a compound of formula (I-a-1). Reaction conditions to form oxadiazine rings with this methodology are known and have been described in the literature (Heterocycles 2016, 92, 2166-2200).

Compound of formula (12) can be obtained by reacting a compound of formula (10) with a compound of formula (11) in the presence of a base. Suitable bases can be alkali metal hydrides such as sodium hydride, alkali metal carbonates such as potassium carbonate, alkali metal hydroxides such as potassium hydroxide, or phosphazene bases such as BEMP as described in the literature (Heterocycles 2016, 92, 2166-2200).

Compound of formula (10) can be obtained by reacting a compound of formula (9) with hydroxylamine or one of its salt. Reaction conditions to perform such transformations are known and have been reported in the literature (WO2010138600).

Compounds of formula (9) may be prepared by process R described herein.

Compounds of formula (11) are either commercially available or can be prepared by processes described in the literature (Eur. J. Med. Chem. 2014, 84, 302, Eur. J. Med. Chem. 2015, 100, 18-23, WO2017031325).

Process D

A compound of formula (I-a-1) (i.e. compound of formula (I) wherein A is O, T is hydrogen, L is a direct bond and m is 1 or 2) can be prepared by a process comprising the steps of:

-   -   placing a compound of formula (13) under oxidative condition to         provide compound (14);     -   when R⁶—H (15) is an aromatic C₆-C₁₄-carbocycle, a non-aromatic         C₇-C₁₄-carbocycle, a non-aromatic 7- to 14-membered heterocycle,         or an aromatic 5- to 14-membered heterocycle, treating a         compound of formula (14) with a compound of formula (15) under         acidic conditions to form a compound of formula (I-a-1).     -   when R⁶—H (15) is an alcohol (R^(6′)—O)—H or a thiol         (R^(6′)—S)—H derivative, treating a compound of formula (14)         with an halogenating reagent such as SOCl₂ and a compound of         formula (15) to form compounds of formula (I-a-1) in which R⁶         represents an oxy, an alkoxy, or a thiol group.         as shown in scheme 4.

The compound of formula (14) can be reacted with an aromatic C₆-C₁₄-carbocycle, a non-aromatic C₇-C₁₄-carbocycle, a non-aromatic 7- to 14-membered heterocycle, or an aromatic 5- to 14-membered heterocycle (R⁶—H) under acidic conditions to provide a compound of formula (I-a-1). Reaction conditions to form oxadiazine rings with this methodology are known and have been described in the literature (WO2017031325).

Compounds of formula (14) can be obtained from a compound of formula (13) under oxidative conditions, for example in the presence of osmium trioxide and sodium periodate.

Compounds of formula (13) may be prepared by process R described herein.

Process E

A compound of formula (I-a-1) (i.e. compound of formula (I) wherein A is O, T is hydrogen and m is 1 or 2) can be prepared by a process comprising the steps of:

-   -   reacting a compound of formula (18) with a compound of         formula (19) or one of its salt to provide a compound of formula         (20),     -   when E¹ is hydroxyl, converting the compound of formula (20)         into compound of formula (I-a-1) using Mitsunobu reaction         conditions,     -   when E¹ is halogen, converting the compound of formula (20) into         compound of formula (I-a-1) in the presence of a base,         as shown in scheme 5.

Aminoalcohols of formula (19-a, E¹=hydroxyl) are commercially available or may be producible by methods described in the literature (Molecules, 9 (6), 405-426; 2004; WO2017203474). Compounds of formula (19-b, E¹=halogen) or one of its salts can be obtained from the corresponding aminoalcohol by well-known methods.

When E¹ is hydroxyl, the compound of formula (20) can be converted by Step 4 of the process into a compound of formula (I-a-1) using classical Mitsunobu reaction conditions known by the skilled person of the art (Strategic Applications of Named Reactions in Organic Synthesis; Laszlo Kürti, Barbara Czako; Elsevier; 2005; 294-295 and reference herein).

When E¹ is halogen, the compound of formula (20) can be converted by Step 4 of the process into a compound of formula (I-a-1) in the presence of a base as referred herein.

When W represents an amino protecting group, Step 4 is followed by an additional deprotection step using reaction conditions described in the literature (Greene's Protective Groups in organic Synthesis; Peter G. M. Wuts; Wiley; Fifth Edition; 2014; 895-1194) to provide a compound of formula (I-a-1).

Compound of formula (18) can be treated with a compound of formula (19) or one of its salt in the presence of a base such as triethylamine to form a compound of formula (20).

Compound of formula (18) can be obtained by Step 2 of the process by treating an oxime of formula (17) with a halogenating reagent such as NCS. Reaction conditions to perform such transformations have been reported in the literature (WO2013173672; RSC Advances 2015, 5, 58587-58594).

An oxime of formula (17) can be obtained by Step 1 from an aldehyde of formula (16) in the presence of hydroxylamine or one of its salt, optionally in the presence of a base. Such transformations are known and have been reported in the literature (Tetrahedron 2000, 56, 1057-1064; ChemMedChem 2013, 8, 1210-1223).

Aldehydes of formula (16) can be prepared according to well-known methods for the one skilled in the art; for example either by treating the weinreb amide precursor with DIBAL-H (WO2016045591) or by converting the ester precursor into the primary alcohol followed by oxidation of the alcohol into the corresponding aldehyde (WO199850031). The ester precursors to access such aldehydes can be prepared according to Process N, O, P described herein.

Process F

A compound of formula (I-a-1) (i.e. compound of formula (I) wherein A is O, T is hydrogen and m is 1 or 2) or (I-a-2) (i.e. compound of formula (I) wherein A is NH, T is hydrogen and m is 1 or 2) can be prepared by a process comprising the steps of:

-   -   reacting a compound of formula (1) with an amine of formula (19)         or one of its salt to provide a compound of formula (21) under         similar conditions as described in process A,     -   treating a compound of formula (21) with a dehydrating agent         followed by hydroxylamine or hydrazine to form a compound of         formula (20)     -   when E¹ and E² is hydroxyl, converting the compound of         formula (20) into compound of formula (I-a-1) using Mitsunobu         reaction conditions,     -   when E¹ is halogen and E² is hydroxyl or —NH₂, converting the         compound of formula (20) into compound of formula (I-a-1) to         (I-a-2) in the presence of a base,         as shown in scheme 6.

Step 2 and step 3 of process F can be performed using similar reaction conditions as described in process E.

Aminoalcohols of formula (19-a, E¹=hydroxyl) are commercially available or may be producible by methods described in the literature (Molecules, 9 (6), 405-426; 2004; WO2017203474). Compounds of formula (19-b, E¹=halogen) or one of its salt can be obtained from the corresponding aminoalcohol by well-known methods.

Process G

A compound of formula (I-a-1) (i.e. compound of formula (I) wherein A is O, T is hydrogen and m is 1 or 2) or (I-a-2) (i.e. compound of formula (I) wherein A is NH, T is hydrogen and m is 1 or 2) can be prepared by a process comprising the steps of:

-   -   reacting a compound of formula (5) with an amine of formula (19)         to provide a compound of formula (22) under similar conditions         as described in process A,     -   treating a compound of formula (22) with a dehydrating agent         followed by hydroxylamine or hydrazine to form a compound of         formula (23)     -   when E¹ and E² is hydroxyl, converting the compound of         formula (23) into compound of formula (7) using Mitsunobu         reaction conditions,     -   when E¹ is halogen and E² is hydroxyl or —NH₂, converting the         compound of formula (23) into compound of formula (7) or (24) in         the presence of a base,     -   reacting a compound of formula (7) or (24) with a compound of         formula (8) in the presence of a base (e.g. organic or inorganic         base) and optionally in the presence of a suitable copper salt         or complex to provide a compound of formula (I-a-1) or (I-a-2)         as shown in scheme 7.

Process H

A compound of formula (I-a-1) (i.e. compound of formula (I) wherein A is O, T is hydrogen and m is 1 or 2), (I-a-3) (i.e. compound of formula (I) wherein A is CR¹R², T is hydrogen and m is 1 or 2), (I-a-4) (i.e. compound of formula (I) wherein A is C(═O), T is hydrogen and m is 1 or 2) or (I-a-5) (i.e. compound of formula (I) wherein A is S(═O)₂, T is hydrogen and m is 1 or 2) can be prepared by a process comprising the steps of:

-   -   treating a compound of formula (9) with an alkoxide to provide         compound of formula (25),     -   reacting the compound of formula (25) with respectively an amine         of formula (26a-1), (26a-2), (26a-3) or (26a-4),         as shown in scheme 8.

Alternatively, a compound of formula (I-a-5) may be prepared by treating a pyridazine 4-carboxamidine compound with a trans-styrylsulfonyl chloride in analogy to methods described in the literature (J. Org. Chem. 1974, 39, 3080)

The compound of formula (25) can be obtained by treating a compound of formula (9) with an alkoxide such as sodium methanolate or sodium ethanolate according to methods described in the literature (Heterocycles, 34, 1992, 929-935).

The compound of formula (25) is treated with a compound of formula (26-a-1), (26-a-2), (26-a-3) or (26-a-4) and cyclized under acidic conditions to form respectively a compound of formula (I-a-1), (I-a-3), (I-a-4) or (I-a-5). Reaction conditions to perform such transformations based on this methodology have been described in the literature (Heterocycles 2016, 92, 2166-2200).

Amines of formula (26-a-1), (26-a-2), (26-a-3) or (26-a-4) are either commercially available, or may be prepared by methods described in the literature (Molecules, 9 (6), 405-426; 2004, WO2017203474; J. Med. Chem 1985, 28, 694-698; J. Med. Chem 2006, 49, 4333-4343) and by Process S of this invention.

Process I

A compound of formula (L-a-6) (i.e. compound of formula (I) wherein A is O, T is hydrogen and m is 2), can be prepared by a process comprising the steps of:

-   -   treating a compound of formula (9) with an hydroxylamine         derivative (27) in the presence of a suitable base as described         herein to provide compound of formula (28),     -   reacting the compound of formula (28) with a reagent of         formula (29) in the presence of a metal catalyst and a suitable         ligand to provide a compound of formula (30)     -   treating a compound of formula (30) with iodine and phenylsilane         to form a compound of formula (I-a-6),         as shown in scheme 9.

Reagents of formula (27) are either commercially available or producible by processes described in the literature (WO2010099279).

Reagents of formula (29) are commercially available or can be prepared by known processes.

Process J

A compound of formula (I-a-7) (i.e. compound of formula (I) wherein A is CR¹R², T is hydrogen and m is 0) can be prepared by a process comprising the step of reacting a compound of formula (1) with a diamine of formula (31) as shown in scheme 10.

Process J can be performed in the presence of a dehydrating agent such as POCl₃.

Diamines of formula (31) are commercially available or can be prepared by methods described in the literature (Eur. J. Med. Chem 1990, 25(1), 35-44; J. Org. Chem 2012, 77(9), 4375-4384; WO2009003867).

Process K

A compound of formula (I-a) can be converted by means of methods described in the literature to the corresponding compounds (I-b) or (I-c) in one or more steps as shown in scheme 11.

In scheme 11, R^(e), R^(f), R^(g) are as disclosed herein and the aliphatic and cyclic substituents R^(7b), R^(7c), R^(e), R^(f), R^(g) may be substituted as disclosed herein.

Non-limiting examples of conversions performed in accordance with scheme 11 are provided below.

A compound of formula (I-a) wherein R^(7a) is a chlorine atom can be converted into a compound of formula (I-b) wherein R^(7b) is a bromine or an iodine atom by means of methods described in the literature (e.g. WO2016185342, WO2007022937).

A compound of formula (I-a) wherein R^(7a) is a halogen atom can be converted into a compound of formula (I-b) wherein R^(7b) is a hydrogen atom in the presence of a palladium catalyst as reported in the literature (Journal of Molecular Catalysis A: Chemical, 2014, 393, 191-209).

A compound of formula (I-a) wherein R^(7a) is a hydrogen atom or a halogen atom can be converted into a compound of formula (I-b) wherein R^(7b) is cyano, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl, C₁-C₆-alkylsulfanyl, C₁-C₆-haloalkylsulfanyl, C₃-C₈-cycloalkyl, C₃-C₆-cycloalkenyl, aromatic C₆-C_(1a)-carbocycle, aromatic 5- or 6-membered monocyclic heterocycle, non-aromatic 3- to 7-membered monocyclic heterocycle, —N(R^(e))₂ or —C(═O)(OR^(g)) by transition metal catalyzed or metallo-photoredox catalyzed processes as described herein.

A compound of formula (I-b) wherein R^(7b) is a C₂-C₆-alkenyl group substituted by a C₁-C₃-alkoxy can be converted into a compound of formula (I-c) wherein R^(7c) is a C₁-C₆-alkylcarbonyl group by means of methods described in the literature (e.g. J. Org. Chem. 1993, 55, 3114).

The compound of formula (I-c) wherein R^(7c) is a C₁-C₆-alkylcarbonyl group can be further converted in a compound of formula (I-c) wherein R^(7c) is —C(═NR^(f))—C₁-C₆-alkyl group by methods described in the literature (e.g. Greene's Protective Groups in organic Synthesis; Peter G. M. Wuts; Wiley; Fifth Edition; 2014; 655, 661, 667).

A compound of formula (I-c) wherein R^(7c) is a C₁-C₆-alkylcarbonyl group can be further converted in a compound of formula (I-c) wherein R^(7c) is C₁-C₆-hydroxyalkyl group by classical functional group interconversion such as reductions of ketones to alcohols in the presence of NaBH₄ in MeOH.

A compound of formula (I-c) wherein R^(7c) is C₁-C₆-hydroxyalkyl group can be further converted into a compound (I-c) wherein R^(7c) is C₁-C₆-fluoroalkyl in the presence of a fluorinating agent. Non-limitative examples of fluorinating agents include sulfur fluorides such as sulfur tetrafluoride, diethylaminosulfurtrifluoride, morpholinosulfur trifluoride, bis(2-methoxyethyl)aminosulfur trifluoride, 2,2-difluoro-1,3-dimethylimidazolidine or 4-tert-butyl-2,6-dimethylphenylsulfur trifluoride.

A compound of formula (I-a) can be prepared by one or more of the processes herein described.

Process L

A compound of formula (I-a) can be converted by means of methods described in the literature to the corresponding compound of formula (I-d) or compound of formula (I-e) in one or more steps as shown in scheme 12.

Non-limiting examples of conversions performed in accordance with scheme 12 are provided below.

A compound of formula (I-a) can be converted into a compound of formula (I-d) wherein R^(8a) is a halogen atom in the presence of a base and an electrophile such as NCS, NBS, NIS, hexachloroethane, bromine or iodine by means of methods described in the literature (e.g. Org. Lett. 2009, 11, 1837). Suitable bases for carrying out the process can be selected from lithium-diisopropylamide, lithium 2,2,6,6-tetramethylpiperidide, n-butyl lithium, methyl lithium, TMPZnCl·LiCl, TMP₂Zn·2MgCl₂·2LiCl (see e.g. Dissertation Albrecht Metzer 2010, University Munich).

A compound of formula (I-a) can be converted into a compound of formula (I-d) wherein R^(8a) is a C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-hydroxyalkyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, C₃-C₆-cycloalkenyl, aromatic C₆-C₁₄-carbocycle, 5- to 14-membered aromatic heterocycle or a 3- to 14-membered non-aromatic heterocycle, optionally in the presence of a base, and when appropriate in the presence of a transition metal catalyst such as a metal salt or complex and a ligand as described herein or by methods described in the literature (Heterocycles 1976, 4(8), 1331).

A compound of formula (I-d) wherein R^(8a) is a halogen atom can be converted in a compound of formula (I-e) wherein R^(8b) represents cyano, nitro, amino, mercapto, hydroxyl, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₂-C₆-alkenyloxy, C₂-C₆-haloalkenyloxy, C₃-C₈-cycloalkyl, C₃-C₆-cycloalkenyl, aromatic 5- to 14-membered heterocycle, C₃-C₈-cycloalkyloxy, aromatic C₆-C₁₄-carbocyclyloxy, non-aromatic 3- to 14-membered heterocyclyloxy, aromatic 5- to 14-membered heterocyclyloxy, —N(R^(h))₂ or —SR^(i) in the presence of a base and optionally in the presence of a transition metal catalyst such as a metal salt or complex, and if appropriate in the presence of a ligand.

A compound of formula (I-e) wherein R^(8b) is a C₂-C₆-alkenyl group can be further converted in a compound of formula (I-e) wherein R^(8b) is C₁-C₆-alkyl substituted by C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₁-C₆-alkoxy-C₁-C₆-alkoxy, C₁-C₆-alkylsulfanyl, C₁-C₆-haloalkylsulfanyl, non-aromatic 3- to 7-membered monocyclic heterocycle and —N(R^(a′))₂ with R^(a′) being independently selected from the group consisting of hydrogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl and C₃-C₈-cycloalkyl, by treating the reacting compound of formula (I-e) with an oxygen, a sulfur or an amino based nucleophile.

A compound of formula (I-e) wherein R^(8b) is a SR^(i) group can be further converted in a compound of formula (I-a-8) wherein R^(8b) is a —S(═O)R^(i) or a —S(═O)₂R^(i) group by reacting the starting compound of formula (I-a-8) with an oxidant such as hydrogen peroxide.

A compound of formula (I-a) can be prepared by one or more of the processes herein described.

Process M

A compound of formula (I-f) (i.e. formula (I) wherein T is —C(═O)R^(a1), —C(═O)(OR^(a1)), —C(═O)N(R^(a2))₂, —S(═O)R^(a1), —S(═O)₂R^(a1) and —S(═O)₂N(R^(a2))₂ with R^(a1) and R^(a2) being as described herein) can be prepared by a process comprising the step of reacting a compound of formula (I-a) formula with a compound of formula (32) as shown in scheme 13.

Process M can be performed by means of methods described in the literature (e.g. Tetrahedron Lett. 1995, 36, 8949; Greene's Protective Groups in organic Synthesis; Peter G. M. Wuts; Wiley; Fifth Edition; 2014; 1174-1175).

Compounds of formula (32) are commercially available.

Compounds of formula (I-a) can be prepared by one or more of the processes herein described.

Processes for the Preparation of a Compound of Formula (1)

A compound of formula (1) as described herein may be directly obtained by performing process N described below or may be obtained by conversion or derivatization of another compound of formula (1) prepared in accordance with the processes described herein. Compounds of formula (1-a)-(1-e) are various subsets of formula (1).

Process N

A compound of formula (1-a) (i.e. formula (1) wherein R⁷ and R⁸ are as defined in scheme 14) can be prepared by a process comprising the step of reacting a compound of formula (5) with a reagent of formula (8) as shown in scheme 14 in the presence of a base.

In scheme 14, R^(e) is as disclosed herein and R⁷, R⁸ and R^(e) may be substituted as disclosed herein.

Process N may be performed in the presence of suitable transition metal catalyst salts or complexes, if appropriate in the presence of a ligand.

The obtained compound of formula (1-a) can then be converted into a compound of formula (1-b) in one or more steps.

Non-limiting examples of such conversion are described below.

Compounds of formula (1-a) wherein U¹ is a C₁-C₆-alkoxy can be converted to compounds of formula (1-b) wherein U² is a hydroxyl group by well-known functional group interconversion methods, for example by hydrolysis of an ester group with LiOH in THF/water.

Compounds of formula (1-b) wherein U² is a hydroxyl can be converted to compounds of formula (1-b) wherein U² is a halogen in the presence of halogenating agents by well-known methods. Suitable halogenating reagents include, but are not limited to, phosphorous tribromide, phosphorous trichloride, phosphorous pentachloride, phosphorous trichloride oxide, oxalyl chloride or thionyl chloride.

Compounds of formula (1-b) wherein U² is a hydroxyl or halogen can be converted to compounds of formula (1-b) wherein U² is —N(CH₃)OCH₃ by well-known methods.

Compounds of formula (5) are commercially available or may be prepared by process Q described herein.

Compounds of formula (8) are commercially available or may be obtained by conversion or derivatization of another compound of formula (8) in accordance to well-known methods.

Process O

A compound of formula (1-c) (i.e. formula (1) wherein R⁷ is R^(7a) as defined in scheme 15) can be converted by means of known methods to the corresponding compounds of formula (1-d) (i.e. formula (1) wherein R⁷ is R^(7b) as defined in scheme 15) or (1-e) (i.e. formula (1) wherein R⁷ is R^(7c) as defined in scheme 15) in one or more steps as shown in scheme 15.

In scheme 15, R^(e), R^(f), R^(g) are as disclosed herein and the aliphatic and cyclic substituents R^(7b), R^(7c), R^(e), R^(f), R^(g) may be substituted as disclosed herein.

Non-limiting examples of conversion may be performed in accordance to the description provided in process K.

The obtained compound of formula (1-d) and (1-e) can then be converted into compound of formula (1-d) and (1-e) wherein U¹ (C₁-C₆-alkoxy) is replaced with hydroxyl or halogen.

Examples of such conversion are described below.

Compounds of formula (1-c), (1-d), (1-e) wherein U¹ is a C₁-C₆-alkoxy can be converted to compounds of formula (1-b), (1-c), (1-d) wherein U¹ is replaced with a hydroxyl group by well-known functional group interconversion methods, for example by hydrolysis of an ester group with LiOH in THF/water.

Compounds of formula (1-c), (1-d), (1-e) wherein U¹ has been replaced with a hydroxyl can then be further converted to compounds of formula (1-b), (1-c), (1-d) wherein the hydroxyl is replaced with a halogen in the presence of halogenating agents by well-known methods. Suitable halogenating reagents include, but are not limited to, phosphorous tribromide, phosphorous trichloride, phosphorous pentachloride, phosphorous trichloride oxide, oxalyl chloride or thionyl chloride.

Compounds of formula (1-c), (1-d), (1-e) wherein U¹ is a hydroxyl or halogen can be converted to compounds of formula (1-c), (1-d), (1-e) wherein U¹ is —N(CH₃)OCH₃ by well-known methods.

Compounds of formula (1-c) can be prepared by one or more of the processes described herein.

Process P

A compound of formula (1-f) (i.e. formula (1) wherein R⁸ is H) can be converted by means of methods described in the literature to the corresponding compound of formula (1-g) (i.e. formula (1) wherein R⁸ is R^(8a) as defined in scheme 16) or compound of formula (1-h) (i.e. formula (1) wherein R⁸ is R^(8a) as defined in scheme 16) in one or more steps as shown in scheme 16.

In scheme 16, R^(h) and R^(i) are as disclosed herein and the aliphatic and cyclic substituents R^(8a) and R^(8b) may be substituted as disclosed herein.

Non-limiting examples of conversion may be performed in accordance to the description provided in process L.

The obtained compound of formula (1-f) and (1-g) can then be converted into compound of formula (1-f) and (1-g) wherein U¹ (C₁-C₆-alkoxy) is replaced with hydroxyl or halogen.

Compounds of formula (1-f), (1-g), (1-h) wherein U¹ is a C₁-C₆-alkoxy can be converted to compounds of formula (1-f), (1-g), (1-h) wherein U¹ is replaced with a hydroxyl group by well-known functional group interconversion methods, for example by hydrolysis of an ester group with LiOH in THF/water.

Compounds of formula (1-f), (1-g), (1-h) wherein U¹ has been replaced with a hydroxyl can then be further converted to compounds of formula (1-f), (1-g), (1-h) wherein the hydroxyl is replaced with a halogen in the presence of halogenating agents by well-known methods. Suitable halogenating reagents include, but are not limited to, phosphorous tribromide, phosphorous trichloride, phosphorous pentachloride, phosphorous trichloride oxide, oxalyl chloride or thionyl chloride.

Compounds of formula (1-f), (1-g), (1-h) wherein U¹ is a hydroxyl or halogen can be converted to compounds of formula (1-f), (1-g), (1-h) wherein U¹ is —N(CH₃)OCH₃ by well-known methods.

Compounds (1-f) can be prepared by one or more of the processes described herein.

Process for the Preparation of Compound of Formula (5)

A compound of formula (5) as described herein may be commercially available or directly obtained by performing process Q described below. Compounds of formula (5-a) and (5-b) are various subsets of formula (5).

Process Q

A compound of formula (5-a) (i.e. compound of formula 5 wherein R⁷ is halogen) can be converted by means of known methods (WO2000044755) into a compound of formula (5-b) (i.e. compound of formula 5 wherein R⁷ is as shown in scheme 17) in the presence of either an oxygen (ethanol), a sulfur (thioethyl) or an amino (methylamine) based nucleophile, optionally in the presence of base as shown in scheme 17.

The compounds of formula (5-a) and (5-b) can be converted into compound of formula (5-a) and (5-b) wherein U¹ (C₁-C₆-alkoxy) is replaced with hydroxyl or halogen using the same conditions as described in process N.

Starting materials of formula (5-a) are commercially available.

Process for the Preparation of Compound of Formula (9) and (13)

A compound of formula (9) may be obtained by performing process R described below or may be obtained by conversion or derivatization of another compound of formula (9-a) prepared in accordance with the processes described herein. Compounds of formula (9-a) and (9-b) are various subsets of formula (9).

Process R

A compound of formula (9-a) can be converted by means of methods described in the literature to the corresponding compounds (13) in one or more steps as shown in scheme 18.

Compounds of formula (33) are commercially available or producible by processes described in the literature (Chemical & Pharmaceutical Bulletin 1977, 25(8), 1856-61).

A compound of formula (33) can be converted according to Step 1 of Process R into a compound of formula (9-a) in the presence of a reagent of formula (8) and a base (e.g organic or inorganic base) as described herein.

Non-limiting examples of conversion of (9-a) to (9-b) may be performed in accordance to scheme 18.

For example, a compound of formula (9-a) can be further converted in a compound of formula (9-b) wherein R⁷ is hydroxyl, mercapto, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₂-C₆-alkenyloxy, C₂-C₆-haloalkenyloxy, C₁-C₆-alkylsulfanyl, C₁-C₆-haloalkylsulfanyl, C₃-C₈-cycloalkyloxy, aromatic C₆-C₁₄-carbocyclyloxy, aromatic 5- or 6-membered monocyclic heterocyclyloxy, non-aromatic 3- to 7-membered monocyclic heterocyclyloxy, —N(R^(e))₂ by treating the reacting compound of formula (9-a) with an oxygen, a sulfur or an amino based nucleophile.

A compound of formula (9-a) can be converted into a compound of formula (9-b) wherein R⁷ is cyano, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl, C₃-C₈-cycloalkyl, C₃-C₆-cycloalkenyl, aromatic C₆-C₁₄-carbocycle, aromatic 5- or 6-membered monocyclic heterocycle, non-aromatic 3- to 7-membered monocyclic heterocycle by transition metal catalyzed or metallo-photoredox catalyzed processes as described herein.

An intermediate of formula (13) can be obtained according to Step 3 of Process R by treating a compound of formula (9) with a compound of formula (34) optionally in the presence of a base using well-known methods.

Compounds of formula (8) are commercially available or may be obtained by conversion or derivatization of another compound of formula (8) in accordance to well-known methods.

Process for the Preparation of Compounds of Formula (2), (19), (26-a-1)

Process S

A compound of formula (35) can be converted by means of methods described in the literature to the

corresponding compounds (2), (19-a), (19-b) and (26-a-1) in one or more steps as shown in scheme 19.

Aminoalcohols of formula (35) are commercially available or may be producible by methods described in the literature (Molecules, 9 (6), 405-426; 2004, WO2017203474).

The amino function of compound 35 is protected in accordance with known methods to provide compound of formula (19-a).

Subsequently, the compound of formula (19-a) can be converted by Step 2 of Process S into a compound of formula (2) using classical Mitsunobu reaction conditions known by the skilled person of the art (Strategic Applications of Named Reactions in Organic Synthesis; Laszlo Kürti, Barbara Czako; Elsevier; 2005; 294-295 and reference herein).

Compounds of formula (2) can be converted into compounds of formula (26-a-1) by well-known methods.

Compound (B)

The active compound combinations according to the invention comprise as compound (B) at least one further active compound selected from the following groups

-   -   (1) inhibitors of the ergosterol synthesis,     -   (2) inhibitors of the respiratory chain at complex I or II,     -   (3) inhibitors of the respiratory chain at complex III,     -   (4) inhibitors of the mitosis and cell division,     -   (5) compounds capable of having a multisite action,     -   (6) compounds capable of inducing a host defense,     -   (7) inhibitors of the amino acid and/or protein biosynthesis,     -   (8) inhibitors of the ATP production,     -   (9) inhibitors of the cell wall synthesis,     -   (10) inhibitors of the lipid and membrane synthesis,     -   (11) inhibitors of the melanine biosynthesis,     -   (12) inhibitors of the nucleic acid synthesis,     -   (13) inhibitors of the signal transduction,     -   (14) compounds capable of acting as uncoupler,     -   (15) other fungicides selected from the group consisting of         (15.001) abscisic acid, (15.002) benthiazole, (15.003)         bethoxazin, (15.004) capsimycin, (15.005) carvone, (15.006)         chinomethionat, (15.007) cufraneb, (15.008) cyflufenamid,         (15.009) cymoxanil, (15.010) cyprosulfamide, (15.011) flutianil,         (15.012) fosetyl-aluminium, (15.013) fosetyl-calcium, (15.014)         fosetyl-sodium, (15.015) methyl isothiocyanate, (15.016)         metrafenone, (15.017) mildiomycin, (15.018) natamycin, (15.019)         nickel dimethyldithiocarbamate, (15.020) nitrothal-isopropyl,         (15.021) oxamocarb, (15.022) oxathiapiprolin, (15.023)         oxyfenthiin, (15.024) pentachlorophenol and salts, (15.025)         phosphorous acid and its salts, (15.026) propamocarb-fosetylate,         (15.027) pyriofenone (chlazafenone), (15.028) tebufloquin,         (15.029) tecloftalam, (15.030) tolnifanide, (15.031)         1-(4-{4-[(5R)-5-(2,6-difluorophenyl)-4,5-dihydro-1,2-oxazol-3-yl]-1,3-thiazol-2-yl}piperidin-1-yl)-2-[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]ethanone,         (15.032)         1-(4-{4-[(5S)-5-(2,6-difluorophenyl)-4,5-dihydro-1,2-oxazol-3-yl]-1,3-thiazol-2-yl}piperidin-1-yl)-2-[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]ethanone,         (15.033) 2-(6-benzylpyridin-2-yl)quinazoline, (15.034)         dipymetitrone, (15.035)         2-[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]-1-[4-(4-{5-[2-(prop-2-yn-1-yloxy)phenyl]-4,5-dihydro-1,2-oxazol-3-yl}-1,3-thiazol-2-yl)piperidin-1-yl]ethanone,         (15.036)         2-[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]-1-[4-(4-{5-[2-chloro-6-(prop-2-yn-1-yloxy)phenyl]-4,5-dihydro-1,2-oxazol-3-yl}-1,3-thiazol-2-yl)piperidin-1-yl]ethanone,         (15.037)         2-[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]-1-[4-(4-{5-[2-fluoro-6-(prop-2-yn-1-yloxy)phenyl]-4,5-dihydro-1,2-oxazol-3-yl}-1,3-thiazol-2-yl)piperidin-1-yl]ethanone,         (15.038)         2-[6-(3-fluoro-4-methoxyphenyl)-5-methyl-pyridin-2-yl]quinazoline,         (15.039)         2-{(5R)-3-[2-(1-{[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4-yl]-4,5-dihydro-1,2-oxazol-5-yl}-3-chlorophenyl         methanesulfonate, (15.040)         2-{(5S)-3-[2-(1-{[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4-yl]-4,5-dihydro-1,2-oxazol-5-yl}-3-chlorophenyl         methanesulfonate, (15.041) ipflufenoquin, (15.042)         2-{2-fluoro-6-[(8-fluoro-2-methylquinolin-3-yl)oxy]phenyl}propan-2-ol,         (15.043) fluoxapiprolin, (15.044)         2-{3-[2-(1-{[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4-yl]-4,5-dihydro-1,2-oxazol-5-yl}phenyl         methanesulfonate, (15.045) 2-phenylphenol and salts, (15.046)         3-(4,4,5-trifluoro-3,3-dimethyl-3,4-dihydroisoquinolin-1-yl)quinoline,         (15.047) quinofumelin, (15.048) 4-amino-5-fluoropyrimidin-2-ol         (tautomeric form: 4-amino-5-fluoropyrimidin-2(1H)-one), (15.049)         4-oxo-4-[(2-phenylethyl)amino]butanoic acid, (15.050)         5-amino-1,3,4-thiadiazole-2-thiol, (15.051)         5-chloro-N′-phenyl-N′-(prop-2-yn-1-yl)thiophene-2-sulfonohydrazide,         (15.052) 5-fluoro-2-[(4-fluorobenzyl)oxy]pyrimidin-4-amine,         (15.053) 5-fluoro-2-[(4-methylbenzyl)oxy]pyrimidin-4-amine,         (15.054)         9-fluoro-2,2-dimethyl-5-(quinolin-3-yl)-2,3-dihydro-1,4-benzoxazepine,         (15.055) but-3-yn-1-yl         {6-[({[(Z)-(1-methyl-1H-tetrazol-5-yl)(phenyl)methylene]amino}oxy)methyl]pyridin-2-yl}carbamate,         (15.056) ethyl (2Z)-3-amino-2-cyano-3-phenylacrylate, (15.057)         phenazine-1-carboxylic acid, (15.058) propyl         3,4,5-trihydroxybenzoate, (15.059) quinolin-8-ol, (15.060)         quinolin-8-ol sulfate (2:1), (15.061) tert-butyl         {6-[({[(1-methyl-1H-tetrazol-5-yl)(phenyl)methylene]amino}oxy)methyl]pyridin-2-yl}carbamate,         (15.062)         5-fluoro-4-imino-3-methyl-1-[(4-methylphenyl)sulfonyl]-3,4-dihydropyri-midin-2(1H)-one,         (15.063) aminopyrifen, (15.064)         (N′-[2-chloro-4-(2-fluorophenoxy)-5-methylphenyl]-N-ethyl-N-methylimidoformamide),         (15.065)         (N′-(2-chloro-5-methyl-4-phenoxyphenyl)-N-ethyl-N-methylimidoformamide),         (15.066)         (2-{2-[(7,8-difluoro-2-methylquinolin-3-yl)oxy]-6-fluorophenyl}propan-2-ol),         (15.067)         (5-bromo-1-(5,6-dimethylpyridin-3-yl)-3,3-dimethyl-3,4-dihydroisoquinoline),         (15.068)         (3-(4,4-difluoro-5,5-dimethyl-4,5-dihydrothieno[2,3-c]pyridin-7-yl)quinoline),         (15.069)         (1-(4,5-dimethyl-1H-benzimidazol-1-yl)-4,4-difluoro-3,3-dimethyl-3,4-dihydroisoquinoline),         (15.070)         8-fluoro-3-(5-fluoro-3,3-dimethyl-3,4-dihydroisoquinolin-1-yl)quinolone,         (15.071)         8-fluoro-3-(5-fluoro-3,3,4,4-tetramethyl-3,4-dihydroisoquinolin-1-yl)quinolone,         (15.072)         3-(4,4-difluoro-3,3-dimethyl-3,4-dihydroisoquinolin-1-yl)-8-fluoroquinoline,         (15.073)         (N-methyl-N-phenyl-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide),         (15.074) methyl         {4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl}carbamate,         (15.075)         (N-{4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzyl}cyclopropanecarboxamide),         (15.076)         N-methyl-4-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide,         (15.077)         N-[(E)-methoxyiminomethyl]-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide,         (15.078)         N—[(Z)-methoxyiminomethyl]-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide,         (15.079)         N-[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]cyclopropanecarboxamide,         (15.080)         N-(2-fluorophenyl)-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide,         (15.081)         2,2-difluoro-N-methyl-2-[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]acetamide,         (15.082)         N-allyl-N-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)phenyl]methyl]acetamide,         (15.083)         N-[(E)-N-methoxy-C-methyl-carbonimidoyl]-4-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide,         (15.084)         N—[(Z)-N-methoxy-C-methyl-carbonimidoyl]-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide,         (15.085)         N-allyl-N-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]propanamide,         (15.086)         4,4-dimethyl-1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]-pyrrolidin-2-one,         (15.087)         N-methyl-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]-benzenecarbothioamide,         (15.088)         5-methyl-1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]pyrrolidin-2-one,         (15.089)         N-((2,3-difluoro-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]-3,3,3-trifluoro-propanamide,         (15.090)         1-methoxy-1-methyl-3-[[4-[5-(trifluoromethyl}-1,2,4-oxadiazol-3-yl]phenyl]methyl]urea,         (15.091)         1,1-diethyl-3-[[4-[5-(trifluoromethyl}-1,2,4-oxadiazol-3-yl]phenyl]methyl]urea,         (15.092)         N-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]propanamide,         (15.093)         N-methoxy-N-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]-methyl]cyclopropanecarboxamide,         (15.094)         1-methoxy-3-methyl-1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]urea,         (15.095)         N-methoxy-N-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl)cyclopropanecarboxamide,         (15.096)         N,2-dimethoxy-N-[[4-[5-(trifluoromethyl}-1,2,4-oxadiazol-3-yl]phenyl]-methyl]propanamide,         (15.097)         N-ethyl-2-methyl-N-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)phenyl]methyl]propanamide,         (15.098)         1-methoxy-3-methyl-1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]urea,         (15.099)         1,3-dimethoxy-1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]urea,         (15.100)         3-ethyl-1-methoxy-1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]urea,         (15.101)         1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]piperidin-2-one,         (15.102)         4,4-dimethyl-2-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]-methyl]isooxazolidin-3-one,         (15.103)         5,5-dimethyl-2-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]isoxazolidin-3-one,         (15.104)         3,3-dimethyl-1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]piperidin-2-one,         (15.105)         1-[[3-fluoro-4-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]azepan-2-one,         (15.106)         4,4-dimethyl-2-[[4-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]-methyl]isoxazolidin-3-one,         (15.107)         5,5-dimethyl-2-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]isoxazolidin-3-one,         (15.108) ethyl         1-{4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzyl}-1H-pyrazole-4-carboxylate,         (15.109)         N,N-dimethyl-1-{4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzyl}-1H-1,2,4-triazol-3-amine,         (15.110)         N-{2,3-difluoro-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzyl}butanamide,         (15.111)         N-(1-methylcyclopropyl)-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide,         (15.112)         N-(2,4-difluorophenyl)-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide,         (15.113)         1-(5,6-dimethylpyridin-3-yl)-4,4-difluoro-3,3-dimethyl-3,4-dihydroisoquinoline,         (15.114)         1-(6-(difluoromethyl)-5-methyl-pyridin-3-yl)-4,4-difluoro-3,3-dimethyl-3,4-dihydroisoquinoline,         (15.115)         1-(5-(fluoromethyl)-6-methyl-pyridin-3-yl)-4,4-difluoro-3,3-dimethyl-3,4-dihydroisoquinoline,         (15.116)         1-(6-(difluoromethyl)-5-methoxy-pyridin-3-yl)-4,4-difluoro-3,3-dimethyl-3,4-dihydroisoquinoline,         (15.117) 4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl         dimethylcarbamate, (15.118)         N-{4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl}propanamide,         (15.119)         3-[2-(1-{[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4-yl]-1,5-dihydro-2,4-benzodioxepin-6-yl         methanesulfonate, (15.120)         9-fluoro-3-[2-(1-{[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4-yl]-1,5-dihydro-2,4-benzodioxepin-6-yl         methanesulfonate, (15.121)         3-[2-(1-{[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4-yl]-1,5-dihydro-2,4-benzodioxepin-6-yl         methanesulfonate, (15.122)         3-[2-(1-{[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4-yl]-9-fluoro-1,5-dihydro-2,4-benzodioxepin-6-yl         methanesulfonate, (15.123)         1-(6,7-dimethylpyrazolo[1,5-a]pyridin-3-yl)-4,4-difluoro-3,3-dimethyl-3,4-dihydroisoquinoline,         (15.124)         8-fluoro-N-(4,4,4-trifluoro-2-methyl-1-phenylbutan-2-yl)quinoline-3-carboxamide,         (15.125)         8-fluoro-N-[(2S)-4,4,4-trifluoro-2-methyl-1-phenylbutan-2-yl]quinoline-3-carboxamide,         (15.126)         N-(2,4-dimethyl-1-phenylpentan-2-yl)-8-fluoroquinoline-3-carboxamide,         (15.127)         N-[(2S)-2,4-dimethyl-1-phenylpentan-2-yl]-8-fluoroquinoline-3-carboxamide,         (15.128) D-tagatose.     -   (16) Antibacterial agents selected from the group of:         -   bacteria, such as (16.001) Bacillus subtilis, in particular             strain QST713/AQ713 (available as SERENADE OPTI or SERENADE             ASO from Bayer CropScience LP, US, having NRRL Accession No.             B21661 and described in U.S. Pat. No. 6,060,051); (16.002)             Bacillus amyloliquefaciens, in particular strain D747             (available as Double Nickel™ from Certis, US, having             accession number FERM BP-8234 and disclosed in U.S. Pat. No.             7,094,592); (16.003) Bacillus pumilus, in particular strain             BU F-33 (having NRRL Accession No. 50185); (16.004) Bacillus             subtilis var. amyloliquefaciens strain FZB24 (available as             Taegro® from Novozymes, US); (16.005) a Paenibacillus sp.             strain having Accession No. NRRL B-50972 or Accession No.             NRRL B-67129 and described in International Patent             Publication No. WO 2016/154297; and         -   fungi, such as (16.006) Aureobasidium pullulans, in             particular blastospores of strain DSM14940; 16.007)             Aureobasidium pullulans blastospores of strain DSM 14941;             (16.008) Aureobasidium pullulans, in particular mixtures of             blastospores of strains DSM14940 and DSM14941;     -   (17) biological fungicides selected from the group of:         -   bacteria, for example (17.001) Bacillus subtilis, in             particular strain QST713/AQ713 (available as SERENADE OPTI             or SERENADE ASO from Bayer CropScience LP, US, having NRRL             Accession No. B21661 and described in U.S. Pat. No.             6,060,051); (17.002) Bacillus pumilus, in particular strain             QST2808 (available as SONATA® from Bayer CropScience LP, US,             having Accession No. NRRL B-30087 and described in U.S. Pat.             No. 6,245,551); (17.003) Bacillus pumilus, in particular             strain GB34 (available as Yield Shield® from Bayer AG, DE);             (17.004) Bacillus pumilus, in particular strain BU F-33             (having NRRL Accession No. 50185); (17.005) Bacillus             amyloliquefaciens, in particular strain D747 (available as             Double Nickel™ from Certis, US, having accession number FERM             BP-8234 and disclosed in U.S. Pat. No. 7,094,592); (17.006)             Bacillus subtilis Y1336 (available as BIOBAC® WP from             Bion-Tech, Taiwan, registered as a biological fungicide in             Taiwan under Registration Nos. 4764, 5454, 5096 and 5277);             (17.007) Bacillus amyloliquefaciens strain MBI 600             (available as SUBTILEX from BASF SE); (17.008) Bacillus             subtilis strain GB03 (available as Kodiak® from Bayer AG,             DE); (17.009) Bacillus subtilis var. amyloliquefaciens             strain FZB24 (available from Novozymes Biologicals Inc.,             Salem, Virginia or Syngenta Crop Protection, LLC,             Greensboro, North Carolina as the fungicide TAEGRO® or             TAEGRO® ECO (EPA Registration No. 70127-5); (17.010)             Bacillus mycoides, isolate J (available as BmJ TGAI or WG             from Certis USA); (17.011) Bacillus licheniformis, in             particular strain SB3086 (available as EcoGuard™Biofungicide             and Green Releaf from Novozymes); (17.012) a Paenibacillus             sp. strain having Accession No. NRRL B-50972 or Accession             No. NRRL B-67129 and described in International Patent             Publication No. WO 2016/154297,     -   (18) fatty acids or derivatives,         -   for example (18.001) a composition comprising one or more             fatty acids or derivatives thereof selected from unsaturated             and saturated C₁₂-C₂₄ fatty acids, salts thereof, esters             thereof or mixtures of any of the foregoing, wherein at             least 95% of said fatty acids or derivatives thereof are in             the range of C₁₄ to C₂₀ (e.g. FLiPPER by AlphaBio Pesticides             or Bayer AG).

Compound (B) is preferably selected from:

inhibitors of the ergosterol biosynthesis selected from the group consisting of (1.001) cyproconazole, (1.002) difenoconazole, (1.003) epoxiconazole, (1.004) fenhexamid, (1.005) fenpropidin, (1.006) fenpropimorph, (1.007) fenpyrazamine, (1.008) fluquinconazole, (1.009) flutriafol, (1.010) imazalil, (1.011) imazalil sulfate, (1.012) ipconazole, (1.013) metconazole, (1.014) myclobutanil, (1.015) paclobutrazol, (1.016) prochloraz, (1.017) propiconazole, (1.018) prothioconazole, (1.019) pyrisoxazole, (1.020) spiroxamine, (1.021) tebuconazole, (1.022) tetraconazole, (1.023) triadimenol, (1.024) tridemorph, (1.025) triticonazole, (1.026) (1R,2S,5S)-5-(4-chlorobenzyl)-2-(chloromethyl)-2-methyl-1-(1H-1,2,4-triazol-1-ylmethyl)cyclopentanol, (1.027) (1S,2R,5R)-5-(4-chlorobenzyl)-2-(chloromethyl)-2-methyl-1-(1H-1,2,4-triazol-1-ylmethyl)cyclopentanol, (1.028) (2R)-2-(1-chlorocyclopropyl)-4-[(1R)-2,2-dichlorocyclopropyl]-1-(1H-1,2,4-triazol-1-yl)butan-2-ol, (1.029) (2R)-2-(1-chlorocyclopropyl)-4-[(1S)-2,2-dichlorocyclopropyl]-1-(1H-1,2,4-triazol-1-yl)butan-2-ol, (1.030) (2R)-2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1-(1H-1,2,4-triazol-1-yl)propan-2-ol, (1.031) (2S)-2-(1-chlorocyclopropyl)-4-[(1R)-2,2-dichlorocyclopropyl]-1-(1H-1,2,4-triazol-1-yl)butan-2-ol, (1.032) (2S)-2-(1-chlorocyclopropyl)-4-[(1S)-2,2-dichlorocyclopropyl]-1-(1H-1,2,4-triazol-1-yl)butan-2-ol, (1.033) (2S)-2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1-(1H-1,2,4-triazol-1-yl)propan-2-ol, (1.034) (R)-[3-(4-chloro-2-fluorophenyl)-5-(2,4-difluorophenyl)-1,2-oxazol-4-yl](pyridin-3-yl)methanol, (1.035) (S)-[3-(4-chloro-2-fluorophenyl)-5-(2,4-difluorophenyl)-1,2-oxazol-4-yl](pyridin-3-yl)methanol, (1.036) [3-(4-chloro-2-fluorophenyl)-5-(2,4-difluorophenyl)-1,2-oxazol-4-yl](pyridin-3-yl)methanol, (1.037) 1-({(2R,4S)-2-[2-chloro-4-(4-chlorophenoxy)phenyl]-4-methyl-1,3-dioxolan-2-yl}methyl)-1H-1,2,4-triazole, (1.038) 1-({(2S,4S)-2-[2-chloro-4-(4-chlorophenoxy)phenyl]-4-methyl-1,3-dioxolan-2-yl}methyl)-1H-1,2,4-triazole, (1.039) 1-{[3-(2-chlorophenyl)-2-(2,4-difluoro-phenyl)oxiran-2-yl]methyl}-1H-1,2,4-triazol-5-yl thiocyanate, (1.040) 1-{[rel(2R,3R)-3-(2-chlorophenyl)-2-(2,4-difluorophenyl)oxiran-2-yl]methyl}-1H-1,2,4-triazol-5-yl thiocyanate, (1.041) 1-{[rel(2R,3S)-3-(2-chlorophenyl)-2-(2,4-difluorophenyl)oxiran-2-yl]methyl}-1H-1,2,4-triazol-5-yl thiocyanate, (1.042) 2-[(2R,4R,5R)-1-(2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazole-3-thione, (1.043) 2-[(2R,4R,5S)-1-(2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazole-3-thione, (1.044) 2-[(2R,4S,5R)-1-(2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazole-3-thione, (1.045) 2-[(2R,4S,5S)-1-(2,4-dichloro-phenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazole-3-thione, (1.046) 2-[(2S,4R,5R)-1-(2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazole-3-thione, (1.047) 2-[(2S,4R,5S)-1-(2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazole-3-thione, (1.048) 2-[(2S,4S,5R)-1-(2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazole-3-thione, (1.049) 2-[(2S,4S,5S)-1-(2,4-dichloro-phenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazole-3-thione, (1.050) 2-[1-(2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazole-3-thione, (1.051) 2-[2-chloro-4-(2,4-dichlorophenoxy)phenyl]-1-(1H-1,2,4-triazol-1-yl)propan-2-ol, (1.052) 2-[2-chloro-4-(4-chlorophenoxy)phenyl]-1-(1H-1,2,4-triazol-1-yl)butan-2-ol, (1.053) 2-[4-(4-chlorophenoxy)-2-(trifluoro-methyl)phenyl]-1-(1H-1,2,4-triazol-1-yl)butan-2-ol, (1.054) 2-[4-(4-chlorophenoxy)-2-(trifluoro-methyl)phenyl]-1-(1H-1,2,4-triazol-1-yl)pentan-2-ol, (1.055) mefentrifluconazole, (1.056) 2-{[3-(2-chloro-phenyl)-2-(2,4-difluorophenyl)oxiran-2-yl]methyl}-2,4-dihydro-3H-1,2,4-triazole-3-thione, (1.057) 2-{[rel(2R,3R)-3-(2-chlorophenyl)-2-(2,4-difluorophenyl)oxiran-2-yl]methyl}-2,4-dihydro-3H-1,2,4-tria-zole-3-thione, (1.058) 2-{[rel(2R,3S)-3-(2-chlorophenyl)-2-(2,4-difluorophenyl)oxiran-2-yl]methyl}-2,4-dihydro-3H-1,2,4-triazole-3-thione, (1.059) 5-(4-chlorobenzyl)-2-(chloromethyl)-2-methyl-1-(JH-1,2,4-triazol-1-ylmethyl)cyclopentanol, (1.060) 5-(allylsulfanyl)-1-{[3-(2-chlorophenyl)-2-(2,4-difluoro-phenyl)oxiran-2-yl]methyl}-1H-1,2,4-triazole, (1.061) 5-(allylsulfanyl)-1-{[rel(2R,3R)-3-(2-chlorophenyl)-2-(2,4-difluorophenyl)oxiran-2-yl]methyl-1H-1,2,4-triazole, (1.062) 5-(allylsulfanyl)-1-{[rel(2R,3S)-3-(2-chlorophenyl)-2-(2,4-difluorophenyl)oxiran-2-yl]methyl}-1H-1,2,4-triazole, (1.063) N′-(2,5-dimethyl-4-{[3-(1,1,2,2-tetrafluoroethoxy)phenyl]sulfanyl}phenyl)-N-ethyl-N-methylimidoformamide, (1.064) N′-(2,5-dimethyl-4-{[3-(2,2,2-trifluoroethoxy)phenyl]sulfanyl}phenyl)N-ethyl-N-methylimidoformamide, (1.065) N′-(2,5-dimethyl-4-{[3-(2,2,3,3-tetrafluoropropoxy)phenyl]sulfanyl}phenyl)-N-ethyl-N-methylimidoformamide, (1.066) N′-(2,5-dimethyl-4-{[3-(pentafluoroethoxy)phenyl]sulfanyl}phenyl)-N-ethyl-N-methylimidoformamide, (1.067) N′-(2,5-dimethyl-4-{3-[(1,1,2,2-tetrafluoroethyl)sulfanyl]-phenoxy}phenyl)-N-ethyl-N-methylimidoformamide, (1.068) N′-(2,5-dimethyl-4-{3-[(2,2,2-trifluoro-ethyl)sulfanyl]phenoxy}phenyl)-N-ethyl-N-methylimidoformamide, (1.069) N′-(2,5-dimethyl-4-{3-[(2,2,3,3-tetrafluoropropyl)sulfanyl]phenoxy}phenyl)-N-ethyl-N-methylimidoformamide, (1.070) N′-(2,5-dimethyl-4-{3-[(pentafluoroethyl)sulfanyl]phenoxy}phenyl)-N-ethyl-N-methylimidoformamide, (1.071) N′-(2,5-dimethyl-4-phenoxyphenyl)-N-ethyl-N-methylimidoformamide, (1.072) N′-(4-{[3-(difluoro-methoxy)phenyl]sulfanyl}-2,5-dimethylphenyl)-N-ethyl-N-methylimidoformamide, (1.073) N′-(4-{3-[(difluoromethyl)sulfanyl]phenoxy}-2,5-dimethylphenyl)-N-ethyl-N-methylimidoformamide, (1.074) N′-[5-bromo-6-(2,3-dihydro-1H-inden-2-yloxy)-2-methylpyridin-3-yl]-N-ethyl-N-methylimidoformamide, (1.075) N′-{4-[(4,5-dichloro-1,3-thiazol-2-yl)oxy]-2,5-dimethylphenyl}-N-ethyl-N-methylimidoformamide, (1.076) N′-{5-bromo-6-[(1R)-1-(3,5-difluorophenyl)ethoxy]-2-methylpyridin-3-yl}-N-ethyl-N-methylimidoformamide, (1.077) N′-{5-bromo-6-[(1S)-1-(3,5-difluorophenyl)ethoxy]-2-methylpyridin-3-yl}-N-ethyl-N-methylimidoformamide, (1.078) N′-{5-bromo-6-[(cis-4-isopropylcyclohexyl)oxy]-2-methylpyridin-3-yl-N-ethyl-N-methylimidoformamide, (1.079) N′-{5-bromo-6-[(trans-4-isopropylcyclo-hexyl)oxy]-2-methylpyridin-3-yl}-N-ethyl-N-methylimidoformamide, (1.080) N′-{5-bromo-6-[1-(3,5-difluorophenyl)ethoxy]-2-methylpyridin-3-yl}-N-ethyl-N-methylimidoformamide, (1.081) ipfentrifluconazole, (1.082) 2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1-(1H-1,2,4-triazol-1-yl)propan-2-ol, (1.083) 2-[6-(4-bromophenoxy)-2-(trifluoromethyl)-3-pyridyl]-1-(1,2,4-triazol-1-yl)propan-2-ol, (1.084) 2-[6-(4-chlorophenoxy)-2-(trifluoromethyl)-3-pyridyl]-1-(1,2,4-triazol-1-yl)propan-2-ol, (1.085) 3-[2-(1-chlorocyclopropyl)-3-(3-chloro-2-fluoro-phenyl)-2-hydroxy-propyl]imidazole-4-carbonitrile, (1.086) 4-[[6-[rac-(2R)-2-(2,4-difluorophenyl)-1,1-difluoro-2-hydroxy-3-(5-thioxo-4H-1,2,4-triazol-1-yl)propyl]-3-pyridyl]oxy]benzonitrile, (1.087) N-isopropyl-N′-[5-methoxy-2-methyl-4-(2,2,2-trifluoro-1-hydroxy-1-phenylethyl)phenyl]-N-methylimidoformamide, (1.088) N′-{5-bromo-2-methyl-6-[(1-propoxypropan-2-yl)oxy]pyridin-3-yl}-N-ethyl-N-methylimidoformamide, (1.089) hexaconazole, (1.090) penconazole, (1.091) fenbuconazole, (1.092) methyl 2-[2-chloro-4-(4-chlorophenoxy)phenyl]-2-hydroxy-3-(1,2,4-triazol-1-yl)propanoate inhibitors of the respiratory chain at complex I or II selected from the group consisting of (2.001) benzovindiflupyr, (2.002) bixafen, (2.003) boscalid, (2.004) carboxin, (2.005) fluopyram, (2.006) flutolanil, (2.007) fluxapyroxad, (2.008) furametpyr, (2.009) Isofetamid, (2.010) isopyrazam (anti-epimeric enantiomer 1R,4S,9S), (2.011) isopyrazam (anti-epimeric enantiomer 1S,4R,9R), (2.012) isopyrazam (anti-epimeric racemate 1RS,4SR,9SR), (2.013) isopyrazam (mixture of syn-epimeric racemate 1RS,4SR,9RS and anti-epimeric racemate 1RS,4SR,9SR), (2.014) isopyrazam (syn-epimeric enantiomer 1R,4S,9R), (2.015) isopyrazam (syn-epimeric enantiomer 1S,4R,9S), (2.016) isopyrazam (syn-epimeric racemate 1RS,4SR,9RS), (2.017) penflufen, (2.018) penthiopyrad, (2.019) pydiflumetofen, (2.020) Pyraziflumid, (2.021) sedaxane, (2.022) 1,3-dimethyl-N-(1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl)-1H-pyrazole-4-carboxamide, (2.023) 1,3-dimethyl-N-[(3R)-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl]-1H-pyrazole-4-carboxamide, (2.024) 1,3-dimethyl-N-[(3S)-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl]-1H-pyrazole-4-carboxamide, (2.025) 1-methyl-3-(trifluoromethyl)-N-[2′-(trifluoromethyl)biphenyl-2-yl]-1H-pyrazole-4-carboxamide, (2.026) 2-fluoro-6-(trifluoromethyl)-N-(1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl)benzamide, (2.027) 3-(difluoromethyl)-1-methyl-N-(1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl)-1H-pyrazole-4-carboxamide, (2.028) inpyrfluxam, (2.029) 3-(difluoromethyl)-1-methyl-N-[(3S)-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl]-1H-pyrazole-4-carboxamide, (2.030) fluindapyr, (2.031) 3-(difluoromethyl)-N-[(3R)-7-fluoro-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl]-1-methyl-1H-pyrazole-4-carboxamide, (2.032) 3-(difluoromethyl)-N-[(3S)-7-fluoro-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl]-1-methyl-1H-pyrazole-4-carboxamide, (2.033) 5,8-difluoro-N-[2-(2-fluoro-4-{[4-(trifluoromethyl)pyridin-2-yl]oxy}phenyl)ethyl]quinazolin-4-amine, (2.034) N-(2-cyclopentyl-5-fluorobenzyl)-N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.035) N-(2-tert-butyl-5-methylbenzyl)-N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.036) N-(2-tert-butylbenzyl)-N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.037) N-(5-chloro-2-ethylbenzyl)-N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.038) isoflucypram, (2.039) N-[(1R,4S)-9-(dichloromethylene)-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl]-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide, (2.040) N-[(1S,4R)-9-(dichloromethylene)-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl]-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide, (2.041) N-[1-(2,4-dichlorophenyl)-1-methoxypropan-2-yl]-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide, (2.042) N-[2-chloro-6-(trifluoromethyl)benzyl]-N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.043) N-[3-chloro-2-fluoro-6-(trifluoromethyl)benzyl]-N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.044) N-[5-chloro-2-(trifluoromethyl)benzyl]-N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.045) N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl-N-[5-methyl-2-(trifluoromethyl)benzyl]-1H-pyrazole-4-carboxamide, (2.046) N-cyclopropyl-3-(difluoromethyl)-5-fluoro-N-(2-fluoro-6-isopropylbenzyl)-1-methyl-1H-pyrazole-4-carboxamide, (2.047) N-cyclopropyl-3-(difluoromethyl)-5-fluoro-N-(2-isopropyl-5-methylbenzyl)-1-methyl-1H-pyrazole-4-carboxamide, (2.048) N-cyclopropyl-3-(difluoromethyl)-5-fluoro-N-(2-isopropylbenzyl)-1-methyl-1H-pyrazole-4-carbothioamide, (2.049) N-cyclopropyl-3-(difluoromethyl)-5-fluoro-N-(2-isopropylbenzyl)-1-methyl-1H-pyrazole-4-carboxamide, (2.050) N-cyclopropyl-3-(difluoromethyl)-5-fluoro-N-(5-fluoro-2-isopropylbenzyl)-1-methyl-1H-pyrazole-4-carboxamide, (2.051) N-cyclopropyl-3-(difluoromethyl)-N-(2-ethyl-4,5-dimethylbenzyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.052) N-cyclopropyl-3-(difluoromethyl)-N-(2-ethyl-5-fluorobenzyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.053) N-cyclopropyl-3-(difluoromethyl)-N-(2-ethyl-5-methylbenzyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.054) N-cyclopropyl-N-(2-cyclopropyl-5-fluorobenzyl)-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.055) N-cyclopropyl-N-(2-cyclopropyl-5-methylbenzyl)-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.056) N-cyclopropyl-N-(2-cyclopropylbenzyl)-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.057) pyrapropoyne, (2.058) N-[rac-(1S,2S)-2-(2,4-dichlorophenyl)cyclobutyl]-2-(trifluoromethyl)nicotinamide, (2.059) N-[(1S,2S)-2-(2,4-dichlorophenyl)cyclobutyl]-2-(trifluoromethyl)nicotinamide, (2.060) flubene-teram, inhibitors of the respiratory chain at complex III selected from the group consisting of (3.001) ametoctradin, (3.002) amisulbrom, (3.003) azoxystrobin, (3.004) coumethoxystrobin, (3.005) coumoxystrobin, (3.006) cyazofamid, (3.007) dimoxystrobin, (3.008) enoxastrobin, (3.009) famoxadone, (3.010) fenamidone, (3.011) flufenoxystrobin, (3.012) fluoxastrobin, (3.013) kresoxim-methyl, (3.014) metominostrobin, (3.015) orysastrobin, (3.016) picoxystrobin, (3.017) pyraclostrobin, (3.018) pyrametostrobin, (3.019) pyraoxystrobin, (3.020) trifloxystrobin, (3.021) (2E)-2-{2-[({[(1E)-1-(3-{[(E)-1-fluoro-2-phenyl-vinyl]oxy}phenyl)ethylidene]amino}oxy)methyl]phenyl}-2-(methoxyimino)-N-methylacetamide, (3.022) (2E,3Z)-5-{[1-(4-chlorophenyl)-1H-pyrazol-3-yl]oxy}-2-(methoxyimino)-N,3-dimethylpent-3-enamide, (3.023) (2R)-2-{2-[(2,5-dimethylphenoxy)methyl]phenyl}-2-methoxy-N-methylacetamide, (3.024) (2S)-2-{2-[(2,5-dimethylphenoxy)methyl]phenyl}-2-methoxy-N-methylacetamide, (3.025) fenpicoxamid, (3.026) mandestrobin, (3.027) N-(3-ethyl-3,5,5-trimethylcyclohexyl)-3-formamido-2-hydroxybenzamide, (3.028) (2E,3Z)-5-{[1-(4-chloro-2-fluorophenyl)-1H-pyrazol-3-yl]oxy}-2-(methoxyimino)-N,3-dimethylpent-3-enamide, (3.029) methyl {5-[3-(2,4-dimethylphenyl)-1H-pyrazol-1-yl]-2-methylbenzyl}carbamate, (3.030) metyltetraprole, (3.031) florylpicoxamid, (3.032) (2S,3S)-3-(o-tolyl)butan-2-yl N-{[4-methoxy-3-(propa-noyloxy)-2-pyridyl]carbonyl}-L-alaninate, inhibitors of the mitosis and cell division selected from the group consisting of (4.001) carbendazim, (4.002) diethofencarb, (4.003) ethaboxam, (4.004) fluopicolide, (4.005) pencycuron, (4.006) thiabendazole, (4.007) thiophanate-methyl, (4.008) zoxamide, (4.009) pyridachlometyl, (4.010) 3-chloro-5-(4-chlorophenyl)-4-(2,6-difluorophenyl)-6-methylpyridazine, (4.011) 3-chloro-5-(6-chloropyridin-3-yl)-6-methyl-4-(2,4,6-trifluorophenyl)pyridazine, (4.012) 4-(2-bromo-4-fluorophenyl)-N-(2,6-difluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.013) 4-(2-bromo-4-fluorophenyl)-N-(2-bromo-6-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.014) 4-(2-bromo-4-fluorophenyl)-N-(2-bromophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.015) 4-(2-bromo-4-fluorophenyl)-N-(2-chloro-6-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.016) 4-(2-bromo-4-fluorophenyl)-N-(2-chlorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.017) 4-(2-bromo-4-fluorophenyl)-N-(2-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.018) 4-(2-chloro-4-fluorophenyl)-N-(2,6-difluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.019) 4-(2-chloro-4-fluorophenyl)-N-(2-chloro-6-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.020) 4-(2-chloro-4-fluorophenyl)-N-(2-chlorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.021) 4-(2-chloro-4-fluorophenyl)-N-(2-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.022) 4-(4-chlorophenyl)-5-(2,6-difluorophenyl)-3,6-dimethylpyridazine, (4.023) N-(2-bromo-6-fluorophenyl)-4-(2-chloro-4-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.024) N-(2-bromophenyl)-4-(2-chloro-4-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.025) N-(4-chloro-2,6-difluorophenyl)-4-(2-chloro-4-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.026) fluopimomide, compounds capable to have a multisite action selected from the group consisting of (5.001) bordeaux mixture, (5.002) captafol, (5.003) captan, (5.004) chlorothalonil, (5.005) copper hydroxide, (5.006) copper naphthenate, (5.007) copper oxide, (5.008) copper oxychloride, (5.009) copper(2+) sulfate, (5.010) dithianon, (5.011) dodine, (5.012) folpet, (5.013) mancozeb, (5.014) maneb, (5.015) metiram, (5.016) metiram zinc, (5.017) oxine-copper, (5.018) propineb, (5.019) sulfur and sulfur preparations including calcium polysulfide, (5.020) thiram, (5.021) zineb, (5.022) ziram, (5.023) 6-ethyl-5,7-dioxo-6,7-dihydro-5H-pyrrolo[3′,4′:5,6][1,4]dithiino[2,3-c][1,2]thiazole-3-carbonitrile, compounds capable to induce a host defence selected from the group consisting of (6.001) acibenzolar-S-methyl, (6.002) isotianil, (6.003) probenazole, (6.004) tiadinil, inhibitors of the amino acid and/or protein biosynthesis selected from the group consisting of (7.001) cyprodinil, (7.002) kasugamycin, (7.003) kasugamycin hydrochloride hydrate, (7.004) oxytetracycine, (7.005) pyrimethanil, (7.006) 3-(5-fluoro-3,3,4,4-tetramethyl-3,4-dihydroisoquinolin-1-yl)quinoline, inhibitors of the ATP production selected from the group consisting of (8.001) silthiofam, inhibitors of the cell wall synthesis selected from the group consisting of (9.001) benthiavalicarb, (9.002) dimethomorph, (9.003) flumorph, (9.004) iprovalicarb, (9.005) mandipropamid, (9.006) pyrimorph, (9.007) valifenalate, (9.008) (2E)-3-(4-tert-butylphenyl)-3-(2-chloropyridin-4-yl)-1-(morpholin-4-yl)prop-2-en-1-one, (9.009) (2Z)-3-(4-tert-butylphenyl)-3-(2-chloropyridin-4-yl)-1-(morpholin-4-yl)prop-2-en-1-one, inhibitors of the lipid and membrane synthesis selected from the group consisting of (10.001) propamocarb, (10.002) propamocarb hydrochloride, (10.003) tolclofos-methyl, inhibitors of the melanin biosynthesis selected from the group consisting of (11.001) tricyclazole, (11.002) tolprocarb, inhibitors of the nucleic acid synthesis selected from the group consisting of (12.001) benalaxyl, (12.002) benalaxyl-M (kiralaxyl), (12.003) metalaxyl, (12.004) metalaxyl-M (mefenoxam), inhibitors of the signal transduction selected from the group consisting of (13.001) fludioxonil, (13.002) iprodione, (13.003) procymidone, (13.004) proquinazid, (13.005) quinoxyfen, (13.006) vinclozolin, compounds capable to act as an uncoupler selected from the group consisting of (14.001) fluazinam, (14.002) meptyldinocap, further fungicides selected from the group consisting of (15.001) abscisic acid, (15.002) benthiazole, (15.003) bethoxazin, (15.004) capsimycin, (15.005) carvone, (15.006) chinomethionat, (15.007) cufraneb, (15.008) cyflufenamid, (15.009) cymoxanil, (15.010) cyprosulfamide, (15.011) flutianil, (15.012) fosetyl-aluminium, (15.013) fosetyl-calcium, (15.014) fosetyl-sodium, (15.015) methyl isothiocyanate, (15.016) metrafenone, (15.017) mildiomycin, (15.018) natamycin, (15.019) nickel dimethyldithiocarbamate, (15.020) nitrothal-isopropyl, (15.021) oxamocarb, (15.022) oxathiapiprolin, (15.023) oxyfenthiin, (15.024) pentachlorophenol and salts, (15.025) phosphorous acid and its salts, (15.026) propamocarb-fosetylate, (15.027) pyriofenone (chlazafenone), (15.028) tebufloquin, (15.029) tecloftalam, (15.030) tolnifanide, (15.031) 1-(4-{4-[(5R)-5-(2,6-difluorophenyl)-4,5-dihydro-1,2-oxazol-3-yl]-1,3-thiazol-2-yl}piperidin-1-yl)-2-[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]ethanone, (15.032) 1-(4-{4-[(5S)-5-(2,6-difluorophenyl)-4,5-dihydro-1,2-oxazol-3-yl]-1,3-thiazol-2-yl}piperidin-1-yl)-2-[5-methyl-3-(trifluoro-methyl)-1H-pyrazol-1-yl]ethanone, (15.033) 2-(6-benzylpyridin-2-yl)quinazoline, (15.034) dipymetitrone, (15.035) 2-[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]-1-[4-(4-{5-[2-(prop-2-yn-1-yloxy)phenyl]-4,5-dihydro-1,2-oxazol-3-yl}-1,3-thiazol-2-yl)piperidin-1-yl]ethanone, (15.036) 2-[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]-1-[4-(4-{5-[2-chloro-6-(prop-2-yn-1-yloxy)phenyl]-4,5-dihydro-1,2-oxazol-3-yl}-1,3-thiazol-2-yl)piperidin-1-yl]ethanone, (15.037) 2-[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]-1-[4-(4-{5-[2-fluoro-6-(prop-2-yn-1-yloxy)phenyl]-4,5-dihydro-1,2-oxazol-3-yl}-1,3-thiazol-2-yl)piperidin-1-yl]ethanone, (15.038) 2-[6-(3-fluoro-4-methoxyphenyl)-5-methylpyridin-2-yl]quinazoline, (15.039) 2-{(5R)-3-[2-(1-{[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4-yl]-4,5-dihydro-1,2-oxazol-5-yl}-3-chlorophenyl methanesulfonate, (15.040) 2-{(5S)-3-[2-(1-{[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4-yl]-4,5-dihydro-1,2-oxazol-5-yl}-3-chlorophenyl methanesulfonate, (15.041) ipflufenoquin, (15.042) 2-{2-fluoro-6-[(8-fluoro-2-methylquinolin-3-yl)oxy]phenyl}propan-2-ol, (15.043) fluoxapiprolin, (15.044) 2-{3-[2-(1-{[3,5-bis(difluoromethyl)-11H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4-yl]-4,5-dihydro-1,2-oxazol-5-yl}phenyl methanesulfonate, (15.045) 2-phenylphenol and salts, (15.046) 3-(4,4,5-trifluoro-3,3-dimethyl-3,4-dihydroisoquinolin-1-yl)quinoline, (15.047) quinofumelin, (15.048) 4-amino-5-fluoropyrimidin-2-ol (tautomeric form: 4-amino-5-fluoropyrimidin-2(1H)-one), (15.049) 4-oxo-4-[(2-phenyl-ethyl)amino]butanoic acid, (15.050) 5-amino-1,3,4-thiadiazole-2-thiol, (15.051) 5-chloro-N′-phenyl-N′-(prop-2-yn-1-yl)thiophene-2-sulfonohydrazide, (15.052) 5-fluoro-2-[(4-fluorobenzyl)oxy]pyrimidin-4-amine, (15.053) 5-fluoro-2-[(4-methylbenzyl)oxy]pyrimidin-4-amine, (15.054) 9-fluoro-2,2-dimethyl-5-(quinolin-3-yl)-2,3-dihydro-1,4-benzoxazepine, (15.055) but-3-yn-1-yl {6-[({[(Z)-(1-methyl-1H-tetrazol-5-yl)(phenyl)methylene]amino}oxy)methyl]pyridin-2-yl}carbamate, (15.056) ethyl (2Z)-3-amino-2-cyano-3-phenylacrylate, (15.057) phenazine-1-carboxylic acid, (15.058) propyl 3,4,5-trihydroxybenzoate, (15.059) quinolin-8-ol, (15.060) quinolin-8-ol sulfate (2:1), (15.061) tert-butyl {6-[({[(1-methyl-1H-tetrazol-5-yl)(phenyl)methylene]amino}oxy)methyl]pyridin-2-yl}carbamate, (15.062) 5-fluoro-4-imino-3-methyl-1-[(4-methylphenyl)sulfonyl]-3,4-dihydropyrimidin-2(1H)-one, (15.063) aminopyrifen, (15.064) (N′-[2-chloro-4-(2-fluorophenoxy)-5-methylphenyl]-N-ethyl-N-methylimidoformamide), (15.065) (N′-(2-chloro-5-methyl-4-phenoxyphenyl)-N-ethyl-N-methylimidoformamide), (15.066) (2-{2-[(7,8-difluoro-2-methylquinolin-3-yl)oxy]-6-fluorophenyl}propan-2-ol), (15.067) (5-bromo-1-(5,6-dimethylpyridin-3-yl)-3,3-dimethyl-3,4-dihydroisoquinoline), (15.068) (3-(4,4-difluoro-5,5-dimethyl-4,5-dihydrothieno[2,3-c]pyridin-7-yl)quinoline), (15.069) (1-(4,5-dimethyl-1H-benzimidazol-1-yl)-4,4-difluoro-3,3-dimethyl-3,4-dihydroisoquinoline), (15.070) 8-fluoro-3-(5-fluoro-3,3-dimethyl-3,4-dihydroisoquinolin-1-yl)quinolone, (15.071) 8-fluoro-3-(5-fluoro-3,3,4,4-tetramethyl-3,4-dihydroisoquinolin-1-yl)quinolone, (15.072) 3-(4,4-difluoro-3,3-dimethyl-3,4-dihydroisoquinolin-1-yl)-8-fluoroquinoline, (15.073) (N-methyl-N-phenyl-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide), (15.074) methyl {4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl}carbamate, (15.075) (N-{4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzyl}-cyclopropanecarboxamide), (15.076) N-methyl-4-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide, (15.077) N-[(E)-methoxyiminomethyl]-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide, (15.078) N-[(Z)-methoxyiminomethyl]-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide, (15.079) N-[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]cyclopropanecarboxamide, (15.080) N-(2-fluorophenyl)-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide, (15.081) 2,2-difluoro-N-methyl-2-[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]acetamide, (15.082) N-allyl-N-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)phenyl]methyl]acetamide, (15.083) N-[(E)-N-methoxy-C-methyl-carbonimidoyl]-4-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide, (15.084) N—[(Z)-N-methoxy-C-methyl-carbonimidoyl]-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide, (15.085) N-allyl-N-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]propanamide, (15.086) 4,4-dimethyl-1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]pyrrolidin-2-one, (15.087) N-methyl-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzenecarbothioamide, (15.088) 5-methyl-1-[[4-[5-(trifluoro-methyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]pyrrolidin-2-one, (15.089) N-((2,3-difluoro-4-[5-(trifluoro-methyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]-3,3,3-trifluoro-propanamide, (15.090) 1-methoxy-1-methyl-3-[[4-[5-(trifluoromethyl}-1,2,4-oxadiazol-3-yl]phenyl]methyl]urea, (15.091) 1,1-diethyl-3-[[4-[5-(trifluoromethyl}-1,2,4-oxadiazol-3-yl]phenyl]methyl]urea, (15.092) N-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]propanamide, (15.093) N-methoxy-N-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]cyclopropanecarboxamide, (15.094) 1-methoxy-3-methyl-1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]urea, (15.095) N-methoxy-N-[[4-[5-(trifluoro-methyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl)cyclopropanecarboxamide, (15.096) N,2-dimethoxy-N-[[4-[5-(trifluoromethyl}-1,2,4-oxadiazol-3-yl]phenyl]methyl]propanamide, (15.097) N-ethyl-2-methyl-N-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)phenyl]methyl]propanamide, (15.098) 1-methoxy-3-methyl-1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]urea, (15.099) 1,3-dimethoxy-1-[[4-[5-(trifluoro-methyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]urea, (15.100) 3-ethyl-1-methoxy-1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]urea, (15.101) 1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]-methyl]piperidin-2-one, (15.102) 4,4-dimethyl-2-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]-methyl]isooxazolidin-3-one, (15.103) 5,5-dimethyl-2-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]isoxazolidin-3-one, (15.104) 3,3-dimethyl-1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]piperidin-2-one, (15.105) 1-[[3-fluoro-4-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]-phenyl]methyl]azepan-2-one, (15.106) 4,4-dimethyl-2-[[4-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]-phenyl]methyl]isoxazolidin-3-one, (15.107) 5,5-dimethyl-2-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]-phenyl]methyl]isoxazolidin-3-one, (15.108) ethyl 1-{4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzyl}-1H-pyrazole-4-carboxylate, (15.109) N,N-dimethyl-1-{4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzyl}-1H-1,2,4-triazol-3-amine, (15.110) N-{2,3-difluoro-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzyl}butanamide, (15.111) N-(1-methylcyclopropyl)-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide, (15.112) N-(2,4-difluorophenyl)-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide, (15.113) 1-(5,6-dimethylpyridin-3-yl)-4,4-difluoro-3,3-dimethyl-3,4-dihydroisoquinoline, (15.114) 1-(6-(difluoromethyl)-5-methyl-pyridin-3-yl)-4,4-difluoro-3,3-dimethyl-3,4-dihydroisoquinoline, (15.115) 1-(5-(fluoromethyl)-6-methyl-pyridin-3-yl)-4,4-difluoro-3,3-dimethyl-3,4-dihydroisoquinoline, (15.116) 1-(6-(difluoromethyl)-5-methoxy-pyridin-3-yl)-4,4-difluoro-3,3-dimethyl-3,4-dihydroisoquinoline, (15.117) 4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl dimethylcarbamate, (15.118) N-{4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl}propanamide, (15.119) 3-[2-(1-{[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4-yl]-1,5-dihydro-2,4-benzodioxepin-6-yl methanesulfonate, (15.120) 9-fluoro-3-[2-(1-{[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4-yl]-1,5-dihydro-2,4-benzodioxepin-6-yl methanesulfonate, (15.121) 3-[2-(1-{[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4-yl]-1,5-dihydro-2,4-benzodioxepin-6-yl methanesulfonate, (15.122) 3-[2-(1-{[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4-yl]-9-fluoro-1,5-dihydro-2,4-benzodioxepin-6-yl methanesulfonate, (15.123) 1-(6,7-dimethylpyrazolo[1,5-a]pyridin-3-yl)-4,4-difluoro-3,3-dimethyl-3,4-dihydroisoquinoline, (15.124) 8-fluoro-N-(4,4,4-trifluoro-2-methyl-1-phenylbutan-2-yl)quinoline-3-carboxamide, (15.125) 8-fluoro-N-[(2S)-4,4,4-trifluoro-2-methyl-1-phenylbutan-2-yl]quinoline-3-carboxamide, (15.126) N-(2,4-dimethyl-1-phenylpentan-2-yl)-8-fluoroquinoline-3-carboxamide, (15.127) N-[(2S)-2,4-dimethyl-1-phenylpentan-2-yl]-8-fluoroquinoline-3-carboxamide, (15.128) D-tagatose, antibacterial agents selected from the group consisting of bacteria, such as (16.001) Bacillus subtilis, in particular strain QST713/AQ713 (available as SERENADE OPTI or SERENADE ASO from Bayer CropScience LP, US, having NRRL Accession No. B21661 and described in U.S. Pat. No. 6,060,051); (16.002) Bacillus amyloliquefaciens, in particular strain D747 (available as Double Nickel™ from Certis, US, having accession number FERM BP-8234 and disclosed in U.S. Pat. No. 7,094,592); (16.003) Bacillus pumilus, in particular strain BU F-33 (having NRRL Accession No. 50185); (16.004) Bacillus subtilis var. amyloliquefaciens strain FZB24 (available as Taegro® from Novozymes, US); (16.005) a Paenibacillus sp. strain having Accession No. NRRL B-50972 or Accession No. NRRL B-67129 and described in International Patent Publication No. WO 2016/154297; and fungi, such as (16.006) Aureobasidium pullulans, in particular blastospores of strain DSM14940; (16.007) Aureobasidium pullulans blastospores of strain DSM 14941; (16.008) Aureobasidium pullulans, in particular mixtures of blastospores of strains DSM14940 and DSM14941, biological fungicides selected from the group consisting of bacteria, for example (17.001) Bacillus subtilis, in particular strain QST713/AQ713 (available as SERENADE OPTI or SERENADE ASO from Bayer CropScience LP, US, having NRRL Accession No. B21661 and described in U.S. Pat. No. 6,060,051); (17.002) Bacillus pumilus, in particular strain QST2808 (available as SONATA® from Bayer CropScience LP, US, having Accession No. NRRL B-30087 and described in U.S. Pat. No. 6,245,551); (17.003) Bacillus pumilus, in particular strain GB34 (available as Yield Shield® from Bayer AG, DE); (17.004) Bacillus pumilus, in particular strain BU F-33 (having NRRL Accession No. 50185); (17.005) Bacillus amyloliquefaciens, in particular strain D747 (available as Double Nickel™ from Certis, US, having accession number FERM BP-8234 and disclosed in U.S. Pat. No. 7,094,592); (17.006) Bacillus subtilis Y1336 (available as BIOBAC® WP from Bion-Tech, Taiwan, registered as a biological fungicide in Taiwan under Registration Nos. 4764, 5454, 5096 and 5277); (17.007) Bacillus amyloliquefaciens strain MBI 600 (available as SUBTILEX from BASF SE); (17.008) Bacillus subtilis strain GB03 (available as Kodiak® from Bayer AG, DE); (17.009) Bacillus subtilis var. amyloliquefaciens strain FZB24 (available from Novozymes Biologicals Inc., Salem, Virginia or Syngenta Crop Protection, LLC, Greensboro, North Carolina as the fungicide TAEGRO® or TAEGRO® ECO (EPA Registration No. 70127-5); (17.010) Bacillus mycoides, isolate J (available as BmJ TGAI or WG from Certis USA); (17.011) Bacillus licheniformis, in particular strain SB3086 (available as EcoGuard™ Biofungicide and Green Releaf from Novozymes); (17.012) a Paenibacillus sp. strain having Accession No. NRRL B-50972 or Accession No. NRRL B-67129 and described in International Patent Publication No. WO 2016/154297, fatty acids or derivatives, for example (18.001) a composition comprising one or more fatty acids or derivatives thereof selected from unsaturated and saturated C₁₂-C₂₄ fatty acids, salts thereof, esters thereof or mixtures of any of the foregoing, wherein at least 95% of said fatty acids or derivatives thereof are in the range of C₁₄ to C₂₀ (e.g. FLiPPER by AlphaBio Pesticides or Bayer AG).

Compound (B) is more preferably selected from:

(1.001) cyproconazole, (1.002) difenoconazole, (1.003) epoxiconazole, (1.004) fenhexamid, (1.010) imazalil, (1.012) ipconazole, (1.013) metconazole, (1.017) propiconazole, (1.018) prothioconazole, (1.020) spiroxamine, (1.021) tebuconazole, (1.026) (1R,2S,5S)-5-(4-chlorobenzyl)-2-(chloromethyl)-2-methyl-1-(1H-1,2,4-triazol-1-ylmethyl)cyclopentanol, (1.027) (1S,2R,5R)-5-(4-chlorobenzyl)-2-(chloromethyl)-2-methyl-1-(JH-1,2,4-triazol-1-ylmethyl)cyclopentanol, (1.055) mefentrifluconazole, (1.059) 5-(4-chlorobenzyl)-2-(chloromethyl)-2-methyl-1-(1H-1,2,4-triazol-1-ylmethyl)cyclopentanol, (1.062) fluoxytio-conazole, (1.067) N′-(2,5-dimethyl-4-{3-[(1,1,2,2-tetrafluoro-ethyl)sulfanyl]-phenoxy}phenyl)-N-ethyl-N-methyl-imidoformamide, (1.081) ipfentrifluconazole, (1.082) 2-[6-(4-bromophenoxy)-2-(trifluoro-methyl)-3-pyridyl]-1-(1,2,4-triazol-1-yl)propan-2-ol and (1.092) methyl 2-[2-chloro-4-(4-chloro-phenoxy)phenyl]-2-hydroxy-3-(1,2,4-triazol-1-yl)propanoate (2.001) benzovindiflupyr, (2.002) bixafen, (2.003) boscalid, (2.005) fluopyram, (2.007) fluxapyroxad, (2.009) isofetamid, (2.010) isopyrazam (anti-epimeric enantiomer 1R,4S,9S), (2.011) isopyrazam (anti-epimeric enantiomer 1S,4R,9R), (2.012) isopyrazam (anti-epimeric racemate 1RS,4SR,9SR), (2.013) isopyrazam (mixture of syn-epimeric racemate 1RS,4SR,9RS and anti-epimeric racemate 1RS,4SR,9SR), (2.014) isopyrazam (syn-epimeric enantiomer 1R,4S,9R), (2.015) isopyrazam (syn-epimeric enantiomer 1S,4R,9S), (2.016) isopyrazam (syn-epimeric racemate 1RS,4SR,9RS), (2.017) penflufen, (2.018) penthiopyrad, (2.019) pydiflumetofen, (2.021) sedaxane, (2.028) inpyrfluxam, (2.030) fluindapyr, (2.038) isoflucypram, (3.003) azoxystrobin, (3.007) dimoxystrobin, (3.012) fluoxastrobin, (3.013) kresoxim-methyl, (3.016) picoxystrobin, (3.017) pyraclostrobin, (3.020) trifloxystrobin, (3.025) fenpicoxamid, (3.026) 2-{2-[(2,5-dimethylphenoxy)methyl]phenyl}-2-methoxy-N-methylacetamide, (3.030) metyltetraprole, (3.031) florylpicoxamid, (4.005) pencycuron, (4.007) thiophanate-methyl, (4.012) 4-(2-bromo-4-fluorophenyl)-N-(2,6-difluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.015) 4-(2-bromo-4-fluorophenyl)-N-(2-chloro-6-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.025) N-(4-chloro-2,6-difluorophenyl)-4-(2-chloro-4-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (5.003) captan, (5.004) chlorothalonil, (5.010), dithianon, (5.011) dodine, (5.012) folpet, (5.013) mancozeb, (5.015) metiram, (5.018) propineb, (6.002) isotianil, (7.001) cyprodinil, (7.005) pyrimethanil, (12.003) metalaxyl, (12.004) metalaxyl-M (mefenoxam), (13.001) fludioxonil, (13.002) iprodione, (13.004) proquinazid, (13.005) quinoxyfen, (14.001) fluazinam, (14.002) meptyldinocap, (15.008) cyflufenamid, (15.010) cyprosulfamide, (15.011) flutianil, (15.012) fosetyl-aluminium, (15.016) metrafenone, (15.027) pyriofenone (chlazafenone), (15.043) fluoxa-piprolin (15.047) 3-(4,4-difluoro-3,3-dimethyl-3,4-dihydroisoquinolin-1-yl)quinolone, (15.048) 4-amino-5-fluoropyrimidin-2-ol (tautomeric form: 4-amino-5-fluoropyrimidin-2(1H)-one), (15.052) 5-fluoro-2-[(4-fluorobenzyl)oxy]pyrimidin-4-amine, (15.053) 5-fluoro-2-[(4-methylbenzyl)oxy]pyrimidin-4-amine, (15.062) 5-fluoro-4-imino-3-methyl-1-[(4-methylphenyl)sulfonyl]-3,4-dihydropyrimidin-2(1H)-one, (15.063) aminopyrifen, (15.064) (N′-[2-chloro-4-(2-fluorophenoxy)-5-methylphenyl]-N-ethyl-N-methylimidoformamide), (16.001) Bacillus subtilis, in particular strain QST713/AQ713 (available as SERENADE OPTI or SERENADE ASO from Bayer CropScience LP, US, having NRRL Accession No. B21661 and described in U.S. Pat. No. 6,060,051), (17.001) Bacillus subtilis, in particular strain QST713/AQ713 (available as SERENADE OPTI or SERENADE ASO from Bayer CropScience LP, US, having NRRL Accession No. B21661 and described in U.S. Pat. No. 6,060,051); (17.002) Bacillus pumilus, in particular strain QST2808 (available as SONATA® from Bayer CropScience LP, US, having Accession No. NRRL B-30087 and described in U.S. Pat. No. 6,245,551); (17.003) Bacillus pumilus, in particular strain GB34 (available as Yield Shield® from Bayer AG, DE); (17.008) Bacillus subtilis strain GB03 (available as Kodiak® from Bayer AG, DE); (17.009) Bacillus subtilis var. amyloliquefaciens strain FZB24 (available from Novozymes Biologicals Inc., Salem, Virginia or Syngenta Crop Protection, LLC, Greensboro, North Carolina as the fungicide TAEGRO® or TAEGRO® ECO (EPA Registration No. 70127-5); (17.011) Bacillus licheniformis, in particular strain SB3086 (available as EcoGuard™ Biofungicide and Green Releaf from Novozymes); (17.012) a Paenibacillus sp. strain having Accession No. NRRL B-50972 or Accession No. NRRL B-67129 and described in International Patent Publication No. WO 2016/154297, (18.001) a composition comprising one or more fatty acids or derivatives thereof selected from unsaturated and saturated C₁₂-C₂₄ fatty acids, salts thereof, esters thereof or mixtures of any of the foregoing, wherein at least 95% of said fatty acids or derivatives thereof are in the range of C₁₄ to C₂₀ (e.g. FLiPPER by AlphaBio Pesticides or Bayer AG).

Compound (B) is likewise more preferably selected from:

(1.001) cyproconazole, (1.002) difenoconazole, (1.003) epoxiconazole, (1.004) fenhexamid, (1.010) imazalil, (1.012) ipconazole, (1.013) metconazole, (1.017) propiconazole, (1.018) prothioconazole, (1.020) spiroxamine, (1.021) tebuconazole, (1.026) (1R,2S,5S)-5-(4-chlorobenzyl)-2-(chloromethyl)-2-methyl-1-(1H-1,2,4-triazol-1-ylmethyl)cyclopentanol, (1.027) (1S,2R,5R)-5-(4-chlorobenzyl)-2-(chloromethyl)-2-methyl-1-(1H-1,2,4-triazol-1-ylmethyl)cyclopentanol, (1.055) mefentrifluconazole, (1.059) 5-(4-chlorobenzyl)-2-(chloromethyl)-2-methyl-1-(1H-1,2,4-triazol-1-ylmethyl)cyclopentanol, (1.081) ipfentrifluconazole, (1.082) 2-[6-(4-bromophenoxy)-2-(trifluoromethyl)-3-pyridyl]-1-(1,2,4-triazol-1-yl)propan-2-ol and (1.092) methyl 2-[2-chloro-4-(4-chlorophenoxy)phenyl]-2-hydroxy-3-(1,2,4-triazol-1-yl)propanoate (2.001) benzovindiflupyr, (2.002) bixafen, (2.003) boscalid, (2.005) fluopyram, (2.007) fluxapyroxad, (2.009) isofetamid, (2.010) isopyrazam (anti-epimeric enantiomer 1R,4S,9S), (2.011) isopyrazam (anti-epimeric enantiomer 1S,4R,9R), (2.012) isopyrazam (anti-epimeric racemate 1RS,4SR,9SR), (2.013) isopyrazam (mixture of syn-epimeric racemate 1RS,4SR,9RS and anti-epimeric racemate 1RS,4SR,9SR), (2.014) isopyrazam (syn-epimeric enantiomer 1R,4S,9R), (2.015) isopyrazam (syn-epimeric enantiomer 1S,4R,9S), (2.016) isopyrazam (syn-epimeric racemate 1RS,4SR,9RS), (2.017) penflufen, (2.018) penthiopyrad, (2.019) pydiflumetofen, (2.021) sedaxane, (2.028) inpyrfluxam, (2.030) fluindapyr, (2.038) isoflucypram, (3.003) azoxystrobin, (3.007) dimoxystrobin, (3.012) fluoxastrobin, (3.013) kresoxim-methyl, (3.016) picoxystrobin, (3.017) pyraclostrobin, (3.020) trifloxystrobin, (3.025) fenpicoxamid, (3.026) 2-{2-[(2,5-dimethylphenoxy)methyl]phenyl}-2-methoxy-N-methylacetamide, (3.030) metyltetraprole, (3.031) florylpicoxamid, (4.005) pencycuron, (4.007) thiophanate-methyl, (4.012) 4-(2-bromo-4-fluorophenyl)-N-(2,6-difluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.015) 4-(2-bromo-4-fluorophenyl)-N-(2-chloro-6-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.025) N-(4-chloro-2,6-difluorophenyl)-4-(2-chloro-4-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (5.003) captan, (5.004) chlorothalonil, (5.010), dithianon, (5.011) dodine, (5.012) folpet, (5.013) mancozeb, (5.015) metiram, (5.018) propineb, (6.002) isotianil, (7.001) cyprodinil, (7.005) pyrimethanil, (12.003) metalaxyl, (12.004) metalaxyl-M (mefenoxam), (13.001) fludioxonil, (13.002) iprodione, (13.004) proquinazid, (13.005) quinoxyfen, (14.001) fluazinam, (14.002) meptyldinocap, (15.008) cyflufenamid, (15.010) cyprosulfamide, (15.011) flutianil, (15.012) fosetyl-aluminium, (15.016) metrafenone, (15.027) pyriofenone (chlazafenone), (15.047) 3-(4,4-difluoro-3,3-dimethyl-3,4-dihydroisoquinolin-1-yl)quinolone, (15.048) 4-amino-5-fluoropyrimidin-2-ol (tautomeric form: 4-amino-5-fluoropyrimidin-2(1H)-one), (15.052) 5-fluoro-2-[(4-fluorobenzyl)oxy]pyrimidin-4-amine, (15.053) 5-fluoro-2-[(4-methylbenzyl)oxy]pyrimidin-4-amine, (15.062) 5-fluoro-4-imino-3-methyl-1-[(4-methylphenyl)sulfonyl]-3,4-dihydropyrimidin-2(1H)-one, (15.063) aminopyrifen, (15.064) (N′-[2-chloro-4-(2-fluorophenoxy)-5-methylphenyl]-N-ethyl-N-methylimidoformamide), (16.001) Bacillus subtilis, in particular strain QST713/AQ713 (available as SERENADE OPTI or SERENADE ASO from Bayer CropScience LP, US, having NRRL Accession No. B21661 and described in U.S. Pat. No. 6,060,051), (17.001) Bacillus subtilis, in particular strain QST713/AQ713 (available as SERENADE OPTI or SERENADE ASO from Bayer CropScience LP, US, having NRRL Accession No. B21661 and described in U.S. Pat. No. 6,060,051); (17.002) Bacillus pumilus, in particular strain QST2808 (available as SONATA® from Bayer CropScience LP, US, having Accession No. NRRL B-30087 and described in U.S. Pat. No. 6,245,551); (17.003) Bacillus pumilus, in particular strain GB34 (available as Yield Shield® from Bayer AG, DE); (17.008) Bacillus subtilis strain GB03 (available as Kodiak® from Bayer AG, DE); (17.009) Bacillus subtilis var. amyloliquefaciens strain FZB24 (available from Novozymes Biologicals Inc., Salem, Virginia or Syngenta Crop Protection, LLC, Greensboro, North Carolina as the fungicide TAEGRO® or TAEGRO® ECO (EPA Registration No. 70127-5); (17.011) Bacillus licheniformis, in particular strain SB3086 (available as EcoGuard™ Biofungicide and Green Releaf from Novozymes); (17.012) a Paenibacillus sp. strain having Accession No. NRRL B-50972 or Accession No. NRRL B-67129 and described in International Patent Publication No. WO 2016/154297, (18.001) a composition comprising one or more fatty acids or derivatives thereof selected from unsaturated and saturated C₁₂-C₂₄ fatty acids, salts thereof, esters thereof or mixtures of any of the foregoing, wherein at least 95% of said fatty acids or derivatives thereof are in the range of C₁₄ to C₂₀ (e.g. FLiPPER by AlphaBio Pesticides or Bayer AG).

Compound (B) is even more preferably selected from:

(1.002) difenoconazole, (1.004) fenhexamid, (1.010) imazalil, (1.012) ipconazole, (1.018) prothioconazole, (1.020) spiroxamine, (1.021) tebuconazole, (1.026) (1R,2S,5S)-5-(4-chlorobenzyl)-2-(chloromethyl)-2-methyl-1-(1H-1,2,4-triazol-1-ylmethyl)cyclopentanol, (1.027) (1S,2R,5R)-5-(4-chlorobenzyl)-2-(chloromethyl)-2-methyl-1-(1H-1,2,4-triazol-1-ylmethyl)cyclopentanol, (1.055) mefentrifluconazole, (1.059) 5-(4-chlorobenzyl)-2-(chloromethyl)-2-methyl-1-(1H-1,2,4-triazol-1-ylmethyl)cyclopentanol, (1.062) fluoxy¬tio¬conazole, (1.067) N′-(2,5-dimethyl-4-{3-[(1,1,2,2-tetrafluoroethyl)sulfanyl]¬phenoxy}phenyl)-N-ethyl-N-methyl¬imido¬formamide, (1.081) ipfentrifluconazole, (1.082) 2-[6-(4-bromophenoxy)-2-(trifluoromethyl)-3-pyridyl]-1-(1,2,4-triazol-1-yl)propan-2-ol and (1.092) methyl 2-[2-chloro-4-(4-chlorophenoxy)phenyl]-2-hydroxy-3-(1,2,4-triazol-1-yl)propanoate (2.001) benzovindiflupyr, (2.002) bixafen, (2.003) boscalid, (2.005) fluopyram, (2.007) fluxapyroxad, (2.017) penflufen, (2.018) penthiopyrad, (2.019) pydiflumetofen, (2.021) sedaxane, (2.028) inpyrfluxam, (2.030) fluindapyr, (2.038) isoflucypram, (3.003) azoxystrobin, (3.012) fluoxastrobin, (3.016) picoxystrobin, (3.017) pyraclostrobin, (3.020) trifloxystrobin, (3.025) fenpicoxamid, (3.026) 2-{2-[(2,5-dimethylphenoxy)methyl]phenyl}-2-methoxy-N-methylacetamide, (3.030) metyltetraprole, (3.031) florylpicoxamid, (4.005) pencycuron, (4.007) thiophanate-methyl, (4.012) 4-(2-bromo-4-fluorophenyl)-N-(2,6-difluoro-phenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.015) 4-(2-bromo-4-fluorophenyl)-N-(2-chloro-6-fluoro-phenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.025) N-(4-chloro-2,6-difluorophenyl)-4-(2-chloro-4-fluoro-phenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (5.003) captan, (5.004) chlorothalonil, (5.010), dithianon, (5.012) folpet, (5.013) mancozeb, (5.015) metiram, (5.018) propineb, (6.002) isotianil, (7.005) pyrimethanil, (12.003) metalaxyl, (12.004) metalaxyl-M (mefenoxam), (13.001) fludioxonil, (13.004) proquinazid, (13.005) quinoxyfen, (14.001) fluazinam, (14.002) meptyldinocap, (15.008) cyflufenamid, (15.012) fosetyl-aluminium, (15.016) metrafenone, (15.027) pyriofenone (chlazafenone), (15.043) fluoxa-piprolin, (15.047) 3-(4,4-difluoro-3,3-dimethyl-3,4-dihydroisoquinolin-1-yl)quinolone, (15.048) 4-amino-5-fluoropyrimidin-2-ol (tautomeric form: 4-amino-5-fluoropyrimidin-2(1H)-one), (15.052) 5-fluoro-2-[(4-fluorobenzyl)oxy]pyrimidin-4-amine, (15.062) 5-fluoro-4-imino-3-methyl-1-[(4-methylphenyl)sulfonyl]-3,4-dihydropyrimidin-2(1H)-one, (15.064) (N′-[2-chloro-4-(2-fluorophenoxy)-5-methylphenyl]-N-ethyl-N-methylimidoformamide), (16.001) Bacillus subtilis, in particular strain QST713/AQ713 (available as SERENADE OPTI or SERENADE ASO from Bayer CropScience LP, US, having NRRL Accession No. B21661 and described in U.S. Pat. No. 6,060,051), (17.001) Bacillus subtilis, in particular strain QST713/AQ713 (available as SERENADE OPTI or SERENADE ASO from Bayer CropScience LP, US, having NRRL Accession No. B21661 and described in U.S. Pat. No. 6,060,051); (17.012) a Paenibacillus sp. strain having Accession No. NRRL B-50972 or Accession No. NRRL B-67129 and described in International Patent Publication No. WO 2016/154297, (18.001) a composition comprising one or more fatty acids or derivatives thereof selected from unsaturated and saturated C₁₂-C₂₄ fatty acids, salts thereof, esters thereof or mixtures of any of the foregoing, wherein at least 95% of said fatty acids or derivatives thereof are in the range of C₁₄ to C₂₀ (e.g. FLiPPER by AlphaBio Pesticides or Bayer AG).

Compound (B) is likewise even more preferably selected from:

(1.002) difenoconazole, (1.004) fenhexamid, (1.010) imazalil, (1.012) ipconazole, (1.018) prothioconazole, (1.020) spiroxamine, (1.021) tebuconazole, (1.026) (1R,2S,5S)-5-(4-chlorobenzyl)-2-(chloromethyl)-2-methyl-1-(1H-1,2,4-triazol-1-ylmethyl)cyclopentanol, (1.027) (1S,2R,5R)-5-(4-chlorobenzyl)-2-(chloromethyl)-2-methyl-1-(1H-1,2,4-triazol-1-ylmethyl)cyclopentanol, (1.055) mefentrifluconazole, (1.059) 5-(4-chlorobenzyl)-2-(chloromethyl)-2-methyl-1-(1H-1,2,4-triazol-1-ylmethyl)cyclopentanol, (1.081) ipfentrifluconazole, (1.082) 2-[6-(4-bromophenoxy)-2-(trifluoromethyl)-3-pyridyl]-1-(1,2,4-triazol-1-yl)propan-2-ol and (1.092) methyl 2-[2-chloro-4-(4-chlorophenoxy)phenyl]-2-hydroxy-3-(1,2,4-triazol-1-yl)propanoate (2.001) benzovindiflupyr, (2.002) bixafen, (2.003) boscalid, (2.005) fluopyram, (2.007) fluxapyroxad, (2.017) penflufen, (2.018) penthiopyrad, (2.019) pydiflumetofen, (2.021) sedaxane, (2.028) inpyrfluxam, (2.030) fluindapyr, (2.038) isoflucypram, (3.003) azoxystrobin, (3.012) fluoxastrobin, (3.016) picoxystrobin, (3.017) pyraclostrobin, (3.020) trifloxystrobin, (3.025) fenpicoxamid, (3.026) 2-{2-[(2,5-dimethylphenoxy)methyl]phenyl}-2-methoxy-N-methylacetamide, (3.030) metyltetraprole, (3.031) florylpicoxamid, (4.005) pencycuron, (4.007) thiophanate-methyl, (4.012) 4-(2-bromo-4-fluorophenyl)-N-(2,6-difluoro-phenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.015) 4-(2-bromo-4-fluorophenyl)-N-(2-chloro-6-fluoro-phenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.025) N-(4-chloro-2,6-difluorophenyl)-4-(2-chloro-4-fluoro-phenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (5.003) captan, (5.004) chlorothalonil, (5.010), dithianon, (5.012) folpet, (5.013) mancozeb, (5.015) metiram, (5.018) propineb, (6.002) isotianil, (7.005) pyrimethanil, (12.003) metalaxyl, (12.004) metalaxyl-M (mefenoxam), (13.001) fludioxonil, (13.004) proquinazid, (13.005) quinoxyfen, (14.001) fluazinam, (14.002) meptyldinocap, (15.008) cyflufenamid, (15.012) fosetyl-aluminium, (15.016) metrafenone, (15.027) pyriofenone (chlazafenone), (15.047) 3-(4,4-difluoro-3,3-dimethyl-3,4-dihydroisoquinolin-1-yl)quinolone, (15.048) 4-amino-5-fluoropyrimidin-2-ol (tautomeric form: 4-amino-5-fluoropyrimidin-2(1H)-one), (15.052) 5-fluoro-2-[(4-fluorobenzyl)oxy]pyrimidin-4-amine, (15.062) 5-fluoro-4-imino-3-methyl-1-[(4-methyl-phenyl)sulfonyl]-3,4-dihydropyrimidin-2(1H)-one, (15.064) (N′-[2-chloro-4-(2-fluorophenoxy)-5-methylphenyl]-N-ethyl-N-methylimidoformamide), (16.001) Bacillus subtilis, in particular strain QST713/AQ713 (available as SERENADE OPTI or SERENADE ASO from Bayer CropScience LP, US, having NRRL Accession No. B21661 and described in U.S. Pat. No. 6,060,051), (17.001) Bacillus subtilis, in particular strain QST713/AQ713 (available as SERENADE OPTI or SERENADE ASO from Bayer CropScience LP, US, having NRRL Accession No. B21661 and described in U.S. Pat. No. 6,060,051); (17.012) a Paenibacillus sp. strain having Accession No. NRRL B-50972 or Accession No. NRRL B-67129 and described in International Patent Publication No. WO 2016/154297, (18.001) a composition comprising one or more fatty acids or derivatives thereof selected from unsaturated and saturated C₁₂-C₂₄ fatty acids, salts thereof, esters thereof or mixtures of any of the foregoing, wherein at least 95% of said fatty acids or derivatives thereof are in the range of C₁₄ to C₂₀ (e.g. FLiPPER by AlphaBio Pesticides or Bayer AG).

Compound (B) is most preferably selected from:

(1.002) difenoconazole, (1.018) prothioconazole, (1.020) spiroxamine, (1.021) tebuconazole, (1.055) mefentrifluconazole, (1.062) fluoxy¬tio¬conazole, (1.067) N′-(2,5-dimethyl-4-{3-[(1,1,2,2-tetrafluoro¬ethyl)sulfanyl]¬phenoxy}phenyl)-N-ethyl-N-methyl¬imido¬formamide (2.002) bixafen, (2.005) fluopyram, (2.028) inpyrfluxam, (2.038) isoflucypram, (3.020) trifloxystrobin, (3.025) fenpicoxamid, (5.003) captan, (5.010) dithianon, (5.012) folpet, (5.013) mancozeb, (5.018) propineb, (6.002) isotianil, (7.005) pyrimethanil, (13.001) fludioxonil, (13.004) proquinazid, (13.005) quinoxyfen, (15.012) fosetyl-aluminium, (15.016) metrafenone, (15.043) fluoxa¬piprolin and (15.064) (N′-[2-chloro-4-(2-fluorophenoxy)-5-methylphenyl]-N-ethyl-N-methylimidoformamide), (17.001) Bacillus subtilis, in particular strain QST713/AQ713 (available as SERENADE OPTI or SERENADE ASO from Bayer CropScience LP, US, having NRRL Accession No. B21661 and described in U.S. Pat. No. 6,060,051), (17.012) a Paenibacillus sp. strain having Accession No. NRRL B-50972 or Accession No. NRRL B-67129 and described in International Patent Publication No. WO 2016/154297, (18.001) a composition comprising one or more fatty acids or derivatives thereof selected from unsaturated and saturated C₁₂-C₂₄ fatty acids, salts thereof, esters thereof or mixtures of any of the foregoing, wherein at least 95% of said fatty acids or derivatives thereof are in the range of C₁₄ to C₂₀ (e.g. FLiPPER by AlphaBio Pesticides or Bayer AG).

Compound (B) is likewise most preferably selected from:

(1.002) difenoconazole, (1.018) prothioconazole, (1.020) spiroxamine, (1.021) tebuconazole, (1.055) mefentrifluconazole (2.002) bixafen, (2.005) fluopyram, (2.028) inpyrfluxam, (2.038) isoflucypram, (3.020) trifloxystrobin, (3.025) fenpicoxamid, (5.003) captan, (5.010) dithianon, (5.012) folpet, (5.013) mancozeb, (5.018) propineb, (6.002) isotianil, (7.005) pyrimethanil, (13.001) fludioxonil, (13.004) proquinazid, (13.005) quinoxyfen, (15.012) fosetyl-aluminium, (15.016) metrafenone and (15.064) (N′-[2-chloro-4-(2-fluorophenoxy)-5-methylphenyl]-N-ethyl-N-methylimidoformamide), (17.001) Bacillus subtilis, in particular strain QST713/AQ713 (available as SERENADE OPTI or SERENADE ASO from Bayer CropScience LP, US, having NRRL Accession No. B21661 and described in U.S. Pat. No. 6,060,051), (17.012) a Paenibacillus sp. strain having Accession No. NRRL B-50972 or Accession No. NRRL B-67129 and described in International Patent Publication No. WO 2016/154297, (18.001) a composition comprising one or more fatty acids or derivatives thereof selected from unsaturated and saturated C₁₂-C₂₄ fatty acids, salts thereof, esters thereof or mixtures of any of the foregoing, wherein at least 95% of said fatty acids or derivatives thereof are in the range of C₁₄ to C₂₀ (e.g. FLiPPER by AlphaBio Pesticides or Bayer AG).

The compound combinations according to the invention may comprise 1, 2 or even more compounds (B). Preferably, the compound combinations according to the invention comprise 1 or 2 compound(s) (B).

In case two or more compound(s) (B) are present, those compounds may be selected from different groups (1) to (18). For example, if one compound (B) is selected from group (1), the further compound(s) (B) may be selected from groups (2) to (18).

Preferred compound combinations are selected from group (G1-1) consisting of the following mixtures:

(I-052)+(1.001), (I-052)+(1.002), (I-052)+(1.003), (I-052)+(1.004), (I-052)+(1.005), (I-052)+(1.006), (I-052)+(1.007), (I-052)+(1.008), (I-052)+(1.009), (I-052)+(1.010), (I-052)+(1.011), (I-052)+(1.012), (I-052)+(1.013), (I-052)+(1.014), (I-052)+(1.015), (I-052)+(1.016), (I-052)+(1.017), (I-052)+(1.018), (I-052)+(1.019), (I-052)+(1.020), (I-052)+(1.021), (I-052)+(1.022), (I-052)+(1.023), (I-052)+(1.024), (I-052)+(1.025), (I-052)+(1.026), (I-052)+(1.027), (I-052)+(1.028), (I-052)+(1.029), (I-052)+(1.030), (I-052)+(1.031), (I-052)+(1.032), (I-052)+(1.033), (I-052)+(1.034), (I-052)+(1.035), (I-052)+(1.036), (I-052)+(1.037), (I-052)+(1.038), (I-052)+(1.039), (I-052)+(1.040), (I-052)+(1.041), (I-052)+(1.042), (I-052)+(1.043), (I-052)+(1.044), (I-052)+(1.045), (I-052)+(1.046), (I-052)+(1.047), (I-052)+(1.048), (I-052)+(1.049), (I-052)+(1.050), (I-052)+(1.051), (I-052)+(1.052), (I-052)+(1.053), (I-052)+(1.054), (I-052)+(1.055), (I-052)+(1.056), (I-052)+(1.057), (I-052)+(1.058), (I-052)+(1.059), (I-052)+(1.060), (I-052)+(1.061), (I-052)+(1.062), (I-052)+(1.063), (I-052)+(1.064), (I-052)+(1.065), (I-052)+(1.066), (I-052)+(1.067), (I-052)+(1.068), (I-052)+(1.069), (I-052)+(1.070), (I-052)+(1.071), (I-052)+(1.072), (I-052)+(1.073), (I-052)+(1.074), (I-052)+(1.075), (I-052)+(1.076), (I-052)+(1.077), (I-052)+(1.078), (I-052)+(1.079), (I-052)+(1.080), (I-052)+(1.081), (I-052)+(1.082), (I-052)+(1.083), (I-052)+(1.084), (I-052)+(1.085), (I-052)+(1.086), (I-052)+(1.087), (I-052)+(1.088), (I-052)+(1.089), (I-052)+(1.090), (I-052)+(1.091), (I-052)+(1.092), (I-052)+(2.001), (I-052)+(2.002), (I-052)+(2.003), (I-052)+(2.004), (I-052)+(2.005), (I-052)+(2.006), (I-052)+(2.007), (I-052)+(2.008), (I-052)+(2.009), (I-052)+(2.010), (I-052)+(2.011), (I-052)+(2.012), (I-052)+(2.013), (I-052)+(2.014), (I-052)+(2.015), (I-052)+(2.016), (I-052)+(2.017), (I-052)+(2.018), (I-052)+(2.019), (I-052)+(2.020), (I-052)+(2.021), (I-052)+(2.022), (I-052)+(2.023), (I-052)+(2.024), (I-052)+(2.025), (I-052)+(2.026), (I-052)+(2.027), (I-052)+(2.028), (I-052)+(2.029), (I-052)+(2.030), (I-052)+(2.031), (I-052)+(2.032), (I-052)+(2.033), (I-052)+(2.034), (I-052)+(2.035), (I-052)+(2.036), (I-052)+(2.037), (I-052)+(2.038), (I-052)+(2.039), (I-052)+(2.040), (I-052)+(2.041), (I-052)+(2.042), (I-052)+(2.043), (I-052)+(2.044), (I-052)+(2.045), (I-052)+(2.046), (I-052)+(2.047), (I-052)+(2.048), (I-052)+(2.049), (I-052)+(2.050), (I-052)+(2.051), (I-052)+(2.052), (I-052)+(2.053), (I-052)+(2.054), (I-052)+(2.055), (I-052)+(2.056), (I-052)+(2.057), (I-052)+(2.058), (I-052)+(2.059), (I-052)+(2.060), (I-052)+(3.001), (I-052)+(3.002), (I-052)+(3.003), (I-052)+(3.004), (I-052)+(3.005), (I-052)+(3.006), (I-052)+(3.007), (I-052)+(3.008), (I-052)+(3.009), (I-052)+(3.010), (I-052)+(3.011), (I-052)+(3.012), (I-052)+(3.013), (I-052)+(3.014), (I-052)+(3.015), (I-052)+(3.016), (I-052)+(3.017), (I-052)+(3.018), (I-052)+(3.019), (I-052)+(3.020), (I-052)+(3.021), (I-052)+(3.022), (I-052)+(3.023), (I-052)+(3.024), (I-052)+(3.025), (I-052)+(3.026), (I-052)+(3.027), (I-052)+(3.028), (I-052)+(3.029), (I-052)+(3.030), (I-052)+(3.031), (I-052)+(3.032), (I-052)+(4.001), (I-052)+(4.002), (I-052)+(4.003), (I-052)+(4.004), (I-052)+(4.005), (I-052)+(4.006), (I-052)+(4.007), (I-052)+(4.008), (I-052)+(4.009), (I-052)+(4.010), (I-052)+(4.011), (I-052)+(4.012), (I-052)+(4.013), (I-052)+(4.014), (I-052)+(4.015), (I-052)+(4.016), (I-052)+(4.017), (I-052)+(4.018), (I-052)+(4.019), (I-052)+(4.020), (I-052)+(4.021), (I-052)+(4.022), (I-052)+(4.023), (I-052)+(4.024), (I-052)+(4.025), (I-052)+(4.026), (I-052)+(5.001), (I-052)+(5.002), (I-052)+(5.003), (I-052)+(5.004), (I-052)+(5.005), (I-052)+(5.006), (I-052)+(5.007), (I-052)+(5.008), (I-052)+(5.009), (I-052)+(5.010), (I-052)+(5.011), (I-052)+(5.012), (I-052)+(5.013), (I-052)+(5.014), (I-052)+(5.015), (I-052)+(5.016), (I-052)+(5.017), (I-052)+(5.018), (I-052)+(5.019), (I-052)+(5.020), (I-052)+(5.021), (I-052)+(5.022), (I-052)+(5.023), (I-052)+(6.001), (I-052)+(6.002), (I-052)+(6.003), (I-052)+(6.004), (I-052)+(7.001), (I-052)+(7.002), (I-052)+(7.003), (I-052)+(7.004), (I-052)+(7.005), (I-052)+(7.006), (I-052)+(8.001), (I-052)+(9.001), (I-052)+(9.002), (I-052)+(9.003), (I-052)+(9.004), (I-052)+(9.005), (I-052)+(9.006), (I-052)+(9.007), (I-052)+(9.008), (I-052)+(9.009), (I-052)+(10.001), (I-052)+(10.002), (I-052)+(10.003), (I-052)+(11.001), (I-052)+(11.002), (I-052)+(12.001), (I-052)+(12.002), (I-052)+(12.003), (I-052)+(12.004), (I-052)+(13.001), (I-052)+(13.002), (I-052)+(13.003), (I-052)+(13.004), (I-052)+(13.005), (I-052)+(13.006), (I-052)+(14.001), (I-052)+(14.002), (I-052)+(15.001), (I-052)+(15.002), (I-052)+(15.003), (I-052)+(15.004), (I-052)+(15.005), (I-052)+(15.006), (I-052)+(15.007), (I-052)+(15.008), (I-052)+(15.009), (I-052)+(15.010), (I-052)+(15.011), (I-052)+(15.012), (I-052)+(15.013), (I-052)+(15.014), (I-052)+(15.015), (I-052)+(15.016), (I-052)+(15.017), (I-052)+(15.018), (I-052)+(15.019), (I-052)+(15.020), (I-052)+(15.021), (I-052)+(15.022), (I-052)+(15.023), (I-052)+(15.024), (I-052)+(15.025), (I-052)+(15.026), (I-052)+(15.027), (I-052)+(15.028), (I-052)+(15.029), (I-052)+(15.030), (I-052)+(15.031), (I-052)+(15.032), (I-052)+(15.033), (I-052)+(15.034), (I-052)+(15.035), (I-052)+(15.036), (I-052)+(15.037), (I-052)+(15.038), (I-052)+(15.039), (I-052)+(15.040), (I-052)+(15.041), (I-052)+(15.042), (I-052)+(15.043), (I-052)+(15.044), (I-052)+(15.045), (I-052)+(15.046), (I-052)+(15.047), (I-052)+(15.048), (I-052)+(15.049), (I-052)+(15.050), (I-052)+(15.051), (I-052)+(15.052), (I-052)+(15.053), (I-052)+(15.054), (I-052)+(15.055), (I-052)+(15.056), (I-052)+(15.057), (I-052)+(15.058), (I-052)+(15.059), (I-052)+(15.060), (I-052)+(15.061), (I-052)+(15.062), (I-052)+(15.063), (I-052)+(15.064), (I-052)+(15.065), (I-052)+(15.066), (I-052)+(15.067), (I-052)+(15.068), (I-052)+(15.069), (I-052)+(15.070), (I-052)+(15.071), (I-052)+(15.072), (I-052)+(15.073), (I-052)+(15.074), (I-052)+(15.075), (I-052)+(15.076), (I-052)+(15.077), (I-052)+(15.078), (I-052)+(15.079), (I-052)+(15.080), (I-052)+(15.081), (I-052)+(15.082), (I-052)+(15.083), (I-052)+(15.084), (I-052)+(15.085), (I-052)+(15.086), (I-052)+(15.087), (I-052)+(15.088), (I-052)+(15.089), (I-052)+(15.090), (I-052)+(15.091), (I-052)+(15.092), (I-052)+(15.093), (I-052)+(15.094), (I-052)+(15.095), (I-052)+(15.096), (I-052)+(15.097), (I-052)+(15.098), (I-052)+(15.099), (I-052)+(15.100), (I-052)+(15.101), (I-052)+(15.102), (I-052)+(15.103), (I-052)+(15.104), (I-052)+(15.105), (I-052)+(15.106), (I-052)+(15.107), (I-052)+(15.108), (I-052)+(15.109), (I-052)+(15.110), (I-052)+(15.111), (I-052)+(15.112), (I-052)+(15.113), (I-052)+(15.114), (I-052)+(15.115), (I-052)+(15.116), (I-052)+(15.117), (I-052)+(15.118), (I-052)+(15.119), (I-052)+(15.120), (I-052)+(15.121), (I-052)+(15.122), (I-052)+(15.123), (I-052)+(15.124), (I-052)+(15.125), (I-052)+(15.126), (I-052)+(15.127), (I-052)+(15.128), (I-052)+(16.001), (I-052)+(16.002), (I-052)+(16.003), (I-052)+(16.004), (I-052)+(16.005), (I-052)+(16.006), (I-052)+(16.007), (I-052)+(16.008), (I-052)+(17.001), (I-052)+(17.002), (I-052)+(17.003), (I-052)+(17.004), (I-052)+(17.005), (I-052)+(17.006), (I-052)+(17.007), (I-052)+(17.008), (I-052)+(17.009), (I-052)+(17.010), (I-052)+(17.011), (I-052)+(17.012) and (I-052)+(18.001).

Preferred compound combinations are selected from group (G1) consisting of the following mixtures:

(I-052)+(1.001), (I-052)+(1.002), (I-052)+(1.003), (I-052)+(1.004), (I-052)+(1.005), (I-052)+(1.006), (I-052)+(1.007), (I-052)+(1.008), (I-052)+(1.009), (I-052)+(1.010), (I-052)+(1.011), (I-052)+(1.012), (I-052)+(1.013), (I-052)+(1.014), (I-052)+(1.015), (I-052)+(1.016), (I-052)+(1.017), (I-052)+(1.018), (I-052)+(1.019), (I-052)+(1.020), (I-052)+(1.021), (I-052)+(1.022), (I-052)+(1.023), (I-052)+(1.024), (I-052)+(1.025), (I-052)+(1.026), (I-052)+(1.027), (I-052)+(1.028), (I-052)+(1.029), (I-052)+(1.030), (I-052)+(1.031), (I-052)+(1.032), (I-052)+(1.033), (I-052)+(1.034), (I-052)+(1.035), (I-052)+(1.036), (I-052)+(1.037), (I-052)+(1.038), (I-052)+(1.039), (I-052)+(1.040), (I-052)+(1.041), (I-052)+(1.042), (I-052)+(1.043), (I-052)+(1.044), (I-052)+(1.045), (I-052)+(1.046), (I-052)+(1.047), (I-052)+(1.048), (I-052)+(1.049), (I-052)+(1.050), (I-052)+(1.051), (I-052)+(1.052), (I-052)+(1.053), (I-052)+(1.054), (I-052)+(1.055), (I-052)+(1.056), (I-052)+(1.057), (I-052)+(1.058), (I-052)+(1.059), (I-052)+(1.060), (I-052)+(1.061), (I-052)+(1.062), (I-052)+(1.063), (I-052)+(1.064), (I-052)+(1.065), (I-052)+(1.066), (I-052)+(1.067), (I-052)+(1.068), (I-052)+(1.069), (I-052)+(1.070), (I-052)+(1.071), (I-052)+(1.072), (I-052)+(1.073), (I-052)+(1.074), (I-052)+(1.075), (I-052)+(1.076), (I-052)+(1.077), (I-052)+(1.078), (I-052)+(1.079), (I-052)+(1.080), (I-052)+(1.081), (I-052)+(1.082), (I-052)+(1.083), (I-052)+(1.084), (I-052)+(1.085), (I-052)+(1.086), (I-052)+(1.087), (I-052)+(1.088), (I-052)+(1.089), (I-052)+(1.090), (I-052)+(1.091), (I-052)+(1.092), (I-052)+(2.001), (I-052)+(2.002), (I-052)+(2.003), (I-052)+(2.004), (I-052)+(2.005), (I-052)+(2.006), (I-052)+(2.007), (I-052)+(2.008), (I-052)+(2.009), (I-052)+(2.010), (I-052)+(2.011), (I-052)+(2.012), (I-052)+(2.013), (I-052)+(2.014), (I-052)+(2.015), (I-052)+(2.016), (I-052)+(2.017), (I-052)+(2.018), (I-052)+(2.019), (I-052)+(2.020), (I-052)+(2.021), (I-052)+(2.022), (I-052)+(2.023), (I-052)+(2.024), (I-052)+(2.025), (I-052)+(2.026), (I-052)+(2.027), (I-052)+(2.028), (I-052)+(2.029), (I-052)+(2.030), (I-052)+(2.031), (I-052)+(2.032), (I-052)+(2.033), (I-052)+(2.034), (I-052)+(2.035), (I-052)+(2.036), (I-052)+(2.037), (I-052)+(2.038), (I-052)+(2.039), (I-052)+(2.040), (I-052)+(2.041), (I-052)+(2.042), (I-052)+(2.043), (I-052)+(2.044), (I-052)+(2.045), (I-052)+(2.046), (I-052)+(2.047), (I-052)+(2.048), (I-052)+(2.049), (I-052)+(2.050), (I-052)+(2.051), (I-052)+(2.052), (I-052)+(2.053), (I-052)+(2.054), (I-052)+(2.055), (I-052)+(2.056), (I-052)+(2.057), (I-052)+(2.058), (I-052)+(2.059), (I-052)+(3.001), (I-052)+(3.002), (I-052)+(3.003), (I-052)+(3.004), (I-052)+(3.005), (I-052)+(3.006), (I-052)+(3.007), (I-052)+(3.008), (I-052)+(3.009), (I-052)+(3.010), (I-052)+(3.011), (I-052)+(3.012), (I-052)+(3.013), (I-052)+(3.014), (I-052)+(3.015), (I-052)+(3.016), (I-052)+(3.017), (I-052)+(3.018), (I-052)+(3.019), (I-052)+(3.020), (I-052)+(3.021), (I-052)+(3.022), (I-052)+(3.023), (I-052)+(3.024), (I-052)+(3.025), (I-052)+(3.026), (I-052)+(3.027), (I-052)+(3.028), (I-052)+(3.029), (I-052)+(3.030), (I-052)+(3.031), (I-052)+(4.001), (I-052)+(4.002), (I-052)+(4.003), (I-052)+(4.004), (I-052)+(4.005), (I-052)+(4.006), (I-052)+(4.007), (I-052)+(4.008), (I-052)+(4.009), (I-052)+(4.010), (I-052)+(4.011), (I-052)+(4.012), (I-052)+(4.013), (I-052)+(4.014), (I-052)+(4.015), (I-052)+(4.016), (I-052)+(4.017), (I-052)+(4.018), (I-052)+(4.019), (I-052)+(4.020), (I-052)+(4.021), (I-052)+(4.022), (I-052)+(4.023), (I-052)+(4.024), (I-052)+(4.025), (I-052)+(4.026), (I-052)+(5.001), (I-052)+(5.002), (I-052)+(5.003), (I-052)+(5.004), (I-052)+(5.005), (I-052)+(5.006), (I-052)+(5.007), (I-052)+(5.008), (I-052)+(5.009), (I-052)+(5.010), (I-052)+(5.011), (I-052)+(5.012), (I-052)+(5.013), (I-052)+(5.014), (I-052)+(5.015), (I-052)+(5.016), (I-052)+(5.017), (I-052)+(5.018), (I-052)+(5.019), (I-052)+(5.020), (I-052)+(5.021), (I-052)+(5.022), (I-052)+(5.023), (I-052)+(6.001), (I-052)+(6.002), (I-052)+(6.003), (I-052)+(6.004), (I-052)+(7.001), (I-052)+(7.002), (I-052)+(7.003), (I-052)+(7.004), (I-052)+(7.005), (I-052)+(7.006), (I-052)+(8.001), (I-052)+(9.001), (I-052)+(9.002), (I-052)+(9.003), (I-052)+(9.004), (I-052)+(9.005), (I-052)+(9.006), (I-052)+(9.007), (I-052)+(9.008), (I-052)+(9.009), (I-052)+(10.001), (I-052)+(10.002), (I-052)+(10.003), (I-052)+(11.001), (I-052)+(11.002), (I-052)+(12.001), (I-052)+(12.002), (I-052)+(12.003), (I-052)+(12.004), (I-052)+(13.001), (I-052)+(13.002), (I-052)+(13.003), (I-052)+(13.004), (I-052)+(13.005), (I-052)+(13.006), (I-052)+(14.001), (I-052)+(14.002), (I-052)+(15.001), (I-052)+(15.002), (I-052)+(15.003), (I-052)+(15.004), (I-052)+(15.005), (I-052)+(15.006), (I-052)+(15.007), (I-052)+(15.008), (I-052)+(15.009), (I-052)+(15.010), (I-052)+(15.011), (I-052)+(15.012), (I-052)+(15.013), (I-052)+(15.014), (I-052)+(15.015), (I-052)+(15.016), (I-052)+(15.017), (I-052)+(15.018), (I-052)+(15.019), (I-052)+(15.020), (I-052)+(15.021), (I-052)+(15.022), (I-052)+(15.023), (I-052)+(15.024), (I-052)+(15.025), (I-052)+(15.026), (I-052)+(15.027), (I-052)+(15.028), (I-052)+(15.029), (I-052)+(15.030), (I-052)+(15.031), (I-052)+(15.032), (I-052)+(15.033), (I-052)+(15.034), (I-052)+(15.035), (I-052)+(15.036), (I-052)+(15.037), (I-052)+(15.038), (I-052)+(15.039), (I-052)+(15.040), (I-052)+(15.041), (I-052)+(15.042), (I-052)+(15.043), (I-052)+(15.044), (I-052)+(15.045), (I-052)+(15.046), (I-052)+(15.047), (I-052)+(15.048), (I-052)+(15.049), (I-052)+(15.050), (I-052)+(15.051), (I-052)+(15.052), (I-052)+(15.053), (I-052)+(15.054), (I-052)+(15.055), (I-052)+(15.056), (I-052)+(15.057), (I-052)+(15.058), (I-052)+(15.059), (I-052)+(15.060), (I-052)+(15.061), (I-052)+(15.062), (I-052)+(15.063), (I-052)+(15.064), (I-052)+(15.065), (I-052)+(15.066), (I-052)+(15.067), (I-052)+(15.068), (I-052)+(15.069), (I-052)+(15.070), (I-052)+(15.071), (I-052)+(15.072), (I-052)+(15.073), (I-052)+(15.074), (I-052)+(15.075), (I-052)+(15.076), (I-052)+(15.077), (I-052)+(15.078), (I-052)+(15.079), (I-052)+(15.080), (I-052)+(15.081), (I-052)+(15.082), (I-052)+(15.083), (I-052)+(15.084), (I-052)+(15.085), (I-052)+(15.086), (I-052)+(15.087), (I-052)+(15.088), (I-052)+(15.089), (I-052)+(15.090), (I-052)+(15.091), (I-052)+(15.092), (I-052)+(15.093), (I-052)+(15.094), (I-052)+(15.095), (I-052)+(15.096), (I-052)+(15.097), (I-052)+(15.098), (I-052)+(15.099), (I-052)+(15.100), (I-052)+(15.101), (I-052)+(15.102), (I-052)+(15.103), (I-052)+(15.104), (I-052)+(15.105), (I-052)+(15.106), (I-052)+(15.107), (I-052)+(15.108), (I-052)+(15.109), (I-052)+(15.110), (I-052)+(15.111), (I-052)+(15.112), (I-052)+(15.113), (I-052)+(15.114), (I-052)+(15.115), (I-052)+(15.116), (I-052)+(15.117), (I-052)+(15.118), (I-052)+(15.119), (I-052)+(15.120), (I-052)+(15.121), (I-052)+(15.122), (I-052)+(15.123), (I-052)+(15.124), (I-052)+(15.125), (I-052)+(15.126), (I-052)+(15.127), (I-052)+(16.001), (I-052)+(16.002), (I-052)+(16.003), (I-052)+(16.004), (I-052)+(16.005), (I-052)+(16.006), (I-052)+(16.007), (I-052)+(16.008), (I-052)+(17.001), (I-052)+(17.002), (I-052)+(17.003), (I-052)+(17.004), (I-052)+(17.005), (I-052)+(17.006), (I-052)+(17.007), (I-052)+(17.008), (I-052)+(17.009), (I-052)+(17.010), (I-052)+(17.011), (I-052)+(17.012) and (I-052)+(18.001).

Also preferred compound combinations are selected from group (G2-1) consisting of the following mixtures:

(I-130)+(1.001), (I-130)+(1.002), (I-130)+(1.003), (I-130)+(1.004), (I-130)+(1.005), (I-130)+(1.006), (I-130)+(1.007), (I-130)+(1.008), (I-130)+(1.009), (I-130)+(1.010), (I-130)+(1.011), (I-130)+(1.012), (I-130)+(1.013), (I-130)+(1.014), (I-130)+(1.015), (I-130)+(1.016), (I-130)+(1.017), (I-130)+(1.018), (I-130)+(1.019), (I-130)+(1.020), (I-130)+(1.021), (I-130)+(1.022), (I-130)+(1.023), (I-130)+(1.024), (I-130)+(1.025), (I-130)+(1.026), (I-130)+(1.027), (I-130)+(1.028), (I-130)+(1.029), (I-130)+(1.030), (I-130)+(1.031), (I-130)+(1.032), (I-130)+(1.033), (I-130)+(1.034), (I-130)+(1.035), (I-130)+(1.036), (I-130)+(1.037), (I-130)+(1.038), (I-130)+(1.039), (I-130)+(1.040), (I-130)+(1.041), (I-130)+(1.042), (I-130)+(1.043), (I-130)+(1.044), (I-130)+(1.045), (I-130)+(1.046), (I-130)+(1.047), (I-130)+(1.048), (I-130)+(1.049), (I-130)+(1.050), (I-130)+(1.051), (I-130)+(1.052), (I-130)+(1.053), (I-130)+(1.054), (I-130)+(1.055), (I-130)+(1.056), (I-130)+(1.057), (I-130)+(1.058), (I-130)+(1.059), (I-130)+(1.060), (I-130)+(1.061), (I-130)+(1.062), (I-130)+(1.063), (I-130)+(1.064), (I-130)+(1.065), (I-130)+(1.066), (I-130)+(1.067), (I-130)+(1.068), (I-130)+(1.069), (I-130)+(1.070), (I-130)+(1.071), (I-130)+(1.072), (I-130)+(1.073), (I-130)+(1.074), (I-130)+(1.075), (I-130)+(1.076), (I-130)+(1.077), (I-130)+(1.078), (I-130)+(1.079), (I-130)+(1.080), (I-130)+(1.081), (I-130)+(1.082), (I-130)+(1.083), (I-130)+(1.084), (I-130)+(1.085), (I-130)+(1.086), (I-130)+(1.087), (I-130)+(1.088), (I-130)+(1.089), (I-130)+(1.090), (I-130)+(1.091), (I-130)+(1.092), (I-130)+(2.001), (I-130)+(2.002), (I-130)+(2.003), (I-130)+(2.004), (I-130)+(2.005), (I-130)+(2.006), (I-130)+(2.007), (I-130)+(2.008), (I-130)+(2.009), (I-130)+(2.010), (I-130)+(2.011), (I-130)+(2.012), (I-130)+(2.013), (I-130)+(2.014), (I-130)+(2.015), (I-130)+(2.016), (I-130)+(2.017), (I-130)+(2.018), (I-130)+(2.019), (I-130)+(2.020), (I-130)+(2.021), (I-130)+(2.022), (I-130)+(2.023), (I-130)+(2.024), (I-130)+(2.025), (I-130)+(2.026), (I-130)+(2.027), (I-130)+(2.028), (I-130)+(2.029), (I-130)+(2.030), (I-130)+(2.031), (I-130)+(2.032), (I-130)+(2.033), (I-130)+(2.034), (I-130)+(2.035), (I-130)+(2.036), (I-130)+(2.037), (I-130)+(2.038), (I-130)+(2.039), (I-130)+(2.040), (I-130)+(2.041), (I-130)+(2.042), (I-130)+(2.043), (I-130)+(2.044), (I-130)+(2.045), (I-130)+(2.046), (I-130)+(2.047), (I-130)+(2.048), (I-130)+(2.049), (I-130)+(2.050), (I-130)+(2.051), (I-130)+(2.052), (I-130)+(2.053), (I-130)+(2.054), (I-130)+(2.055), (I-130)+(2.056), (I-130)+(2.057), (I-130)+(2.058), (I-130)+(2.059), (I-130)+(2.060), (I-130)+(3.001), (I-130)+(3.002), (I-130)+(3.003), (I-130)+(3.004), (I-130)+(3.005), (I-130)+(3.006), (I-130)+(3.007), (I-130)+(3.008), (I-130)+(3.009), (I-130)+(3.010), (I-130)+(3.011), (I-130)+(3.012), (I-130)+(3.013), (I-130)+(3.014), (I-130)+(3.015), (I-130)+(3.016), (I-130)+(3.017), (I-130)+(3.018), (I-130)+(3.019), (I-130)+(3.020), (I-130)+(3.021), (I-130)+(3.022), (I-130)+(3.023), (I-130)+(3.024), (I-130)+(3.025), (I-130)+(3.026), (I-130)+(3.027), (I-130)+(3.028), (I-130)+(3.029), (I-130)+(3.030), (I-130)+(3.031), (I-130)+(3.032), (I-130)+(4.001), (I-130)+(4.002), (I-130)+(4.003), (I-130)+(4.004), (I-130)+(4.005), (I-130)+(4.006), (I-130)+(4.007), (I-130)+(4.008), (I-130)+(4.009), (I-130)+(4.010), (I-130)+(4.011), (I-130)+(4.012), (I-130)+(4.013), (I-130)+(4.014), (I-130)+(4.015), (I-130)+(4.016), (I-130)+(4.017), (I-130)+(4.018), (I-130)+(4.019), (I-130)+(4.020), (I-130)+(4.021), (I-130)+(4.022), (I-130)+(4.023), (I-130)+(4.024), (I-130)+(4.025), (I-130)+(4.026), (I-130)+(5.001), (I-130)+(5.002), (I-130)+(5.003), (I-130)+(5.004), (I-130)+(5.005), (I-130)+(5.006), (I-130)+(5.007), (I-130)+(5.008), (I-130)+(5.009), (I-130)+(5.010), (I-130)+(5.011), (I-130)+(5.012), (I-130)+(5.013), (I-130)+(5.014), (I-130)+(5.015), (I-130)+(5.016), (I-130)+(5.017), (I-130)+(5.018), (I-130)+(5.019), (I-130)+(5.020), (I-130)+(5.021), (I-130)+(5.022), (I-130)+(5.023), (I-130)+(6.001), (I-130)+(6.002), (I-130)+(6.003), (I-130)+(6.004), (I-130)+(7.001), (I-130)+(7.002), (I-130)+(7.003), (I-130)+(7.004), (I-130)+(7.005), (I-130)+(7.006), (I-130)+(8.001), (I-130)+(9.001), (I-130)+(9.002), (I-130)+(9.003), (I-130)+(9.004), (I-130)+(9.005), (I-130)+(9.006), (I-130)+(9.007), (I-130)+(9.008), (I-130)+(9.009), (I-130)+(10.001), (I-130)+(10.002), (I-130)+(10.003), (I-130)+(11.001), (I-130)+(11.002), (I-130)+(12.001), (I-130)+(12.002), (I-130)+(12.003), (I-130)+(12.004), (I-130)+(13.001), (I-130)+(13.002), (I-130)+(13.003), (I-130)+(13.004), (I-130)+(13.005), (I-130)+(13.006), (I-130)+(14.001), (I-130)+(14.002), (I-130)+(15.001), (I-130)+(15.002), (I-130)+(15.003), (I-130)+(15.004), (I-130)+(15.005), (I-130)+(15.006), (I-130)+(15.007), (I-130)+(15.008), (I-130)+(15.009), (I-130)+(15.010), (I-130)+(15.011), (I-130)+(15.012), (I-130)+(15.013), (I-130)+(15.014), (I-130)+(15.015), (I-130)+(15.016), (I-130)+(15.017), (I-130)+(15.018), (I-130)+(15.019), (I-130)+(15.020), (I-130)+(15.021), (I-130)+(15.022), (I-130)+(15.023), (I-130)+(15.024), (I-130)+(15.025), (I-130)+(15.026), (I-130)+(15.027), (I-130)+(15.028), (I-130)+(15.029), (I-130)+(15.030), (I-130)+(15.031), (I-130)+(15.032), (I-130)+(15.033), (I-130)+(15.034), (I-130)+(15.035), (I-130)+(15.036), (I-130)+(15.037), (I-130)+(15.038), (I-130)+(15.039), (I-130)+(15.040), (I-130)+(15.041), (I-130)+(15.042), (I-130)+(15.043), (I-130)+(15.044), (I-130)+(15.045), (I-130)+(15.046), (I-130)+(15.047), (I-130)+(15.048), (I-130)+(15.049), (I-130)+(15.050), (I-130)+(15.051), (I-130)+(15.052), (I-130)+(15.053), (I-130)+(15.054), (I-130)+(15.055), (I-130)+(15.056), (I-130)+(15.057), (I-130)+(15.058), (I-130)+(15.059), (I-130)+(15.060), (I-130)+(15.061), (I-130)+(15.062), (I-130)+(15.063), (I-130)+(15.064), (I-130)+(15.065), (I-130)+(15.066), (I-130)+(15.067), (I-130)+(15.068), (I-130)+(15.069), (I-130)+(15.070), (I-130)+(15.071), (I-130)+(15.072), (I-130)+(15.073), (I-130)+(15.074), (I-130)+(15.075), (I-130)+(15.076), (I-130)+(15.077), (I-130)+(15.078), (I-130)+(15.079), (I-130)+(15.080), (I-130)+(15.081), (I-130)+(15.082), (I-130)+(15.083), (I-130)+(15.084), (I-130)+(15.085), (I-130)+(15.086), (I-130)+(15.087), (I-130)+(15.088), (I-130)+(15.089), (I-130)+(15.090), (I-130)+(15.091), (I-130)+(15.092), (I-130)+(15.093), (I-130)+(15.094), (I-130)+(15.095), (I-130)+(15.096), (I-130)+(15.097), (I-130)+(15.098), (I-130)+(15.099), (I-130)+(15.100), (I-130)+(15.101), (I-130)+(15.102), (I-130)+(15.103), (I-130)+(15.104), (I-130)+(15.105), (I-130)+(15.106), (I-130)+(15.107), (I-130)+(15.108), (I-130)+(15.109), (I-130)+(15.110), (I-130)+(15.111), (I-130)+(15.112), (I-130)+(15.113), (I-130)+(15.114), (I-130)+(15.115), (I-130)+(15.116), (I-130)+(15.117), (I-130)+(15.118), (I-130)+(15.119), (I-130)+(15.120), (I-130)+(15.121), (I-130)+(15.122), (I-130)+(15.123), (I-130)+(15.124), (I-130)+(15.125), (I-130)+(15.126), (I-130)+(15.127), (I-130)+(15.128), (I-130)+(16.001), (I-130)+(16.002), (I-130)+(16.003), (I-130)+(16.004), (I-130)+(16.005), (I-130)+(16.006), (I-130)+(16.007), (I-130)+(16.008), (I-130)+(17.001), (I-130)+(17.002), (I-130)+(17.003), (I-130)+(17.004), (I-130)+(17.005), (I-130)+(17.006), (I-130)+(17.007), (I-130)+(17.008), (I-130)+(17.009), (I-130)+(17.010), (I-130)+(17.011), (I-130)+(17.012) and (I-130)+(18.001).

Also preferred compound combinations are selected from group (G2) consisting of the following mixtures:

(I-130)+(1.001), (I-130)+(1.002), (I-130)+(1.003), (I-130)+(1.004), (I-130)+(1.005), (I-130)+(1.006), (I-130)+(1.007), (I-130)+(1.008), (I-130)+(1.009), (I-130)+(1.010), (I-130)+(1.011), (I-130)+(1.012), (I-130)+(1.013), (I-130)+(1.014), (I-130)+(1.015), (I-130)+(1.016), (I-130)+(1.017), (I-130)+(1.018), (I-130)+(1.019), (I-130)+(1.020), (I-130)+(1.021), (I-130)+(1.022), (I-130)+(1.023), (I-130)+(1.024), (I-130)+(1.025), (I-130)+(1.026), (I-130)+(1.027), (I-130)+(1.028), (I-130)+(1.029), (I-130)+(1.030), (I-130)+(1.031), (I-130)+(1.032), (I-130)+(1.033), (I-130)+(1.034), (I-130)+(1.035), (I-130)+(1.036), (I-130)+(1.037), (I-130)+(1.038), (I-130)+(1.039), (I-130)+(1.040), (I-130)+(1.041), (I-130)+(1.042), (I-130)+(1.043), (I-130)+(1.044), (I-130)+(1.045), (I-130)+(1.046), (I-130)+(1.047), (I-130)+(1.048), (I-130)+(1.049), (I-130)+(1.050), (I-130)+(1.051), (I-130)+(1.052), (I-130)+(1.053), (I-130)+(1.054), (I-130)+(1.055), (I-130)+(1.056), (I-130)+(1.057), (I-130)+(1.058), (I-130)+(1.059), (I-130)+(1.060), (I-130)+(1.061), (I-130)+(1.062), (I-130)+(1.063), (I-130)+(1.064), (I-130)+(1.065), (I-130)+(1.066), (I-130)+(1.067), (I-130)+(1.068), (I-130)+(1.069), (I-130)+(1.070), (I-130)+(1.071), (I-130)+(1.072), (I-130)+(1.073), (I-130)+(1.074), (I-130)+(1.075), (I-130)+(1.076), (I-130)+(1.077), (I-130)+(1.078), (I-130)+(1.079), (I-130)+(1.080), (I-130)+(1.081), (I-130)+(1.082), (I-130)+(1.083), (I-130)+(1.084), (I-130)+(1.085), (I-130)+(1.086), (I-130)+(1.087), (I-130)+(1.088), (I-130)+(1.089), (I-130)+(1.090), (I-130)+(1.091), (I-130)+(1.092), (I-130)+(2.001), (I-130)+(2.002), (I-130)+(2.003), (I-130)+(2.004), (I-130)+(2.005), (I-130)+(2.006), (I-130)+(2.007), (I-130)+(2.008), (I-130)+(2.009), (I-130)+(2.010), (I-130)+(2.011), (I-130)+(2.012), (I-130)+(2.013), (I-130)+(2.014), (I-130)+(2.015), (I-130)+(2.016), (I-130)+(2.017), (I-130)+(2.018), (I-130)+(2.019), (I-130)+(2.020), (I-130)+(2.021), (I-130)+(2.022), (I-130)+(2.023), (I-130)+(2.024), (I-130)+(2.025), (I-130)+(2.026), (I-130)+(2.027), (I-130)+(2.028), (I-130)+(2.029), (I-130)+(2.030), (I-130)+(2.031), (I-130)+(2.032), (I-130)+(2.033), (I-130)+(2.034), (I-130)+(2.035), (I-130)+(2.036), (I-130)+(2.037), (I-130)+(2.038), (I-130)+(2.039), (I-130)+(2.040), (I-130)+(2.041), (I-130)+(2.042), (I-130)+(2.043), (I-130)+(2.044), (I-130)+(2.045), (I-130)+(2.046), (I-130)+(2.047), (I-130)+(2.048), (I-130)+(2.049), (I-130)+(2.050), (I-130)+(2.051), (I-130)+(2.052), (I-130)+(2.053), (I-130)+(2.054), (I-130)+(2.055), (I-130)+(2.056), (I-130)+(2.057), (I-130)+(2.058), (I-130)+(2.059), (I-130)+(3.001), (I-130)+(3.002), (I-130)+(3.003), (I-130)+(3.004), (I-130)+(3.005), (I-130)+(3.006), (I-130)+(3.007), (I-130)+(3.008), (I-130)+(3.009), (I-130)+(3.010), (I-130)+(3.011), (I-130)+(3.012), (I-130)+(3.013), (I-130)+(3.014), (I-130)+(3.015), (I-130)+(3.016), (I-130)+(3.017), (I-130)+(3.018), (I-130)+(3.019), (I-130)+(3.020), (I-130)+(3.021), (I-130)+(3.022), (I-130)+(3.023), (I-130)+(3.024), (I-130)+(3.025), (I-130)+(3.026), (I-130)+(3.027), (I-130)+(3.028), (I-130)+(3.029), (I-130)+(3.030), (I-130)+(3.031), (I-130)+(4.001), (I-130)+(4.002), (I-130)+(4.003), (I-130)+(4.004), (I-130)+(4.005), (I-130)+(4.006), (I-130)+(4.007), (I-130)+(4.008), (I-130)+(4.009), (I-130)+(4.010), (I-130)+(4.011), (I-130)+(4.012), (I-130)+(4.013), (I-130)+(4.014), (I-130)+(4.015), (I-130)+(4.016), (I-130)+(4.017), (I-130)+(4.018), (I-130)+(4.019), (I-130)+(4.020), (I-130)+(4.021), (I-130)+(4.022), (I-130)+(4.023), (I-130)+(4.024), (I-130)+(4.025), (I-130)+(4.026), (I-130)+(5.001), (I-130)+(5.002), (I-130)+(5.003), (I-130)+(5.004), (I-130)+(5.005), (I-130)+(5.006), (I-130)+(5.007), (I-130)+(5.008), (I-130)+(5.009), (I-130)+(5.010), (I-130)+(5.011), (I-130)+(5.012), (I-130)+(5.013), (I-130)+(5.014), (I-130)+(5.015), (I-130)+(5.016), (I-130)+(5.017), (I-130)+(5.018), (I-130)+(5.019), (I-130)+(5.020), (I-130)+(5.021), (I-130)+(5.022), (I-130)+(5.023), (I-130)+(6.001), (I-130)+(6.002), (I-130)+(6.003), (I-130)+(6.004), (I-130)+(7.001), (I-130)+(7.002), (I-130)+(7.003), (I-130)+(7.004), (I-130)+(7.005), (I-130)+(7.006), (I-130)+(8.001), (I-130)+(9.001), (I-130)+(9.002), (I-130)+(9.003), (I-130)+(9.004), (I-130)+(9.005), (I-130)+(9.006), (I-130)+(9.007), (I-130)+(9.008), (I-130)+(9.009), (I-130)+(10.001), (I-130)+(10.002), (I-130)+(10.003), (I-130)+(11.001), (I-130)+(11.002), (I-130)+(12.001), (I-130)+(12.002), (I-130)+(12.003), (I-130)+(12.004), (I-130)+(13.001), (I-130)+(13.002), (I-130)+(13.003), (I-130)+(13.004), (I-130)+(13.005), (I-130)+(13.006), (I-130)+(14.001), (I-130)+(14.002), (I-130)+(15.001), (I-130)+(15.002), (I-130)+(15.003), (I-130)+(15.004), (I-130)+(15.005), (I-130)+(15.006), (I-130)+(15.007), (I-130)+(15.008), (I-130)+(15.009), (I-130)+(15.010), (I-130)+(15.011), (I-130)+(15.012), (I-130)+(15.013), (I-130)+(15.014), (I-130)+(15.015), (I-130)+(15.016), (I-130)+(15.017), (I-130)+(15.018), (I-130)+(15.019), (I-130)+(15.020), (I-130)+(15.021), (I-130)+(15.022), (I-130)+(15.023), (I-130)+(15.024), (I-130)+(15.025), (I-130)+(15.026), (I-130)+(15.027), (I-130)+(15.028), (I-130)+(15.029), (I-130)+(15.030), (I-130)+(15.031), (I-130)+(15.032), (I-130)+(15.033), (I-130)+(15.034), (I-130)+(15.035), (I-130)+(15.036), (I-130)+(15.037), (I-130)+(15.038), (I-130)+(15.039), (I-130)+(15.040), (I-130)+(15.041), (I-130)+(15.042), (I-130)+(15.043), (I-130)+(15.044), (I-130)+(15.045), (I-130)+(15.046), (I-130)+(15.047), (I-130)+(15.048), (I-130)+(15.049), (I-130)+(15.050), (I-130)+(15.051), (I-130)+(15.052), (I-130)+(15.053), (I-130)+(15.054), (I-130)+(15.055), (I-130)+(15.056), (I-130)+(15.057), (I-130)+(15.058), (I-130)+(15.059), (I-130)+(15.060), (I-130)+(15.061), (I-130)+(15.062), (I-130)+(15.063), (I-130)+(15.064), (I-130)+(15.065), (I-130)+(15.066), (I-130)+(15.067), (I-130)+(15.068), (I-130)+(15.069), (I-130)+(15.070), (I-130)+(15.071), (I-130)+(15.072), (I-130)+(15.073), (I-130)+(15.074), (I-130)+(15.075), (I-130)+(15.076), (I-130)+(15.077), (I-130)+(15.078), (I-130)+(15.079), (I-130)+(15.080), (I-130)+(15.081), (I-130)+(15.082), (I-130)+(15.083), (I-130)+(15.084), (I-130)+(15.085), (I-130)+(15.086), (I-130)+(15.087), (I-130)+(15.088), (I-130)+(15.089), (I-130)+(15.090), (I-130)+(15.091), (I-130)+(15.092), (I-130)+(15.093), (I-130)+(15.094), (I-130)+(15.095), (I-130)+(15.096), (I-130)+(15.097), (I-130)+(15.098), (I-130)+(15.099), (I-130)+(15.100), (I-130)+(15.101), (I-130)+(15.102), (I-130)+(15.103), (I-130)+(15.104), (I-130)+(15.105), (I-130)+(15.106), (I-130)+(15.107), (I-130)+(15.108), (I-130)+(15.109), (I-130)+(15.110), (I-130)+(15.111), (I-130)+(15.112), (I-130)+(15.113), (I-130)+(15.114), (I-130)+(15.115), (I-130)+(15.116), (I-130)+(15.117), (I-130)+(15.118), (I-130)+(15.119), (I-130)+(15.120), (I-130)+(15.121), (I-130)+(15.122), (I-130)+(15.123), (I-130)+(15.124), (I-130)+(15.125), (I-130)+(15.126), (I-130)+(15.127), (I-130)+(16.001), (I-130)+(16.002), (I-130)+(16.003), (I-130)+(16.004), (I-130)+(16.005), (I-130)+(16.006), (I-130)+(16.007), (I-130)+(16.008), (I-130)+(17.001), (I-130)+(17.002), (I-130)+(17.003), (I-130)+(17.004), (I-130)+(17.005), (I-130)+(17.006), (I-130)+(17.007), (I-130)+(17.008), (I-130)+(17.009), (I-130)+(17.010), (I-130)+(17.011), (I-130)+(17.012) and (I-130)+(18.001).

Also preferred compound combinations are selected from group (G3-1) consisting of the following mixtures:

(I-300)+(1.001), (I-300)+(1.002), (I-300)+(1.003), (I-300)+(1.004), (I-300)+(1.005), (I-300)+(1.006), (I-300)+(1.007), (I-300)+(1.008), (I-300)+(1.009), (I-300)+(1.010), (I-300)+(1.011), (I-300)+(1.012), (I-300)+(1.013), (I-300)+(1.014), (I-300)+(1.015), (I-300)+(1.016), (I-300)+(1.017), (I-300)+(1.018), (I-300)+(1.019), (I-300)+(1.020), (I-300)+(1.021), (I-300)+(1.022), (I-300)+(1.023), (I-300)+(1.024), (I-300)+(1.025), (I-300)+(1.026), (I-300)+(1.027), (I-300)+(1.028), (I-300)+(1.029), (I-300)+(1.030), (I-300)+(1.031), (I-300)+(1.032), (I-300)+(1.033), (I-300)+(1.034), (I-300)+(1.035), (I-300)+(1.036), (I-300)+(1.037), (I-300)+(1.038), (I-300)+(1.039), (I-300)+(1.040), (I-300)+(1.041), (I-300)+(1.042), (I-300)+(1.043), (I-300)+(1.044), (I-300)+(1.045), (I-300)+(1.046), (I-300)+(1.047), (I-300)+(1.048), (I-300)+(1.049), (I-300)+(1.050), (I-300)+(1.051), (I-300)+(1.052), (I-300)+(1.053), (I-300)+(1.054), (I-300)+(1.055), (I-300)+(1.056), (I-300)+(1.057), (I-300)+(1.058), (I-300)+(1.059), (I-300)+(1.060), (I-300)+(1.061), (I-300)+(1.062), (I-300)+(1.063), (I-300)+(1.064), (I-300)+(1.065), (I-300)+(1.066), (I-300)+(1.067), (I-300)+(1.068), (I-300)+(1.069), (I-300)+(1.070), (I-300)+(1.071), (I-300)+(1.072), (I-300)+(1.073), (I-300)+(1.074), (I-300)+(1.075), (I-300)+(1.076), (I-300)+(1.077), (I-300)+(1.078), (I-300)+(1.079), (I-300)+(1.080), (I-300)+(1.081), (I-300)+(1.082), (I-300)+(1.083), (I-300)+(1.084), (I-300)+(1.085), (I-300)+(1.086), (I-300)+(1.087), (I-300)+(1.088), (I-300)+(1.089), (I-300)+(1.090), (I-300)+(1.091), (I-300)+(1.092), (I-300)+(2.001), (I-300)+(2.002), (I-300)+(2.003), (I-300)+(2.004), (I-300)+(2.005), (I-300)+(2.006), (I-300)+(2.007), (I-300)+(2.008), (I-300)+(2.009), (I-300)+(2.010), (I-300)+(2.011), (I-300)+(2.012), (I-300)+(2.013), (I-300)+(2.014), (I-300)+(2.015), (I-300)+(2.016), (I-300)+(2.017), (I-300)+(2.018), (I-300)+(2.019), (I-300)+(2.020), (I-300)+(2.021), (I-300)+(2.022), (I-300)+(2.023), (I-300)+(2.024), (I-300)+(2.025), (I-300)+(2.026), (I-300)+(2.027), (I-300)+(2.028), (I-300)+(2.029), (I-300)+(2.030), (I-300)+(2.031), (I-300)+(2.032), (I-300)+(2.033), (I-300)+(2.034), (I-300)+(2.035), (I-300)+(2.036), (I-300)+(2.037), (I-300)+(2.038), (I-300)+(2.039), (I-300)+(2.040), (I-300)+(2.041), (I-300)+(2.042), (I-300)+(2.043), (I-300)+(2.044), (I-300)+(2.045), (I-300)+(2.046), (I-300)+(2.047), (I-300)+(2.048), (I-300)+(2.049), (I-300)+(2.050), (I-300)+(2.051), (I-300)+(2.052), (I-300)+(2.053), (I-300)+(2.054), (I-300)+(2.055), (I-300)+(2.056), (I-300)+(2.057), (I-300)+(2.058), (I-300)+(2.059), (I-300)+(2.060), (I-300)+(3.001), (I-300)+(3.002), (I-300)+(3.003), (I-300)+(3.004), (I-300)+(3.005), (I-300)+(3.006), (I-300)+(3.007), (I-300)+(3.008), (I-300)+(3.009), (I-300)+(3.010), (I-300)+(3.011), (I-300)+(3.012), (I-300)+(3.013), (I-300)+(3.014), (I-300)+(3.015), (I-300)+(3.016), (I-300)+(3.017), (I-300)+(3.018), (I-300)+(3.019), (I-300)+(3.020), (I-300)+(3.021), (I-300)+(3.022), (I-300)+(3.023), (I-300)+(3.024), (I-300)+(3.025), (I-300)+(3.026), (I-300)+(3.027), (I-300)+(3.028), (I-300)+(3.029), (I-300)+(3.030), (I-300)+(3.031), (I-300)+(3.032), (I-300)+(4.001), (I-300)+(4.002), (I-300)+(4.003), (I-300)+(4.004), (I-300)+(4.005), (I-300)+(4.006), (I-300)+(4.007), (I-300)+(4.008), (I-300)+(4.009), (I-300)+(4.010), (I-300)+(4.011), (I-300)+(4.012), (I-300)+(4.013), (I-300)+(4.014), (I-300)+(4.015), (I-300)+(4.016), (I-300)+(4.017), (I-300)+(4.018), (I-300)+(4.019), (I-300)+(4.020), (I-300)+(4.021), (I-300)+(4.022), (I-300)+(4.023), (I-300)+(4.024), (I-300)+(4.025), (I-300)+(4.026), (I-300)+(5.001), (I-300)+(5.002), (I-300)+(5.003), (I-300)+(5.004), (I-300)+(5.005), (I-300)+(5.006), (I-300)+(5.007), (I-300)+(5.008), (I-300)+(5.009), (I-300)+(5.010), (I-300)+(5.011), (I-300)+(5.012), (I-300)+(5.013), (I-300)+(5.014), (I-300)+(5.015), (I-300)+(5.016), (I-300)+(5.017), (I-300)+(5.018), (I-300)+(5.019), (I-300)+(5.020), (I-300)+(5.021), (I-300)+(5.022), (I-300)+(5.023), (I-300)+(6.001), (I-300)+(6.002), (I-300)+(6.003), (I-300)+(6.004), (I-300)+(7.001), (I-300)+(7.002), (I-300)+(7.003), (I-300)+(7.004), (I-300)+(7.005), (I-300)+(7.006), (I-300)+(8.001), (I-300)+(9.001), (I-300)+(9.002), (I-300)+(9.003), (I-300)+(9.004), (I-300)+(9.005), (I-300)+(9.006), (I-300)+(9.007), (I-300)+(9.008), (I-300)+(9.009), (I-300)+(10.001), (I-300)+(10.002), (I-300)+(10.003), (I-300)+(11.001), (I-300)+(11.002), (I-300)+(12.001), (I-300)+(12.002), (I-300)+(12.003), (I-300)+(12.004), (I-300)+(13.001), (I-300)+(13.002), (I-300)+(13.003), (I-300)+(13.004), (I-300)+(13.005), (I-300)+(13.006), (I-300)+(14.001), (I-300)+(14.002), (I-300)+(15.001), (I-300)+(15.002), (I-300)+(15.003), (I-300)+(15.004), (I-300)+(15.005), (I-300)+(15.006), (I-300)+(15.007), (I-300)+(15.008), (I-300)+(15.009), (I-300)+(15.010), (I-300)+(15.011), (I-300)+(15.012), (I-300)+(15.013), (I-300)+(15.014), (I-300)+(15.015), (I-300)+(15.016), (I-300)+(15.017), (I-300)+(15.018), (I-300)+(15.019), (I-300)+(15.020), (I-300)+(15.021), (I-300)+(15.022), (I-300)+(15.023), (I-300)+(15.024), (I-300)+(15.025), (I-300)+(15.026), (I-300)+(15.027), (I-300)+(15.028), (I-300)+(15.029), (I-300)+(15.030), (I-300)+(15.031), (I-300)+(15.032), (I-300)+(15.033), (I-300)+(15.034), (I-300)+(15.035), (I-300)+(15.036), (I-300)+(15.037), (I-300)+(15.038), (I-300)+(15.039), (I-300)+(15.040), (I-300)+(15.041), (I-300)+(15.042), (I-300)+(15.043), (I-300)+(15.044), (I-300)+(15.045), (I-300)+(15.046), (I-300)+(15.047), (I-300)+(15.048), (I-300)+(15.049), (I-300)+(15.050), (I-300)+(15.051), (I-300)+(15.052), (I-300)+(15.053), (I-300)+(15.054), (I-300)+(15.055), (I-300)+(15.056), (I-300)+(15.057), (I-300)+(15.058), (I-300)+(15.059), (I-300)+(15.060), (I-300)+(15.061), (I-300)+(15.062), (I-300)+(15.063), (I-300)+(15.064), (I-300)+(15.065), (I-300)+(15.066), (I-300)+(15.067), (I-300)+(15.068), (I-300)+(15.069), (I-300)+(15.070), (I-300)+(15.071), (I-300)+(15.072), (I-300)+(15.073), (I-300)+(15.074), (I-300)+(15.075), (I-300)+(15.076), (I-300)+(15.077), (I-300)+(15.078), (I-300)+(15.079), (I-300)+(15.080), (I-300)+(15.081), (I-300)+(15.082), (I-300)+(15.083), (I-300)+(15.084), (I-300)+(15.085), (I-300)+(15.086), (I-300)+(15.087), (I-300)+(15.088), (I-300)+(15.089), (I-300)+(15.090), (I-300)+(15.091), (I-300)+(15.092), (I-300)+(15.093), (I-300)+(15.094), (I-300)+(15.095), (I-300)+(15.096), (I-300)+(15.097), (I-300)+(15.098), (I-300)+(15.099), (I-300)+(15.100), (I-300)+(15.101), (I-300)+(15.102), (I-300)+(15.103), (I-300)+(15.104), (I-300)+(15.105), (I-300)+(15.106), (I-300)+(15.107), (I-300)+(15.108), (I-300)+(15.109), (I-300)+(15.110), (I-300)+(15.111), (I-300)+(15.112), (I-300)+(15.113), (I-300)+(15.114), (I-300)+(15.115), (I-300)+(15.116), (I-300)+(15.117), (I-300)+(15.118), (I-300)+(15.119), (I-300)+(15.120), (I-300)+(15.121), (I-300)+(15.122), (I-300)+(15.123), (I-300)+(15.124), (I-300)+(15.125), (I-300)+(15.126), (I-300)+(15.127), (I-300)+(15.128), (I-300)+(16.001), (I-300)+(16.002), (I-300)+(16.003), (I-300)+(16.004), (I-300)+(16.005), (I-300)+(16.006), (I-300)+(16.007), (I-300)+(16.008), (I-300)+(17.001), (I-300)+(17.002), (I-300)+(17.003), (I-300)+(17.004), (I-300)+(17.005), (I-300)+(17.006), (I-300)+(17.007), (I-300)+(17.008), (I-300)+(17.009), (I-300)+(17.010), (I-300)+(17.011), (I-300)+(17.012) and (I-300)+(18.001).

Also preferred compound combinations are selected from group (G3) consisting of the following mixtures:

(I-300)+(1.001), (I-300)+(1.002), (I-300)+(1.003), (I-300)+(1.004), (I-300)+(1.005), (I-300)+(1.006), (I-300)+(1.007), (I-300)+(1.008), (I-300)+(1.009), (I-300)+(1.010), (I-300)+(1.011), (I-300)+(1.012), (I-300)+(1.013), (I-300)+(1.014), (I-300)+(1.015), (I-300)+(1.016), (I-300)+(1.017), (I-300)+(1.018), (I-300)+(1.019), (I-300)+(1.020), (I-300)+(1.021), (I-300)+(1.022), (I-300)+(1.023), (I-300)+(1.024), (I-300)+(1.025), (I-300)+(1.026), (I-300)+(1.027), (I-300)+(1.028), (I-300)+(1.029), (I-300)+(1.030), (I-300)+(1.031), (I-300)+(1.032), (I-300)+(1.033), (I-300)+(1.034), (I-300)+(1.035), (I-300)+(1.036), (I-300)+(1.037), (I-300)+(1.038), (I-300)+(1.039), (I-300)+(1.040), (I-300)+(1.041), (I-300)+(1.042), (I-300)+(1.043), (I-300)+(1.044), (I-300)+(1.045), (I-300)+(1.046), (I-300)+(1.047), (I-300)+(1.048), (I-300)+(1.049), (I-300)+(1.050), (I-300)+(1.051), (I-300)+(1.052), (I-300)+(1.053), (I-300)+(1.054), (I-300)+(1.055), (I-300)+(1.056), (I-300)+(1.057), (I-300)+(1.058), (I-300)+(1.059), (I-300)+(1.060), (I-300)+(1.061), (I-300)+(1.062), (I-300)+(1.063), (I-300)+(1.064), (I-300)+(1.065), (I-300)+(1.066), (I-300)+(1.067), (I-300)+(1.068), (I-300)+(1.069), (I-300)+(1.070), (I-300)+(1.071), (I-300)+(1.072), (I-300)+(1.073), (I-300)+(1.074), (I-300)+(1.075), (I-300)+(1.076), (I-300)+(1.077), (I-300)+(1.078), (I-300)+(1.079), (I-300)+(1.080), (I-300)+(1.081), (I-300)+(1.082), (I-300)+(1.083), (I-300)+(1.084), (I-300)+(1.085), (I-300)+(1.086), (I-300)+(1.087), (I-300)+(1.088), (I-300)+(1.089), (I-300)+(1.090), (I-300)+(1.091), (I-300)+(1.092), (I-300)+(2.001), (I-300)+(2.002), (I-300)+(2.003), (I-300)+(2.004), (I-300)+(2.005), (I-300)+(2.006), (I-300)+(2.007), (I-300)+(2.008), (I-300)+(2.009), (I-300)+(2.010), (I-300)+(2.011), (I-300)+(2.012), (I-300)+(2.013), (I-300)+(2.014), (I-300)+(2.015), (I-300)+(2.016), (I-300)+(2.017), (I-300)+(2.018), (I-300)+(2.019), (I-300)+(2.020), (I-300)+(2.021), (I-300)+(2.022), (I-300)+(2.023), (I-300)+(2.024), (I-300)+(2.025), (I-300)+(2.026), (I-300)+(2.027), (I-300)+(2.028), (I-300)+(2.029), (I-300)+(2.030), (I-300)+(2.031), (I-300)+(2.032), (I-300)+(2.033), (I-300)+(2.034), (I-300)+(2.035), (I-300)+(2.036), (I-300)+(2.037), (I-300)+(2.038), (I-300)+(2.039), (I-300)+(2.040), (I-300)+(2.041), (I-300)+(2.042), (I-300)+(2.043), (I-300)+(2.044), (I-300)+(2.045), (I-300)+(2.046), (I-300)+(2.047), (I-300)+(2.048), (I-300)+(2.049), (I-300)+(2.050), (I-300)+(2.051), (I-300)+(2.052), (I-300)+(2.053), (I-300)+(2.054), (I-300)+(2.055), (I-300)+(2.056), (I-300)+(2.057), (I-300)+(2.058), (I-300)+(2.059), (I-300)+(3.001), (I-300)+(3.002), (I-300)+(3.003), (I-300)+(3.004), (I-300)+(3.005), (I-300)+(3.006), (I-300)+(3.007), (I-300)+(3.008), (I-300)+(3.009), (I-300)+(3.010), (I-300)+(3.011), (I-300)+(3.012), (I-300)+(3.013), (I-300)+(3.014), (I-300)+(3.015), (I-300)+(3.016), (I-300)+(3.017), (I-300)+(3.018), (I-300)+(3.019), (I-300)+(3.020), (I-300)+(3.021), (I-300)+(3.022), (I-300)+(3.023), (I-300)+(3.024), (I-300)+(3.025), (I-300)+(3.026), (I-300)+(3.027), (I-300)+(3.028), (I-300)+(3.029), (I-300)+(3.030), (I-300)+(3.031), (I-300)+(4.001), (I-300)+(4.002), (I-300)+(4.003), (I-300)+(4.004), (I-300)+(4.005), (I-300)+(4.006), (I-300)+(4.007), (I-300)+(4.008), (I-300)+(4.009), (I-300)+(4.010), (I-300)+(4.011), (I-300)+(4.012), (I-300)+(4.013), (I-300)+(4.014), (I-300)+(4.015), (I-300)+(4.016), (I-300)+(4.017), (I-300)+(4.018), (I-300)+(4.019), (I-300)+(4.020), (I-300)+(4.021), (I-300)+(4.022), (I-300)+(4.023), (I-300)+(4.024), (I-300)+(4.025), (I-300)+(4.026), (I-300)+(5.001), (I-300)+(5.002), (I-300)+(5.003), (I-300)+(5.004), (I-300)+(5.005), (I-300)+(5.006), (I-300)+(5.007), (I-300)+(5.008), (I-300)+(5.009), (I-300)+(5.010), (I-300)+(5.011), (I-300)+(5.012), (I-300)+(5.013), (I-300)+(5.014), (I-300)+(5.015), (I-300)+(5.016), (I-300)+(5.017), (I-300)+(5.018), (I-300)+(5.019), (I-300)+(5.020), (I-300)+(5.021), (I-300)+(5.022), (I-300)+(5.023), (I-300)+(6.001), (I-300)+(6.002), (I-300)+(6.003), (I-300)+(6.004), (I-300)+(7.001), (I-300)+(7.002), (I-300)+(7.003), (I-300)+(7.004), (I-300)+(7.005), (I-300)+(7.006), (I-300)+(8.001), (I-300)+(9.001), (I-300)+(9.002), (I-300)+(9.003), (I-300)+(9.004), (I-300)+(9.005), (I-300)+(9.006), (I-300)+(9.007), (I-300)+(9.008), (I-300)+(9.009), (I-300)+(10.001), (I-300)+(10.002), (I-300)+(10.003), (I-300)+(11.001), (I-300)+(11.002), (I-300)+(12.001), (I-300)+(12.002), (I-300)+(12.003), (I-300)+(12.004), (I-300)+(13.001), (I-300)+(13.002), (I-300)+(13.003), (I-300)+(13.004), (I-300)+(13.005), (I-300)+(13.006), (I-300)+(14.001), (I-300)+(14.002), (I-300)+(15.001), (I-300)+(15.002), (I-300)+(15.003), (I-300)+(15.004), (I-300)+(15.005), (I-300)+(15.006), (I-300)+(15.007), (I-300)+(15.008), (I-300)+(15.009), (I-300)+(15.010), (I-300)+(15.011), (I-300)+(15.012), (I-300)+(15.013), (I-300)+(15.014), (I-300)+(15.015), (I-300)+(15.016), (I-300)+(15.017), (I-300)+(15.018), (I-300)+(15.019), (I-300)+(15.020), (I-300)+(15.021), (I-300)+(15.022), (I-300)+(15.023), (I-300)+(15.024), (I-300)+(15.025), (I-300)+(15.026), (I-300)+(15.027), (I-300)+(15.028), (I-300)+(15.029), (I-300)+(15.030), (I-300)+(15.031), (I-300)+(15.032), (I-300)+(15.033), (I-300)+(15.034), (I-300)+(15.035), (I-300)+(15.036), (I-300)+(15.037), (I-300)+(15.038), (I-300)+(15.039), (I-300)+(15.040), (I-300)+(15.041), (I-300)+(15.042), (I-300)+(15.043), (I-300)+(15.044), (I-300)+(15.045), (I-300)+(15.046), (I-300)+(15.047), (I-300)+(15.048), (I-300)+(15.049), (I-300)+(15.050), (I-300)+(15.051), (I-300)+(15.052), (I-300)+(15.053), (I-300)+(15.054), (I-300)+(15.055), (I-300)+(15.056), (I-300)+(15.057), (I-300)+(15.058), (I-300)+(15.059), (I-300)+(15.060), (I-300)+(15.061), (I-300)+(15.062), (I-300)+(15.063), (I-300)+(15.064), (I-300)+(15.065), (I-300)+(15.066), (I-300)+(15.067), (I-300)+(15.068), (I-300)+(15.069), (I-300)+(15.070), (I-300)+(15.071), (I-300)+(15.072), (I-300)+(15.073), (I-300)+(15.074), (I-300)+(15.075), (I-300)+(15.076), (I-300)+(15.077), (I-300)+(15.078), (I-300)+(15.079), (I-300)+(15.080), (I-300)+(15.081), (I-300)+(15.082), (I-300)+(15.083), (I-300)+(15.084), (I-300)+(15.085), (I-300)+(15.086), (I-300)+(15.087), (I-300)+(15.088), (I-300)+(15.089), (I-300)+(15.090), (I-300)+(15.091), (I-300)+(15.092), (I-300)+(15.093), (I-300)+(15.094), (I-300)+(15.095), (I-300)+(15.096), (I-300)+(15.097), (I-300)+(15.098), (I-300)+(15.099), (I-300)+(15.100), (I-300)+(15.101), (I-300)+(15.102), (I-300)+(15.103), (I-300)+(15.104), (I-300)+(15.105), (I-300)+(15.106), (I-300)+(15.107), (I-300)+(15.108), (I-300)+(15.109), (I-300)+(15.110), (I-300)+(15.111), (I-300)+(15.112), (I-300)+(15.113), (I-300)+(15.114), (I-300)+(15.115), (I-300)+(15.116), (I-300)+(15.117), (I-300)+(15.118), (I-300)+(15.119), (I-300)+(15.120), (I-300)+(15.121), (I-300)+(15.122), (I-300)+(15.123), (I-300)+(15.124), (I-300)+(15.125), (I-300)+(15.126), (I-300)+(15.127), (I-300)+(16.001), (I-300)+(16.002), (I-300)+(16.003), (I-300)+(16.004), (I-300)+(16.005), (I-300)+(16.006), (I-300)+(16.007), (I-300)+(16.008), (I-300)+(17.001), (I-300)+(17.002), (I-300)+(17.003), (I-300)+(17.004), (I-300)+(17.005), (I-300)+(17.006), (I-300)+(17.007), (I-300)+(17.008), (I-300)+(17.009), (I-300)+(17.010), (I-300)+(17.011), (I-300)+(17.012) and (I-300)+(18.001).

Also preferred compound combinations are selected from group (G4-1) consisting of the following mixtures:

(I-302)+(1.001), (I-302)+(1.002), (I-302)+(1.003), (I-302)+(1.004), (I-302)+(1.005), (I-302)+(1.006), (I-302)+(1.007), (I-302)+(1.008), (I-302)+(1.009), (I-302)+(1.010), (I-302)+(1.011), (I-302)+(1.012), (I-302)+(1.013), (I-302)+(1.014), (I-302)+(1.015), (I-302)+(1.016), (I-302)+(1.017), (I-302)+(1.018), (I-302)+(1.019), (I-302)+(1.020), (I-302)+(1.021), (I-302)+(1.022), (I-302)+(1.023), (I-302)+(1.024), (I-302)+(1.025), (I-302)+(1.026), (I-302)+(1.027), (I-302)+(1.028), (I-302)+(1.029), (I-302)+(1.030), (I-302)+(1.031), (I-302)+(1.032), (I-302)+(1.033), (I-302)+(1.034), (I-302)+(1.035), (I-302)+(1.036), (I-302)+(1.037), (I-302)+(1.038), (I-302)+(1.039), (I-302)+(1.040), (I-302)+(1.041), (I-302)+(1.042), (I-302)+(1.043), (I-302)+(1.044), (I-302)+(1.045), (I-302)+(1.046), (I-302)+(1.047), (I-302)+(1.048), (I-302)+(1.049), (I-302)+(1.050), (I-302)+(1.051), (I-302)+(1.052), (I-302)+(1.053), (I-302)+(1.054), (I-302)+(1.055), (I-302)+(1.056), (I-302)+(1.057), (I-302)+(1.058), (I-302)+(1.059), (I-302)+(1.060), (I-302)+(1.061), (I-302)+(1.062), (I-302)+(1.063), (I-302)+(1.064), (I-302)+(1.065), (I-302)+(1.066), (I-302)+(1.067), (I-302)+(1.068), (I-302)+(1.069), (I-302)+(1.070), (I-302)+(1.071), (I-302)+(1.072), (I-302)+(1.073), (I-302)+(1.074), (I-302)+(1.075), (I-302)+(1.076), (I-302)+(1.077), (I-302)+(1.078), (I-302)+(1.079), (I-302)+(1.080), (I-302)+(1.081), (I-302)+(1.082), (I-302)+(1.083), (I-302)+(1.084), (I-302)+(1.085), (I-302)+(1.086), (I-302)+(1.087), (I-302)+(1.088), (I-302)+(1.089), (I-302)+(1.090), (I-302)+(1.091), (I-302)+(1.092), (I-302)+(2.001), (I-302)+(2.002), (I-302)+(2.003), (I-302)+(2.004), (I-302)+(2.005), (I-302)+(2.006), (I-302)+(2.007), (I-302)+(2.008), (I-302)+(2.009), (I-302)+(2.010), (I-302)+(2.011), (I-302)+(2.012), (I-302)+(2.013), (I-302)+(2.014), (I-302)+(2.015), (I-302)+(2.016), (I-302)+(2.017), (I-302)+(2.018), (I-302)+(2.019), (I-302)+(2.020), (I-302)+(2.021), (I-302)+(2.022), (I-302)+(2.023), (I-302)+(2.024), (I-302)+(2.025), (I-302)+(2.026), (I-302)+(2.027), (I-302)+(2.028), (I-302)+(2.029), (I-302)+(2.030), (I-302)+(2.031), (I-302)+(2.032), (I-302)+(2.033), (I-302)+(2.034), (I-302)+(2.035), (I-302)+(2.036), (I-302)+(2.037), (I-302)+(2.038), (I-302)+(2.039), (I-302)+(2.040), (I-302)+(2.041), (I-302)+(2.042), (I-302)+(2.043), (I-302)+(2.044), (I-302)+(2.045), (I-302)+(2.046), (I-302)+(2.047), (I-302)+(2.048), (I-302)+(2.049), (I-302)+(2.050), (I-302)+(2.051), (I-302)+(2.052), (I-302)+(2.053), (I-302)+(2.054), (I-302)+(2.055), (I-302)+(2.056), (I-302)+(2.057), (I-302)+(2.058), (I-302)+(2.059), (I-302)+(2.060), (I-302)+(3.001), (I-302)+(3.002), (I-302)+(3.003), (I-302)+(3.004), (I-302)+(3.005), (I-302)+(3.006), (I-302)+(3.007), (I-302)+(3.008), (I-302)+(3.009), (I-302)+(3.010), (I-302)+(3.011), (I-302)+(3.012), (I-302)+(3.013), (I-302)+(3.014), (I-302)+(3.015), (I-302)+(3.016), (I-302)+(3.017), (I-302)+(3.018), (I-302)+(3.019), (I-302)+(3.020), (I-302)+(3.021), (I-302)+(3.022), (I-302)+(3.023), (I-302)+(3.024), (I-302)+(3.025), (I-302)+(3.026), (I-302)+(3.027), (I-302)+(3.028), (I-302)+(3.029), (I-302)+(3.030), (I-302)+(3.031), (I-302)+(3.032), (I-302)+(4.001), (I-302)+(4.002), (I-302)+(4.003), (I-302)+(4.004), (I-302)+(4.005), (I-302)+(4.006), (I-302)+(4.007), (I-302)+(4.008), (I-302)+(4.009), (I-302)+(4.010), (I-302)+(4.011), (I-302)+(4.012), (I-302)+(4.013), (I-302)+(4.014), (I-302)+(4.015), (I-302)+(4.016), (I-302)+(4.017), (I-302)+(4.018), (I-302)+(4.019), (I-302)+(4.020), (I-302)+(4.021), (I-302)+(4.022), (I-302)+(4.023), (I-302)+(4.024), (I-302)+(4.025), (I-302)+(4.026), (I-302)+(5.001), (I-302)+(5.002), (I-302)+(5.003), (I-302)+(5.004), (I-302)+(5.005), (I-302)+(5.006), (I-302)+(5.007), (I-302)+(5.008), (I-302)+(5.009), (I-302)+(5.010), (I-302)+(5.011), (I-302)+(5.012), (I-302)+(5.013), (I-302)+(5.014), (I-302)+(5.015), (I-302)+(5.016), (I-302)+(5.017), (I-302)+(5.018), (I-302)+(5.019), (I-302)+(5.020), (I-302)+(5.021), (I-302)+(5.022), (I-302)+(5.023), (I-302)+(6.001), (I-302)+(6.002), (I-302)+(6.003), (I-302)+(6.004), (I-302)+(7.001), (I-302)+(7.002), (I-302)+(7.003), (I-302)+(7.004), (I-302)+(7.005), (I-302)+(7.006), (I-302)+(8.001), (I-302)+(9.001), (I-302)+(9.002), (I-302)+(9.003), (I-302)+(9.004), (I-302)+(9.005), (I-302)+(9.006), (I-302)+(9.007), (I-302)+(9.008), (I-302)+(9.009), (I-302)+(10.001), (I-302)+(10.002), (I-302)+(10.003), (I-302)+(11.001), (I-302)+(11.002), (I-302)+(12.001), (I-302)+(12.002), (I-302)+(12.003), (I-302)+(12.004), (I-302)+(13.001), (I-302)+(13.002), (I-302)+(13.003), (I-302)+(13.004), (I-302)+(13.005), (I-302)+(13.006), (I-302)+(14.001), (I-302)+(14.002), (I-302)+(15.001), (I-302)+(15.002), (I-302)+(15.003), (I-302)+(15.004), (I-302)+(15.005), (I-302)+(15.006), (I-302)+(15.007), (I-302)+(15.008), (I-302)+(15.009), (I-302)+(15.010), (I-302)+(15.011), (I-302)+(15.012), (I-302)+(15.013), (I-302)+(15.014), (I-302)+(15.015), (I-302)+(15.016), (I-302)+(15.017), (I-302)+(15.018), (I-302)+(15.019), (I-302)+(15.020), (I-302)+(15.021), (I-302)+(15.022), (I-302)+(15.023), (I-302)+(15.024), (I-302)+(15.025), (I-302)+(15.026), (I-302)+(15.027), (I-302)+(15.028), (I-302)+(15.029), (I-302)+(15.030), (I-302)+(15.031), (I-302)+(15.032), (I-302)+(15.033), (I-302)+(15.034), (I-302)+(15.035), (I-302)+(15.036), (I-302)+(15.037), (I-302)+(15.038), (I-302)+(15.039), (I-302)+(15.040), (I-302)+(15.041), (I-302)+(15.042), (I-302)+(15.043), (I-302)+(15.044), (I-302)+(15.045), (I-302)+(15.046), (I-302)+(15.047), (I-302)+(15.048), (I-302)+(15.049), (I-302)+(15.050), (I-302)+(15.051), (I-302)+(15.052), (I-302)+(15.053), (I-302)+(15.054), (I-302)+(15.055), (I-302)+(15.056), (I-302)+(15.057), (I-302)+(15.058), (I-302)+(15.059), (I-302)+(15.060), (I-302)+(15.061), (I-302)+(15.062), (I-302)+(15.063), (I-302)+(15.064), (I-302)+(15.065), (I-302)+(15.066), (I-302)+(15.067), (I-302)+(15.068), (I-302)+(15.069), (I-302)+(15.070), (I-302)+(15.071), (I-302)+(15.072), (I-302)+(15.073), (I-302)+(15.074), (I-302)+(15.075), (I-302)+(15.076), (I-302)+(15.077), (I-302)+(15.078), (I-302)+(15.079), (I-302)+(15.080), (I-302)+(15.081), (I-302)+(15.082), (I-302)+(15.083), (I-302)+(15.084), (I-302)+(15.085), (I-302)+(15.086), (I-302)+(15.087), (I-302)+(15.088), (I-302)+(15.089), (I-302)+(15.090), (I-302)+(15.091), (I-302)+(15.092), (I-302)+(15.093), (I-302)+(15.094), (I-302)+(15.095), (I-302)+(15.096), (I-302)+(15.097), (I-302)+(15.098), (I-302)+(15.099), (I-302)+(15.100), (I-302)+(15.101), (I-302)+(15.102), (I-302)+(15.103), (I-302)+(15.104), (I-302)+(15.105), (I-302)+(15.106), (I-302)+(15.107), (I-302)+(15.108), (I-302)+(15.109), (I-302)+(15.110), (I-302)+(15.111), (I-302)+(15.112), (I-302)+(15.113), (I-302)+(15.114), (I-302)+(15.115), (I-302)+(15.116), (I-302)+(15.117), (I-302)+(15.118), (I-302)+(15.119), (I-302)+(15.120), (I-302)+(15.121), (I-302)+(15.122), (I-302)+(15.123), (I-302)+(15.124), (I-302)+(15.125), (I-302)+(15.126), (I-302)+(15.127), (I-302)+(15.128), (I-302)+(16.001), (I-302)+(16.002), (I-302)+(16.003), (I-302)+(16.004), (I-302)+(16.005), (I-302)+(16.006), (I-302)+(16.007), (I-302)+(16.008), (I-302)+(17.001), (I-302)+(17.002), (I-302)+(17.003), (I-302)+(17.004), (I-302)+(17.005), (I-302)+(17.006), (I-302)+(17.007), (I-302)+(17.008), (I-302)+(17.009), (I-302)+(17.010), (I-302)+(17.011), (I-302)+(17.012) and (I-302)+(18.001).

Also preferred compound combinations are selected from group (G4) consisting of the following mixtures:

(I-302)+(1.001), (I-302)+(1.002), (I-302)+(1.003), (I-302)+(1.004), (I-302)+(1.005), (I-302)+(1.006), (I-302)+(1.007), (I-302)+(1.008), (I-302)+(1.009), (I-302)+(1.010), (I-302)+(1.011), (I-302)+(1.012), (I-302)+(1.013), (I-302)+(1.014), (I-302)+(1.015), (I-302)+(1.016), (I-302)+(1.017), (I-302)+(1.018), (I-302)+(1.019), (I-302)+(1.020), (I-302)+(1.021), (I-302)+(1.022), (I-302)+(1.023), (I-302)+(1.024), (I-302)+(1.025), (I-302)+(1.026), (I-302)+(1.027), (I-302)+(1.028), (I-302)+(1.029), (I-302)+(1.030), (I-302)+(1.031), (I-302)+(1.032), (I-302)+(1.033), (I-302)+(1.034), (I-302)+(1.035), (I-302)+(1.036), (I-302)+(1.037), (I-302)+(1.038), (I-302)+(1.039), (I-302)+(1.040), (I-302)+(1.041), (I-302)+(1.042), (I-302)+(1.043), (I-302)+(1.044), (I-302)+(1.045), (I-302)+(1.046), (I-302)+(1.047), (I-302)+(1.048), (I-302)+(1.049), (I-302)+(1.050), (I-302)+(1.051), (I-302)+(1.052), (I-302)+(1.053), (I-302)+(1.054), (I-302)+(1.055), (I-302)+(1.056), (I-302)+(1.057), (I-302)+(1.058), (I-302)+(1.059), (I-302)+(1.060), (I-302)+(1.061), (I-302)+(1.062), (I-302)+(1.063), (I-302)+(1.064), (I-302)+(1.065), (I-302)+(1.066), (I-302)+(1.067), (I-302)+(1.068), (I-302)+(1.069), (I-302)+(1.070), (I-302)+(1.071), (I-302)+(1.072), (I-302)+(1.073), (I-302)+(1.074), (I-302)+(1.075), (I-302)+(1.076), (I-302)+(1.077), (I-302)+(1.078), (I-302)+(1.079), (I-302)+(1.080), (I-302)+(1.081), (I-302)+(1.082), (I-302)+(1.083), (I-302)+(1.084), (I-302)+(1.085), (I-302)+(1.086), (I-302)+(1.087), (I-302)+(1.088), (I-302)+(1.089), (I-302)+(1.090), (I-302)+(1.091), (I-302)+(1.092), (I-302)+(2.001), (I-302)+(2.002), (I-302)+(2.003), (I-302)+(2.004), (I-302)+(2.005), (I-302)+(2.006), (I-302)+(2.007), (I-302)+(2.008), (I-302)+(2.009), (I-302)+(2.010), (I-302)+(2.011), (I-302)+(2.012), (I-302)+(2.013), (I-302)+(2.014), (I-302)+(2.015), (I-302)+(2.016), (I-302)+(2.017), (I-302)+(2.018), (I-302)+(2.019), (I-302)+(2.020), (I-302)+(2.021), (I-302)+(2.022), (I-302)+(2.023), (I-302)+(2.024), (I-302)+(2.025), (I-302)+(2.026), (I-302)+(2.027), (I-302)+(2.028), (I-302)+(2.029), (I-302)+(2.030), (I-302)+(2.031), (I-302)+(2.032), (I-302)+(2.033), (I-302)+(2.034), (I-302)+(2.035), (I-302)+(2.036), (I-302)+(2.037), (I-302)+(2.038), (I-302)+(2.039), (I-302)+(2.040), (I-302)+(2.041), (I-302)+(2.042), (I-302)+(2.043), (I-302)+(2.044), (I-302)+(2.045), (I-302)+(2.046), (I-302)+(2.047), (I-302)+(2.048), (I-302)+(2.049), (I-302)+(2.050), (I-302)+(2.051), (I-302)+(2.052), (I-302)+(2.053), (I-302)+(2.054), (I-302)+(2.055), (I-302)+(2.056), (I-302)+(2.057), (I-302)+(2.058), (I-302)+(2.059), (I-302)+(3.001), (I-302)+(3.002), (I-302)+(3.003), (I-302)+(3.004), (I-302)+(3.005), (I-302)+(3.006), (I-302)+(3.007), (I-302)+(3.008), (I-302)+(3.009), (I-302)+(3.010), (I-302)+(3.011), (I-302)+(3.012), (I-302)+(3.013), (I-302)+(3.014), (I-302)+(3.015), (I-302)+(3.016), (I-302)+(3.017), (I-302)+(3.018), (I-302)+(3.019), (I-302)+(3.020), (I-302)+(3.021), (I-302)+(3.022), (I-302)+(3.023), (I-302)+(3.024), (I-302)+(3.025), (I-302)+(3.026), (I-302)+(3.027), (I-302)+(3.028), (I-302)+(3.029), (I-302)+(3.030), (I-302)+(3.031), (I-302)+(4.001), (I-302)+(4.002), (I-302)+(4.003), (I-302)+(4.004), (I-302)+(4.005), (I-302)+(4.006), (I-302)+(4.007), (I-302)+(4.008), (I-302)+(4.009), (I-302)+(4.010), (I-302)+(4.011), (I-302)+(4.012), (I-302)+(4.013), (I-302)+(4.014), (I-302)+(4.015), (I-302)+(4.016), (I-302)+(4.017), (I-302)+(4.018), (I-302)+(4.019), (I-302)+(4.020), (I-302)+(4.021), (I-302)+(4.022), (I-302)+(4.023), (I-302)+(4.024), (I-302)+(4.025), (I-302)+(4.026), (I-302)+(5.001), (I-302)+(5.002), (I-302)+(5.003), (I-302)+(5.004), (I-302)+(5.005), (I-302)+(5.006), (I-302)+(5.007), (I-302)+(5.008), (I-302)+(5.009), (I-302)+(5.010), (I-302)+(5.011), (I-302)+(5.012), (I-302)+(5.013), (I-302)+(5.014), (I-302)+(5.015), (I-302)+(5.016), (I-302)+(5.017), (I-302)+(5.018), (I-302)+(5.019), (I-302)+(5.020), (I-302)+(5.021), (I-302)+(5.022), (I-302)+(5.023), (I-302)+(6.001), (I-302)+(6.002), (I-302)+(6.003), (I-302)+(6.004), (I-302)+(7.001), (I-302)+(7.002), (I-302)+(7.003), (I-302)+(7.004), (I-302)+(7.005), (I-302)+(7.006), (I-302)+(8.001), (I-302)+(9.001), (I-302)+(9.002), (I-302)+(9.003), (I-302)+(9.004), (I-302)+(9.005), (I-302)+(9.006), (I-302)+(9.007), (I-302)+(9.008), (I-302)+(9.009), (I-302)+(10.001), (I-302)+(10.002), (I-302)+(10.003), (I-302)+(11.001), (I-302)+(11.002), (I-302)+(12.001), (I-302)+(12.002), (I-302)+(12.003), (I-302)+(12.004), (I-302)+(13.001), (I-302)+(13.002), (I-302)+(13.003), (I-302)+(13.004), (I-302)+(13.005), (I-302)+(13.006), (I-302)+(14.001), (I-302)+(14.002), (I-302)+(15.001), (I-302)+(15.002), (I-302)+(15.003), (I-302)+(15.004), (I-302)+(15.005), (I-302)+(15.006), (I-302)+(15.007), (I-302)+(15.008), (I-302)+(15.009), (I-302)+(15.010), (I-302)+(15.011), (I-302)+(15.012), (I-302)+(15.013), (I-302)+(15.014), (I-302)+(15.015), (I-302)+(15.016), (I-302)+(15.017), (I-302)+(15.018), (I-302)+(15.019), (I-302)+(15.020), (I-302)+(15.021), (I-302)+(15.022), (I-302)+(15.023), (I-302)+(15.024), (I-302)+(15.025), (I-302)+(15.026), (I-302)+(15.027), (I-302)+(15.028), (I-302)+(15.029), (I-302)+(15.030), (I-302)+(15.031), (I-302)+(15.032), (I-302)+(15.033), (I-302)+(15.034), (I-302)+(15.035), (I-302)+(15.036), (I-302)+(15.037), (I-302)+(15.038), (I-302)+(15.039), (I-302)+(15.040), (I-302)+(15.041), (I-302)+(15.042), (I-302)+(15.043), (I-302)+(15.044), (I-302)+(15.045), (I-302)+(15.046), (I-302)+(15.047), (I-302)+(15.048), (I-302)+(15.049), (I-302)+(15.050), (I-302)+(15.051), (I-302)+(15.052), (I-302)+(15.053), (I-302)+(15.054), (I-302)+(15.055), (I-302)+(15.056), (I-302)+(15.057), (I-302)+(15.058), (I-302)+(15.059), (I-302)+(15.060), (I-302)+(15.061), (I-302)+(15.062), (I-302)+(15.063), (I-302)+(15.064), (I-302)+(15.065), (I-302)+(15.066), (I-302)+(15.067), (I-302)+(15.068), (I-302)+(15.069), (I-302)+(15.070), (I-302)+(15.071), (I-302)+(15.072), (I-302)+(15.073), (I-302)+(15.074), (I-302)+(15.075), (I-302)+(15.076), (I-302)+(15.077), (I-302)+(15.078), (I-302)+(15.079), (I-302)+(15.080), (I-302)+(15.081), (I-302)+(15.082), (I-302)+(15.083), (I-302)+(15.084), (I-302)+(15.085), (I-302)+(15.086), (I-302)+(15.087), (I-302)+(15.088), (I-302)+(15.089), (I-302)+(15.090), (I-302)+(15.091), (I-302)+(15.092), (I-302)+(15.093), (I-302)+(15.094), (I-302)+(15.095), (I-302)+(15.096), (I-302)+(15.097), (I-302)+(15.098), (I-302)+(15.099), (I-302)+(15.100), (I-302)+(15.101), (I-302)+(15.102), (I-302)+(15.103), (I-302)+(15.104), (I-302)+(15.105), (I-302)+(15.106), (I-302)+(15.107), (I-302)+(15.108), (I-302)+(15.109), (I-302)+(15.110), (I-302)+(15.111), (I-302)+(15.112), (I-302)+(15.113), (I-302)+(15.114), (I-302)+(15.115), (I-302)+(15.116), (I-302)+(15.117), (I-302)+(15.118), (I-302)+(15.119), (I-302)+(15.120), (I-302)+(15.121), (I-302)+(15.122), (I-302)+(15.123), (I-302)+(15.124), (I-302)+(15.125), (I-302)+(15.126), (I-302)+(15.127), (I-302)+(16.1001), (I-302)+(16.1002), (I-302)+(16.1003), (I-302)+(16.1004), (I-302)+(16.1005), (I-302)+(16.2001), (I-302)+(16.2002), (I-302)+(16.2003), (I-302)+(17.001), (I-302)+(17.002), (I-302)+(17.003), (I-302)+(17.004), (I-302)+(17.005), (I-302)+(17.006), (I-302)+(17.007), (I-302)+(17.008), (I-302)+(17.009), (I-302)+(17.010), (I-302)+(17.011), (I-302)+(17.012) and (I-302)+(18.001).

Also preferred compound combinations are selected from group (G5-1) consisting of the following mixtures:

(I-337)+(1.001), (I-337)+(1.002), (I-337)+(1.003), (I-337)+(1.004), (I-337)+(1.005), (I-337)+(1.006), (I-337)+(1.007), (I-337)+(1.008), (I-337)+(1.009), (I-337)+(1.010), (I-337)+(1.011), (I-337)+(1.012), (I-337)+(1.013), (I-337)+(1.014), (I-337)+(1.015), (I-337)+(1.016), (I-337)+(1.017), (I-337)+(1.018), (I-337)+(1.019), (I-337)+(1.020), (I-337)+(1.021), (I-337)+(1.022), (I-337)+(1.023), (I-337)+(1.024), (I-337)+(1.025), (I-337)+(1.026), (I-337)+(1.027), (I-337)+(1.028), (I-337)+(1.029), (I-337)+(1.030), (I-337)+(1.031), (I-337)+(1.032), (I-337)+(1.033), (I-337)+(1.034), (I-337)+(1.035), (I-337)+(1.036), (I-337)+(1.037), (I-337)+(1.038), (I-337)+(1.039), (I-337)+(1.040), (I-337)+(1.041), (I-337)+(1.042), (I-337)+(1.043), (I-337)+(1.044), (I-337)+(1.045), (I-337)+(1.046), (I-337)+(1.047), (I-337)+(1.048), (I-337)+(1.049), (I-337)+(1.050), (I-337)+(1.051), (I-337)+(1.052), (I-337)+(1.053), (I-337)+(1.054), (I-337)+(1.055), (I-337)+(1.056), (I-337)+(1.057), (I-337)+(1.058), (I-337)+(1.059), (I-337)+(1.060), (I-337)+(1.061), (I-337)+(1.062), (I-337)+(1.063), (I-337)+(1.064), (I-337)+(1.065), (I-337)+(1.066), (I-337)+(1.067), (I-337)+(1.068), (I-337)+(1.069), (I-337)+(1.070), (I-337)+(1.071), (I-337)+(1.072), (I-337)+(1.073), (I-337)+(1.074), (I-337)+(1.075), (I-337)+(1.076), (I-337)+(1.077), (I-337)+(1.078), (I-337)+(1.079), (I-337)+(1.080), (I-337)+(1.081), (I-337)+(1.082), (I-337)+(1.083), (I-337)+(1.084), (I-337)+(1.085), (I-337)+(1.086), (I-337)+(1.087), (I-337)+(1.088), (I-337)+(1.089), (I-337)+(1.090), (I-337)+(1.091), (I-337)+(1.092), (I-337)+(2.001), (I-337)+(2.002), (I-337)+(2.003), (I-337)+(2.004), (I-337)+(2.005), (I-337)+(2.006), (I-337)+(2.007), (I-337)+(2.008), (I-337)+(2.009), (I-337)+(2.010), (I-337)+(2.011), (I-337)+(2.012), (I-337)+(2.013), (I-337)+(2.014), (I-337)+(2.015), (I-337)+(2.016), (I-337)+(2.017), (I-337)+(2.018), (I-337)+(2.019), (I-337)+(2.020), (I-337)+(2.021), (I-337)+(2.022), (I-337)+(2.023), (I-337)+(2.024), (I-337)+(2.025), (I-337)+(2.026), (I-337)+(2.027), (I-337)+(2.028), (I-337)+(2.029), (I-337)+(2.030), (I-337)+(2.031), (I-337)+(2.032), (I-337)+(2.033), (I-337)+(2.034), (I-337)+(2.035), (I-337)+(2.036), (I-337)+(2.037), (I-337)+(2.038), (I-337)+(2.039), (I-337)+(2.040), (I-337)+(2.041), (I-337)+(2.042), (I-337)+(2.043), (I-337)+(2.044), (I-337)+(2.045), (I-337)+(2.046), (I-337)+(2.047), (I-337)+(2.048), (I-337)+(2.049), (I-337)+(2.050), (I-337)+(2.051), (I-337)+(2.052), (I-337)+(2.053), (I-337)+(2.054), (I-337)+(2.055), (I-337)+(2.056), (I-337)+(2.057), (I-337)+(2.058), (I-337)+(2.059), (I-337)+(2.060), (I-337)+(3.001), (I-337)+(3.002), (I-337)+(3.003), (I-337)+(3.004), (I-337)+(3.005), (I-337)+(3.006), (I-337)+(3.007), (I-337)+(3.008), (I-337)+(3.009), (I-337)+(3.010), (I-337)+(3.011), (I-337)+(3.012), (I-337)+(3.013), (I-337)+(3.014), (I-337)+(3.015), (I-337)+(3.016), (I-337)+(3.017), (I-337)+(3.018), (I-337)+(3.019), (I-337)+(3.020), (I-337)+(3.021), (I-337)+(3.022), (I-337)+(3.023), (I-337)+(3.024), (I-337)+(3.025), (I-337)+(3.026), (I-337)+(3.027), (I-337)+(3.028), (I-337)+(3.029), (I-337)+(3.030), (I-337)+(3.031), (I-337)+(3.032), (I-337)+(4.001), (I-337)+(4.002), (I-337)+(4.003), (I-337)+(4.004), (I-337)+(4.005), (I-337)+(4.006), (I-337)+(4.007), (I-337)+(4.008), (I-337)+(4.009), (I-337)+(4.010), (I-337)+(4.011), (I-337)+(4.012), (I-337)+(4.013), (I-337)+(4.014), (I-337)+(4.015), (I-337)+(4.016), (I-337)+(4.017), (I-337)+(4.018), (I-337)+(4.019), (I-337)+(4.020), (I-337)+(4.021), (I-337)+(4.022), (I-337)+(4.023), (I-337)+(4.024), (I-337)+(4.025), (I-337)+(4.026), (I-337)+(5.001), (I-337)+(5.002), (I-337)+(5.003), (I-337)+(5.004), (I-337)+(5.005), (I-337)+(5.006), (I-337)+(5.007), (I-337)+(5.008), (I-337)+(5.009), (I-337)+(5.010), (I-337)+(5.011), (I-337)+(5.012), (I-337)+(5.013), (I-337)+(5.014), (I-337)+(5.015), (I-337)+(5.016), (I-337)+(5.017), (I-337)+(5.018), (I-337)+(5.019), (I-337)+(5.020), (I-337)+(5.021), (I-337)+(5.022), (I-337)+(5.023), (I-337)+(6.001), (I-337)+(6.002), (I-337)+(6.003), (I-337)+(6.004), (I-337)+(7.001), (I-337)+(7.002), (I-337)+(7.003), (I-337)+(7.004), (I-337)+(7.005), (I-337)+(7.006), (I-337)+(8.001), (I-337)+(9.001), (I-337)+(9.002), (I-337)+(9.003), (I-337)+(9.004), (I-337)+(9.005), (I-337)+(9.006), (I-337)+(9.007), (I-337)+(9.008), (I-337)+(9.009), (I-337)+(10.001), (I-337)+(10.002), (I-337)+(10.003), (I-337)+(11.001), (I-337)+(11.002), (I-337)+(12.001), (I-337)+(12.002), (I-337)+(12.003), (I-337)+(12.004), (I-337)+(13.001), (I-337)+(13.002), (I-337)+(13.003), (I-337)+(13.004), (I-337)+(13.005), (I-337)+(13.006), (I-337)+(14.001), (I-337)+(14.002), (I-337)+(15.001), (I-337)+(15.002), (I-337)+(15.003), (I-337)+(15.004), (I-337)+(15.005), (I-337)+(15.006), (I-337)+(15.007), (I-337)+(15.008), (I-337)+(15.009), (I-337)+(15.010), (I-337)+(15.011), (I-337)+(15.012), (I-337)+(15.013), (I-337)+(15.014), (I-337)+(15.015), (I-337)+(15.016), (I-337)+(15.017), (I-337)+(15.018), (I-337)+(15.019), (I-337)+(15.020), (I-337)+(15.021), (I-337)+(15.022), (I-337)+(15.023), (I-337)+(15.024), (I-337)+(15.025), (I-337)+(15.026), (I-337)+(15.027), (I-337)+(15.028), (I-337)+(15.029), (I-337)+(15.030), (I-337)+(15.031), (I-337)+(15.032), (I-337)+(15.033), (I-337)+(15.034), (I-337)+(15.035), (I-337)+(15.036), (I-337)+(15.037), (I-337)+(15.038), (I-337)+(15.039), (I-337)+(15.040), (I-337)+(15.041), (I-337)+(15.042), (I-337)+(15.043), (I-337)+(15.044), (I-337)+(15.045), (I-337)+(15.046), (I-337)+(15.047), (I-337)+(15.048), (I-337)+(15.049), (I-337)+(15.050), (I-337)+(15.051), (I-337)+(15.052), (I-337)+(15.053), (I-337)+(15.054), (I-337)+(15.055), (I-337)+(15.056), (I-337)+(15.057), (I-337)+(15.058), (I-337)+(15.059), (I-337)+(15.060), (I-337)+(15.061), (I-337)+(15.062), (I-337)+(15.063), (I-337)+(15.064), (I-337)+(15.065), (I-337)+(15.066), (I-337)+(15.067), (I-337)+(15.068), (I-337)+(15.069), (I-337)+(15.070), (I-337)+(15.071), (I-337)+(15.072), (I-337)+(15.073), (I-337)+(15.074), (I-337)+(15.075), (I-337)+(15.076), (I-337)+(15.077), (I-337)+(15.078), (I-337)+(15.079), (I-337)+(15.080), (I-337)+(15.081), (I-337)+(15.082), (I-337)+(15.083), (I-337)+(15.084), (I-337)+(15.085), (I-337)+(15.086), (I-337)+(15.087), (I-337)+(15.088), (I-337)+(15.089), (I-337)+(15.090), (I-337)+(15.091), (I-337)+(15.092), (I-337)+(15.093), (I-337)+(15.094), (I-337)+(15.095), (I-337)+(15.096), (I-337)+(15.097), (I-337)+(15.098), (I-337)+(15.099), (I-337)+(15.100), (I-337)+(15.101), (I-337)+(15.102), (I-337)+(15.103), (I-337)+(15.104), (I-337)+(15.105), (I-337)+(15.106), (I-337)+(15.107), (I-337)+(15.108), (I-337)+(15.109), (I-337)+(15.110), (I-337)+(15.111), (I-337)+(15.112), (I-337)+(15.113), (I-337)+(15.114), (I-337)+(15.115), (I-337)+(15.116), (I-337)+(15.117), (I-337)+(15.118), (I-337)+(15.119), (I-337)+(15.120), (I-337)+(15.121), (I-337)+(15.122), (I-337)+(15.123), (I-337)+(15.124), (I-337)+(15.125), (I-337)+(15.126), (I-337)+(15.127), (I-337)+(15.128), (I-337)+(16.001), (I-337)+(16.002), (I-337)+(16.003), (I-337)+(16.004), (I-337)+(16.005), (I-337)+(16.006), (I-337)+(16.007), (I-337)+(16.008), (I-337)+(17.001), (I-337)+(17.002), (I-337)+(17.003), (I-337)+(17.004), (I-337)+(17.005), (I-337)+(17.006), (I-337)+(17.007), (I-337)+(17.008), (I-337)+(17.009), (I-337)+(17.010), (I-337)+(17.011), (I-337)+(17.012) and (I-337)+(18.001).

Also preferred compound combinations are selected from group (G5) consisting of the following mixtures:

(I-337)+(1.001), (I-337)+(1.002), (I-337)+(1.003), (I-337)+(1.004), (I-337)+(1.005), (I-337)+(1.006), (I-337)+(1.007), (I-337)+(1.008), (I-337)+(1.009), (I-337)+(1.010), (I-337)+(1.011), (I-337)+(1.012), (I-337)+(1.013), (I-337)+(1.014), (I-337)+(1.015), (I-337)+(1.016), (I-337)+(1.017), (I-337)+(1.018), (I-337)+(1.019), (I-337)+(1.020), (I-337)+(1.021), (I-337)+(1.022), (I-337)+(1.023), (I-337)+(1.024), (I-337)+(1.025), (I-337)+(1.026), (I-337)+(1.027), (I-337)+(1.028), (I-337)+(1.029), (I-337)+(1.030), (I-337)+(1.031), (I-337)+(1.032), (I-337)+(1.033), (I-337)+(1.034), (I-337)+(1.035), (I-337)+(1.036), (I-337)+(1.037), (I-337)+(1.038), (I-337)+(1.039), (I-337)+(1.040), (I-337)+(1.041), (I-337)+(1.042), (I-337)+(1.043), (I-337)+(1.044), (I-337)+(1.045), (I-337)+(1.046), (I-337)+(1.047), (I-337)+(1.048), (I-337)+(1.049), (I-337)+(1.050), (I-337)+(1.051), (I-337)+(1.052), (I-337)+(1.053), (I-337)+(1.054), (I-337)+(1.055), (I-337)+(1.056), (I-337)+(1.057), (I-337)+(1.058), (I-337)+(1.059), (I-337)+(1.060), (I-337)+(1.061), (I-337)+(1.062), (I-337)+(1.063), (I-337)+(1.064), (I-337)+(1.065), (I-337)+(1.066), (I-337)+(1.067), (I-337)+(1.068), (I-337)+(1.069), (I-337)+(1.070), (I-337)+(1.071), (I-337)+(1.072), (I-337)+(1.073), (I-337)+(1.074), (I-337)+(1.075), (I-337)+(1.076), (I-337)+(1.077), (I-337)+(1.078), (I-337)+(1.079), (I-337)+(1.080), (I-337)+(1.081), (I-337)+(1.082), (I-337)+(1.083), (I-337)+(1.084), (I-337)+(1.085), (I-337)+(1.086), (I-337)+(1.087), (I-337)+(1.088), (I-337)+(1.089), (I-337)+(1.090), (I-337)+(1.091), (I-337)+(1.092), (I-337)+(2.001), (I-337)+(2.002), (I-337)+(2.003), (I-337)+(2.004), (I-337)+(2.005), (I-337)+(2.006), (I-337)+(2.007), (I-337)+(2.008), (I-337)+(2.009), (I-337)+(2.010), (I-337)+(2.011), (I-337)+(2.012), (I-337)+(2.013), (I-337)+(2.014), (I-337)+(2.015), (I-337)+(2.016), (I-337)+(2.017), (I-337)+(2.018), (I-337)+(2.019), (I-337)+(2.020), (I-337)+(2.021), (I-337)+(2.022), (I-337)+(2.023), (I-337)+(2.024), (I-337)+(2.025), (I-337)+(2.026), (I-337)+(2.027), (I-337)+(2.028), (I-337)+(2.029), (I-337)+(2.030), (I-337)+(2.031), (I-337)+(2.032), (I-337)+(2.033), (I-337)+(2.034), (I-337)+(2.035), (I-337)+(2.036), (I-337)+(2.037), (I-337)+(2.038), (I-337)+(2.039), (I-337)+(2.040), (I-337)+(2.041), (I-337)+(2.042), (I-337)+(2.043), (I-337)+(2.044), (I-337)+(2.045), (I-337)+(2.046), (I-337)+(2.047), (I-337)+(2.048), (I-337)+(2.049), (I-337)+(2.050), (I-337)+(2.051), (I-337)+(2.052), (I-337)+(2.053), (I-337)+(2.054), (I-337)+(2.055), (I-337)+(2.056), (I-337)+(2.057), (I-337)+(2.058), (I-337)+(2.059), (I-337)+(3.001), (I-337)+(3.002), (I-337)+(3.003), (I-337)+(3.004), (I-337)+(3.005), (I-337)+(3.006), (I-337)+(3.007), (I-337)+(3.008), (I-337)+(3.009), (I-337)+(3.010), (I-337)+(3.011), (I-337)+(3.012), (I-337)+(3.013), (I-337)+(3.014), (I-337)+(3.015), (I-337)+(3.016), (I-337)+(3.017), (I-337)+(3.018), (I-337)+(3.019), (I-337)+(3.020), (I-337)+(3.021), (I-337)+(3.022), (I-337)+(3.023), (I-337)+(3.024), (I-337)+(3.025), (I-337)+(3.026), (I-337)+(3.027), (I-337)+(3.028), (I-337)+(3.029), (I-337)+(3.030), (I-337)+(3.031), (I-337)+(4.001), (I-337)+(4.002), (I-337)+(4.003), (I-337)+(4.004), (I-337)+(4.005), (I-337)+(4.006), (I-337)+(4.007), (I-337)+(4.008), (I-337)+(4.009), (I-337)+(4.010), (I-337)+(4.011), (I-337)+(4.012), (I-337)+(4.013), (I-337)+(4.014), (I-337)+(4.015), (I-337)+(4.016), (I-337)+(4.017), (I-337)+(4.018), (I-337)+(4.019), (I-337)+(4.020), (I-337)+(4.021), (I-337)+(4.022), (I-337)+(4.023), (I-337)+(4.024), (I-337)+(4.025), (I-337)+(4.026), (I-337)+(5.001), (I-337)+(5.002), (I-337)+(5.003), (I-337)+(5.004), (I-337)+(5.005), (I-337)+(5.006), (I-337)+(5.007), (I-337)+(5.008), (I-337)+(5.009), (I-337)+(5.010), (I-337)+(5.011), (I-337)+(5.012), (I-337)+(5.013), (I-337)+(5.014), (I-337)+(5.015), (I-337)+(5.016), (I-337)+(5.017), (I-337)+(5.018), (I-337)+(5.019), (I-337)+(5.020), (I-337)+(5.021), (I-337)+(5.022), (I-337)+(5.023), (I-337)+(6.001), (I-337)+(6.002), (I-337)+(6.003), (I-337)+(6.004), (I-337)+(7.001), (I-337)+(7.002), (I-337)+(7.003), (I-337)+(7.004), (I-337)+(7.005), (I-337)+(7.006), (I-337)+(8.001), (I-337)+(9.001), (I-337)+(9.002), (I-337)+(9.003), (I-337)+(9.004), (I-337)+(9.005), (I-337)+(9.006), (I-337)+(9.007), (I-337)+(9.008), (I-337)+(9.009), (I-337)+(10.001), (I-337)+(10.002), (I-337)+(10.003), (I-337)+(11.001), (I-337)+(11.002), (I-337)+(12.001), (I-337)+(12.002), (I-337)+(12.003), (I-337)+(12.004), (I-337)+(13.001), (I-337)+(13.002), (I-337)+(13.003), (I-337)+(13.004), (I-337)+(13.005), (I-337)+(13.006), (I-337)+(14.001), (I-337)+(14.002), (I-337)+(15.001), (I-337)+(15.002), (I-337)+(15.003), (I-337)+(15.004), (I-337)+(15.005), (I-337)+(15.006), (I-337)+(15.007), (I-337)+(15.008), (I-337)+(15.009), (I-337)+(15.010), (I-337)+(15.011), (I-337)+(15.012), (I-337)+(15.013), (I-337)+(15.014), (I-337)+(15.015), (I-337)+(15.016), (I-337)+(15.017), (I-337)+(15.018), (I-337)+(15.019), (I-337)+(15.020), (I-337)+(15.021), (I-337)+(15.022), (I-337)+(15.023), (I-337)+(15.024), (I-337)+(15.025), (I-337)+(15.026), (I-337)+(15.027), (I-337)+(15.028), (I-337)+(15.029), (I-337)+(15.030), (I-337)+(15.031), (I-337)+(15.032), (I-337)+(15.033), (I-337)+(15.034), (I-337)+(15.035), (I-337)+(15.036), (I-337)+(15.037), (I-337)+(15.038), (I-337)+(15.039), (I-337)+(15.040), (I-337)+(15.041), (I-337)+(15.042), (I-337)+(15.043), (I-337)+(15.044), (I-337)+(15.045), (I-337)+(15.046), (I-337)+(15.047), (I-337)+(15.048), (I-337)+(15.049), (I-337)+(15.050), (I-337)+(15.051), (I-337)+(15.052), (I-337)+(15.053), (I-337)+(15.054), (I-337)+(15.055), (I-337)+(15.056), (I-337)+(15.057), (I-337)+(15.058), (I-337)+(15.059), (I-337)+(15.060), (I-337)+(15.061), (I-337)+(15.062), (I-337)+(15.063), (I-337)+(15.064), (I-337)+(15.065), (I-337)+(15.066), (I-337)+(15.067), (I-337)+(15.068), (I-337)+(15.069), (I-337)+(15.070), (I-337)+(15.071), (I-337)+(15.072), (I-337)+(15.073), (I-337)+(15.074), (I-337)+(15.075), (I-337)+(15.076), (I-337)+(15.077), (I-337)+(15.078), (I-337)+(15.079), (I-337)+(15.080), (I-337)+(15.081), (I-337)+(15.082), (I-337)+(15.083), (I-337)+(15.084), (I-337)+(15.085), (I-337)+(15.086), (I-337)+(15.087), (I-337)+(15.088), (I-337)+(15.089), (I-337)+(15.090), (I-337)+(15.091), (I-337)+(15.092), (I-337)+(15.093), (I-337)+(15.094), (I-337)+(15.095), (I-337)+(15.096), (I-337)+(15.097), (I-337)+(15.098), (I-337)+(15.099), (I-337)+(15.100), (I-337)+(15.101), (I-337)+(15.102), (I-337)+(15.103), (I-337)+(15.104), (I-337)+(15.105), (I-337)+(15.106), (I-337)+(15.107), (I-337)+(15.108), (I-337)+(15.109), (I-337)+(15.110), (I-337)+(15.111), (I-337)+(15.112), (I-337)+(15.113), (I-337)+(15.114), (I-337)+(15.115), (I-337)+(15.116), (I-337)+(15.117), (I-337)+(15.118), (I-337)+(15.119), (I-337)+(15.120), (I-337)+(15.121), (I-337)+(15.122), (I-337)+(15.123), (I-337)+(15.124), (I-337)+(15.125), (I-337)+(15.126), (I-337)+(15.127), (I-337)+(16.001), (I-337)+(16.002), (I-337)+(16.003), (I-337)+(16.004), (I-337)+(16.005), (I-337)+(16.006), (I-337)+(16.007), (I-337)+(16.008), (I-337)+(17.001), (I-337)+(17.002), (I-337)+(17.003), (I-337)+(17.004), (I-337)+(17.005), (I-337)+(17.006), (I-337)+(17.007), (I-337)+(17.008), (I-337)+(17.009), (I-337)+(17.010), (I-337)+(17.011), (I-337)+(17.012) and (I-337)+(18.001).

Also preferred compound combinations are selected from group (G7-1) consisting of the following mixtures:

(I-338)+(1.001), (I-338)+(1.002), (I-338)+(1.003), (I-338)+(1.004), (I-338)+(1.005), (I-338)+(1.006), (I-338)+(1.007), (I-338)+(1.008), (I-338)+(1.009), (I-338)+(1.010), (I-338)+(1.011), (I-338)+(1.012), (I-338)+(1.013), (I-338)+(1.014), (I-338)+(1.015), (I-338)+(1.016), (I-338)+(1.017), (I-338)+(1.018), (I-338)+(1.019), (I-338)+(1.020), (I-338)+(1.021), (I-338)+(1.022), (I-338)+(1.023), (I-338)+(1.024), (I-338)+(1.025), (I-338)+(1.026), (I-338)+(1.027), (I-338)+(1.028), (I-338)+(1.029), (I-338)+(1.030), (I-338)+(1.031), (I-338)+(1.032), (I-338)+(1.033), (I-338)+(1.034), (I-338)+(1.035), (I-338)+(1.036), (I-338)+(1.037), (I-338)+(1.038), (I-338)+(1.039), (I-338)+(1.040), (I-338)+(1.041), (I-338)+(1.042), (I-338)+(1.043), (I-338)+(1.044), (I-338)+(1.045), (I-338)+(1.046), (I-338)+(1.047), (I-338)+(1.048), (I-338)+(1.049), (I-338)+(1.050), (I-338)+(1.051), (I-338)+(1.052), (I-338)+(1.053), (I-338)+(1.054), (I-338)+(1.055), (I-338)+(1.056), (I-338)+(1.057), (I-338)+(1.058), (I-338)+(1.059), (I-338)+(1.060), (I-338)+(1.061), (I-338)+(1.062), (I-338)+(1.063), (I-338)+(1.064), (I-338)+(1.065), (I-338)+(1.066), (I-338)+(1.067), (I-338)+(1.068), (I-338)+(1.069), (I-338)+(1.070), (I-338)+(1.071), (I-338)+(1.072), (I-338)+(1.073), (I-338)+(1.074), (I-338)+(1.075), (I-338)+(1.076), (I-338)+(1.077), (I-338)+(1.078), (I-338)+(1.079), (I-338)+(1.080), (I-338)+(1.081), (I-338)+(1.082), (I-338)+(1.083), (I-338)+(1.084), (I-338)+(1.085), (I-338)+(1.086), (I-338)+(1.087), (I-338)+(1.088), (I-338)+(1.089), (I-338)+(1.090), (I-338)+(1.091), (I-338)+(1.092), (I-338)+(2.001), (I-338)+(2.002), (I-338)+(2.003), (I-338)+(2.004), (I-338)+(2.005), (I-338)+(2.006), (I-338)+(2.007), (I-338)+(2.008), (I-338)+(2.009), (I-338)+(2.010), (I-338)+(2.011), (I-338)+(2.012), (I-338)+(2.013), (I-338)+(2.014), (I-338)+(2.015), (I-338)+(2.016), (I-338)+(2.017), (I-338)+(2.018), (I-338)+(2.019), (I-338)+(2.020), (I-338)+(2.021), (I-338)+(2.022), (I-338)+(2.023), (I-338)+(2.024), (I-338)+(2.025), (I-338)+(2.026), (I-338)+(2.027), (I-338)+(2.028), (I-338)+(2.029), (I-338)+(2.030), (I-338)+(2.031), (I-338)+(2.032), (I-338)+(2.033), (I-338)+(2.034), (I-338)+(2.035), (I-338)+(2.036), (I-338)+(2.037), (I-338)+(2.038), (I-338)+(2.039), (I-338)+(2.040), (I-338)+(2.041), (I-338)+(2.042), (I-338)+(2.043), (I-338)+(2.044), (I-338)+(2.045), (I-338)+(2.046), (I-338)+(2.047), (I-338)+(2.048), (I-338)+(2.049), (I-338)+(2.050), (I-338)+(2.051), (I-338)+(2.052), (I-338)+(2.053), (I-338)+(2.054), (I-338)+(2.055), (I-338)+(2.056), (I-338)+(2.057), (I-338)+(2.058), (I-338)+(2.059), (I-338)+(2.060), (I-338)+(3.001), (I-338)+(3.002), (I-338)+(3.003), (I-338)+(3.004), (I-338)+(3.005), (I-338)+(3.006), (I-338)+(3.007), (I-338)+(3.008), (I-338)+(3.009), (I-338)+(3.010), (I-338)+(3.011), (I-338)+(3.012), (I-338)+(3.013), (I-338)+(3.014), (I-338)+(3.015), (I-338)+(3.016), (I-338)+(3.017), (I-338)+(3.018), (I-338)+(3.019), (I-338)+(3.020), (I-338)+(3.021), (I-338)+(3.022), (I-338)+(3.023), (I-338)+(3.024), (I-338)+(3.025), (I-338)+(3.026), (I-338)+(3.027), (I-338)+(3.028), (I-338)+(3.029), (I-338)+(3.030), (I-338)+(3.031), (I-338)+(3.032), (I-338)+(4.001), (I-338)+(4.002), (I-338)+(4.003), (I-338)+(4.004), (I-338)+(4.005), (I-338)+(4.006), (I-338)+(4.007), (I-338)+(4.008), (I-338)+(4.009), (I-338)+(4.010), (I-338)+(4.011), (I-338)+(4.012), (I-338)+(4.013), (I-338)+(4.014), (I-338)+(4.015), (I-338)+(4.016), (I-338)+(4.017), (I-338)+(4.018), (I-338)+(4.019), (I-338)+(4.020), (I-338)+(4.021), (I-338)+(4.022), (I-338)+(4.023), (I-338)+(4.024), (I-338)+(4.025), (I-338)+(4.026), (I-338)+(5.001), (I-338)+(5.002), (I-338)+(5.003), (I-338)+(5.004), (I-338)+(5.005), (I-338)+(5.006), (I-338)+(5.007), (I-338)+(5.008), (I-338)+(5.009), (I-338)+(5.010), (I-338)+(5.011), (I-338)+(5.012), (I-338)+(5.013), (I-338)+(5.014), (I-338)+(5.015), (I-338)+(5.016), (I-338)+(5.017), (I-338)+(5.018), (I-338)+(5.019), (I-338)+(5.020), (I-338)+(5.021), (I-338)+(5.022), (I-338)+(5.023), (I-338)+(6.001), (I-338)+(6.002), (I-338)+(6.003), (I-338)+(6.004), (I-338)+(7.001), (I-338)+(7.002), (I-338)+(7.003), (I-338)+(7.004), (I-338)+(7.005), (I-338)+(7.006), (I-338)+(8.001), (I-338)+(9.001), (I-338)+(9.002), (I-338)+(9.003), (I-338)+(9.004), (I-338)+(9.005), (I-338)+(9.006), (I-338)+(9.007), (I-338)+(9.008), (I-338)+(9.009), (I-338)+(10.001), (I-338)+(10.002), (I-338)+(10.003), (I-338)+(11.001), (I-338)+(11.002), (I-338)+(12.001), (I-338)+(12.002), (I-338)+(12.003), (I-338)+(12.004), (I-338)+(13.001), (I-338)+(13.002), (I-338)+(13.003), (I-338)+(13.004), (I-338)+(13.005), (I-338)+(13.006), (I-338)+(14.001), (I-338)+(14.002), (I-338)+(15.001), (I-338)+(15.002), (I-338)+(15.003), (I-338)+(15.004), (I-338)+(15.005), (I-338)+(15.006), (I-338)+(15.007), (I-338)+(15.008), (I-338)+(15.009), (I-338)+(15.010), (I-338)+(15.011), (I-338)+(15.012), (I-338)+(15.013), (I-338)+(15.014), (I-338)+(15.015), (I-338)+(15.016), (I-338)+(15.017), (I-338)+(15.018), (I-338)+(15.019), (I-338)+(15.020), (I-338)+(15.021), (I-338)+(15.022), (I-338)+(15.023), (I-338)+(15.024), (I-338)+(15.025), (I-338)+(15.026), (I-338)+(15.027), (I-338)+(15.028), (I-338)+(15.029), (I-338)+(15.030), (I-338)+(15.031), (I-338)+(15.032), (I-338)+(15.033), (I-338)+(15.034), (I-338)+(15.035), (I-338)+(15.036), (I-338)+(15.037), (I-338)+(15.038), (I-338)+(15.039), (I-338)+(15.040), (I-338)+(15.041), (I-338)+(15.042), (I-338)+(15.043), (I-338)+(15.044), (I-338)+(15.045), (I-338)+(15.046), (I-338)+(15.047), (I-338)+(15.048), (I-338)+(15.049), (I-338)+(15.050), (I-338)+(15.051), (I-338)+(15.052), (I-338)+(15.053), (I-338)+(15.054), (I-338)+(15.055), (I-338)+(15.056), (I-338)+(15.057), (I-338)+(15.058), (I-338)+(15.059), (I-338)+(15.060), (I-338)+(15.061), (I-338)+(15.062), (I-338)+(15.063), (I-338)+(15.064), (I-338)+(15.065), (I-338)+(15.066), (I-338)+(15.067), (I-338)+(15.068), (I-338)+(15.069), (I-338)+(15.070), (I-338)+(15.071), (I-338)+(15.072), (I-338)+(15.073), (I-338)+(15.074), (I-338)+(15.075), (I-338)+(15.076), (I-338)+(15.077), (I-338)+(15.078), (I-338)+(15.079), (I-338)+(15.080), (I-338)+(15.081), (I-338)+(15.082), (I-338)+(15.083), (I-338)+(15.084), (I-338)+(15.085), (I-338)+(15.086), (I-338)+(15.087), (I-338)+(15.088), (I-338)+(15.089), (I-338)+(15.090), (I-338)+(15.091), (I-338)+(15.092), (I-338)+(15.093), (I-338)+(15.094), (I-338)+(15.095), (I-338)+(15.096), (I-338)+(15.097), (I-338)+(15.098), (I-338)+(15.099), (I-338)+(15.100), (I-338)+(15.101), (I-338)+(15.102), (I-338)+(15.103), (I-338)+(15.104), (I-338)+(15.105), (I-338)+(15.106), (I-338)+(15.107), (I-338)+(15.108), (I-338)+(15.109), (I-338)+(15.110), (I-338)+(15.111), (I-338)+(15.112), (I-338)+(15.113), (I-338)+(15.114), (I-338)+(15.115), (I-338)+(15.116), (I-338)+(15.117), (I-338)+(15.118), (I-338)+(15.119), (I-338)+(15.120), (I-338)+(15.121), (I-338)+(15.122), (I-338)+(15.123), (I-338)+(15.124), (I-338)+(15.125), (I-338)+(15.126), (I-338)+(15.127), (I-338)+(15.128), (I-338)+(16.001), (I-338)+(16.002), (I-338)+(16.003), (I-338)+(16.004), (I-338)+(16.005), (I-338)+(16.006), (I-338)+(16.007), (I-338)+(16.008), (I-338)+(17.001), (I-338)+(17.002), (I-338)+(17.003), (I-338)+(17.004), (I-338)+(17.005), (I-338)+(17.006), (I-338)+(17.007), (I-338)+(17.008), (I-338)+(17.009), (I-338)+(17.010), (I-338)+(17.011), (I-338)+(17.012) and (I-338)+(18.001).

Also preferred compound combinations are selected from group (G6-1) consisting of the following mixtures:

(I-339)+(1.001), (I-339)+(1.002), (I-339)+(1.003), (I-339)+(1.004), (I-339)+(1.005), (I-339)+(1.006), (I-339)+(1.007), (I-339)+(1.008), (I-339)+(1.009), (I-339)+(1.010), (I-339)+(1.011), (I-339)+(1.012), (I-339)+(1.013), (I-339)+(1.014), (I-339)+(1.015), (I-339)+(1.016), (I-339)+(1.017), (I-339)+(1.018), (I-339)+(1.019), (I-339)+(1.020), (I-339)+(1.021), (I-339)+(1.022), (I-339)+(1.023), (I-339)+(1.024), (I-339)+(1.025), (I-339)+(1.026), (I-339)+(1.027), (I-339)+(1.028), (I-339)+(1.029), (I-339)+(1.030), (I-339)+(1.031), (I-339)+(1.032), (I-339)+(1.033), (I-339)+(1.034), (I-339)+(1.035), (I-339)+(1.036), (I-339)+(1.037), (I-339)+(1.038), (I-339)+(1.039), (I-339)+(1.040), (I-339)+(1.041), (I-339)+(1.042), (I-339)+(1.043), (I-339)+(1.044), (I-339)+(1.045), (I-339)+(1.046), (I-339)+(1.047), (I-339)+(1.048), (I-339)+(1.049), (I-339)+(1.050), (I-339)+(1.051), (I-339)+(1.052), (I-339)+(1.053), (I-339)+(1.054), (I-339)+(1.055), (I-339)+(1.056), (I-339)+(1.057), (I-339)+(1.058), (I-339)+(1.059), (I-339)+(1.060), (I-339)+(1.061), (I-339)+(1.062), (I-339)+(1.063), (I-339)+(1.064), (I-339)+(1.065), (I-339)+(1.066), (I-339)+(1.067), (I-339)+(1.068), (I-339)+(1.069), (I-339)+(1.070), (I-339)+(1.071), (I-339)+(1.072), (I-339)+(1.073), (I-339)+(1.074), (I-339)+(1.075), (I-339)+(1.076), (I-339)+(1.077), (I-339)+(1.078), (I-339)+(1.079), (I-339)+(1.080), (I-339)+(1.081), (I-339)+(1.082), (I-339)+(1.083), (I-339)+(1.084), (I-339)+(1.085), (I-339)+(1.086), (I-339)+(1.087), (I-339)+(1.088), (I-339)+(1.089), (I-339)+(1.090), (I-339)+(1.091), (I-339)+(1.092), (I-339)+(2.001), (I-339)+(2.002), (I-339)+(2.003), (I-339)+(2.004), (I-339)+(2.005), (I-339)+(2.006), (I-339)+(2.007), (I-339)+(2.008), (I-339)+(2.009), (I-339)+(2.010), (I-339)+(2.011), (I-339)+(2.012), (I-339)+(2.013), (I-339)+(2.014), (I-339)+(2.015), (I-339)+(2.016), (I-339)+(2.017), (I-339)+(2.018), (I-339)+(2.019), (I-339)+(2.020), (I-339)+(2.021), (I-339)+(2.022), (I-339)+(2.023), (I-339)+(2.024), (I-339)+(2.025), (I-339)+(2.026), (I-339)+(2.027), (I-339)+(2.028), (I-339)+(2.029), (I-339)+(2.030), (I-339)+(2.031), (I-339)+(2.032), (I-339)+(2.033), (I-339)+(2.034), (I-339)+(2.035), (I-339)+(2.036), (I-339)+(2.037), (I-339)+(2.038), (I-339)+(2.039), (I-339)+(2.040), (I-339)+(2.041), (I-339)+(2.042), (I-339)+(2.043), (I-339)+(2.044), (I-339)+(2.045), (I-339)+(2.046), (I-339)+(2.047), (I-339)+(2.048), (I-339)+(2.049), (I-339)+(2.050), (I-339)+(2.051), (I-339)+(2.052), (I-339)+(2.053), (I-339)+(2.054), (I-339)+(2.055), (I-339)+(2.056), (I-339)+(2.057), (I-339)+(2.058), (I-339)+(2.059), (I-339)+(2.060), (I-339)+(3.001), (I-339)+(3.002), (I-339)+(3.003), (I-339)+(3.004), (I-339)+(3.005), (I-339)+(3.006), (I-339)+(3.007), (I-339)+(3.008), (I-339)+(3.009), (I-339)+(3.010), (I-339)+(3.011), (I-339)+(3.012), (I-339)+(3.013), (I-339)+(3.014), (I-339)+(3.015), (I-339)+(3.016), (I-339)+(3.017), (I-339)+(3.018), (I-339)+(3.019), (I-339)+(3.020), (I-339)+(3.021), (I-339)+(3.022), (I-339)+(3.023), (I-339)+(3.024), (I-339)+(3.025), (I-339)+(3.026), (I-339)+(3.027), (I-339)+(3.028), (I-339)+(3.029), (I-339)+(3.030), (I-339)+(3.031), (I-339)+(3.032), (I-339)+(4.001), (I-339)+(4.002), (I-339)+(4.003), (I-339)+(4.004), (I-339)+(4.005), (I-339)+(4.006), (I-339)+(4.007), (I-339)+(4.008), (I-339)+(4.009), (I-339)+(4.010), (I-339)+(4.011), (I-339)+(4.012), (I-339)+(4.013), (I-339)+(4.014), (I-339)+(4.015), (I-339)+(4.016), (I-339)+(4.017), (I-339)+(4.018), (I-339)+(4.019), (I-339)+(4.020), (I-339)+(4.021), (I-339)+(4.022), (I-339)+(4.023), (I-339)+(4.024), (I-339)+(4.025), (I-339)+(4.026), (I-339)+(5.001), (I-339)+(5.002), (I-339)+(5.003), (I-339)+(5.004), (I-339)+(5.005), (I-339)+(5.006), (I-339)+(5.007), (I-339)+(5.008), (I-339)+(5.009), (I-339)+(5.010), (I-339)+(5.011), (I-339)+(5.012), (I-339)+(5.013), (I-339)+(5.014), (I-339)+(5.015), (I-339)+(5.016), (I-339)+(5.017), (I-339)+(5.018), (I-339)+(5.019), (I-339)+(5.020), (I-339)+(5.021), (I-339)+(5.022), (I-339)+(5.023), (I-339)+(6.001), (I-339)+(6.002), (I-339)+(6.003), (I-339)+(6.004), (I-339)+(7.001), (I-339)+(7.002), (I-339)+(7.003), (I-339)+(7.004), (I-339)+(7.005), (I-339)+(7.006), (I-339)+(8.001), (I-339)+(9.001), (I-339)+(9.002), (I-339)+(9.003), (I-339)+(9.004), (I-339)+(9.005), (I-339)+(9.006), (I-339)+(9.007), (I-339)+(9.008), (I-339)+(9.009), (I-339)+(10.001), (I-339)+(10.002), (I-339)+(10.003), (I-339)+(11.001), (I-339)+(11.002), (I-339)+(12.001), (I-339)+(12.002), (I-339)+(12.003), (I-339)+(12.004), (I-339)+(13.001), (I-339)+(13.002), (I-339)+(13.003), (I-339)+(13.004), (I-339)+(13.005), (I-339)+(13.006), (I-339)+(14.001), (I-339)+(14.002), (I-339)+(15.001), (I-339)+(15.002), (I-339)+(15.003), (I-339)+(15.004), (I-339)+(15.005), (I-339)+(15.006), (I-339)+(15.007), (I-339)+(15.008), (I-339)+(15.009), (I-339)+(15.010), (I-339)+(15.011), (I-339)+(15.012), (I-339)+(15.013), (I-339)+(15.014), (I-339)+(15.015), (I-339)+(15.016), (I-339)+(15.017), (I-339)+(15.018), (I-339)+(15.019), (I-339)+(15.020), (I-339)+(15.021), (I-339)+(15.022), (I-339)+(15.023), (I-339)+(15.024), (I-339)+(15.025), (I-339)+(15.026), (I-339)+(15.027), (I-339)+(15.028), (I-339)+(15.029), (I-339)+(15.030), (I-339)+(15.031), (I-339)+(15.032), (I-339)+(15.033), (I-339)+(15.034), (I-339)+(15.035), (I-339)+(15.036), (I-339)+(15.037), (I-339)+(15.038), (I-339)+(15.039), (I-339)+(15.040), (I-339)+(15.041), (I-339)+(15.042), (I-339)+(15.043), (I-339)+(15.044), (I-339)+(15.045), (I-339)+(15.046), (I-339)+(15.047), (I-339)+(15.048), (I-339)+(15.049), (I-339)+(15.050), (I-339)+(15.051), (I-339)+(15.052), (I-339)+(15.053), (I-339)+(15.054), (I-339)+(15.055), (I-339)+(15.056), (I-339)+(15.057), (I-339)+(15.058), (I-339)+(15.059), (I-339)+(15.060), (I-339)+(15.061), (I-339)+(15.062), (I-339)+(15.063), (I-339)+(15.064), (I-339)+(15.065), (I-339)+(15.066), (I-339)+(15.067), (I-339)+(15.068), (I-339)+(15.069), (I-339)+(15.070), (I-339)+(15.071), (I-339)+(15.072), (I-339)+(15.073), (I-339)+(15.074), (I-339)+(15.075), (I-339)+(15.076), (I-339)+(15.077), (I-339)+(15.078), (I-339)+(15.079), (I-339)+(15.080), (I-339)+(15.081), (I-339)+(15.082), (I-339)+(15.083), (I-339)+(15.084), (I-339)+(15.085), (I-339)+(15.086), (I-339)+(15.087), (I-339)+(15.088), (I-339)+(15.089), (I-339)+(15.090), (I-339)+(15.091), (I-339)+(15.092), (I-339)+(15.093), (I-339)+(15.094), (I-339)+(15.095), (I-339)+(15.096), (I-339)+(15.097), (I-339)+(15.098), (I-339)+(15.099), (I-339)+(15.100), (I-339)+(15.101), (I-339)+(15.102), (I-339)+(15.103), (I-339)+(15.104), (I-339)+(15.105), (I-339)+(15.106), (I-339)+(15.107), (I-339)+(15.108), (I-339)+(15.109), (I-339)+(15.110), (I-339)+(15.111), (I-339)+(15.112), (I-339)+(15.113), (I-339)+(15.114), (I-339)+(15.115), (I-339)+(15.116), (I-339)+(15.117), (I-339)+(15.118), (I-339)+(15.119), (I-339)+(15.120), (I-339)+(15.121), (I-339)+(15.122), (I-339)+(15.123), (I-339)+(15.124), (I-339)+(15.125), (I-339)+(15.126), (I-339)+(15.127), (I-339)+(15.128), (I-339)+(16.001), (I-339)+(16.002), (I-339)+(16.003), (I-339)+(16.004), (I-339)+(16.005), (I-339)+(16.006), (I-339)+(16.007), (I-339)+(16.008), (I-339)+(17.001), (I-339)+(17.002), (I-339)+(17.003), (I-339)+(17.004), (I-339)+(17.005), (I-339)+(17.006), (I-339)+(17.007), (I-339)+(17.008), (I-339)+(17.009), (I-339)+(17.010), (I-339)+(17.011), (I-339)+(17.012) and (I-339)+(18.001).

Also preferred compound combinations are selected from group (G6) consisting of the following mixtures:

(I-339)+(1.001), (I-339)+(1.002), (I-339)+(1.003), (I-339)+(1.004), (I-339)+(1.005), (I-339)+(1.006), (I-339)+(1.007), (I-339)+(1.008), (I-339)+(1.009), (I-339)+(1.010), (I-339)+(1.011), (I-339)+(1.012), (I-339)+(1.013), (I-339)+(1.014), (I-339)+(1.015), (I-339)+(1.016), (I-339)+(1.017), (I-339)+(1.018), (I-339)+(1.019), (I-339)+(1.020), (I-339)+(1.021), (I-339)+(1.022), (I-339)+(1.023), (I-339)+(1.024), (I-339)+(1.025), (I-339)+(1.026), (I-339)+(1.027), (I-339)+(1.028), (I-339)+(1.029), (I-339)+(1.030), (I-339)+(1.031), (I-339)+(1.032), (I-339)+(1.033), (I-339)+(1.034), (I-339)+(1.035), (I-339)+(1.036), (I-339)+(1.037), (I-339)+(1.038), (I-339)+(1.039), (I-339)+(1.040), (I-339)+(1.041), (I-339)+(1.042), (I-339)+(1.043), (I-339)+(1.044), (I-339)+(1.045), (I-339)+(1.046), (I-339)+(1.047), (I-339)+(1.048), (I-339)+(1.049), (I-339)+(1.050), (I-339)+(1.051), (I-339)+(1.052), (I-339)+(1.053), (I-339)+(1.054), (I-339)+(1.055), (I-339)+(1.056), (I-339)+(1.057), (I-339)+(1.058), (I-339)+(1.059), (I-339)+(1.060), (I-339)+(1.061), (I-339)+(1.062), (I-339)+(1.063), (I-339)+(1.064), (I-339)+(1.065), (I-339)+(1.066), (I-339)+(1.067), (I-339)+(1.068), (I-339)+(1.069), (I-339)+(1.070), (I-339)+(1.071), (I-339)+(1.072), (I-339)+(1.073), (I-339)+(1.074), (I-339)+(1.075), (I-339)+(1.076), (I-339)+(1.077), (I-339)+(1.078), (I-339)+(1.079), (I-339)+(1.080), (I-339)+(1.081), (I-339)+(1.082), (I-339)+(1.083), (I-339)+(1.084), (I-339)+(1.085), (I-339)+(1.086), (I-339)+(1.087), (I-339)+(1.088), (I-339)+(1.089), (I-339)+(1.090), (I-339)+(1.091), (I-339)+(1.092), (I-339)+(2.001), (I-339)+(2.002), (I-339)+(2.003), (I-339)+(2.004), (I-339)+(2.005), (I-339)+(2.006), (I-339)+(2.007), (I-339)+(2.008), (I-339)+(2.009), (I-339)+(2.010), (I-339)+(2.011), (I-339)+(2.012), (I-339)+(2.013), (I-339)+(2.014), (I-339)+(2.015), (I-339)+(2.016), (I-339)+(2.017), (I-339)+(2.018), (I-339)+(2.019), (I-339)+(2.020), (I-339)+(2.021), (I-339)+(2.022), (I-339)+(2.023), (I-339)+(2.024), (I-339)+(2.025), (I-339)+(2.026), (I-339)+(2.027), (I-339)+(2.028), (I-339)+(2.029), (I-339)+(2.030), (I-339)+(2.031), (I-339)+(2.032), (I-339)+(2.033), (I-339)+(2.034), (I-339)+(2.035), (I-339)+(2.036), (I-339)+(2.037), (I-339)+(2.038), (I-339)+(2.039), (I-339)+(2.040), (I-339)+(2.041), (I-339)+(2.042), (I-339)+(2.043), (I-339)+(2.044), (I-339)+(2.045), (I-339)+(2.046), (I-339)+(2.047), (I-339)+(2.048), (I-339)+(2.049), (I-339)+(2.050), (I-339)+(2.051), (I-339)+(2.052), (I-339)+(2.053), (I-339)+(2.054), (I-339)+(2.055), (I-339)+(2.056), (I-339)+(2.057), (I-339)+(2.058), (I-339)+(2.059), (I-339)+(3.001), (I-339)+(3.002), (I-339)+(3.003), (I-339)+(3.004), (I-339)+(3.005), (I-339)+(3.006), (I-339)+(3.007), (I-339)+(3.008), (I-339)+(3.009), (I-339)+(3.010), (I-339)+(3.011), (I-339)+(3.012), (I-339)+(3.013), (I-339)+(3.014), (I-339)+(3.015), (I-339)+(3.016), (I-339)+(3.017), (I-339)+(3.018), (I-339)+(3.019), (I-339)+(3.020), (I-339)+(3.021), (I-339)+(3.022), (I-339)+(3.023), (I-339)+(3.024), (I-339)+(3.025), (I-339)+(3.026), (I-339)+(3.027), (I-339)+(3.028), (I-339)+(3.029), (I-339)+(3.030), (I-339)+(3.031), (I-339)+(4.001), (I-339)+(4.002), (I-339)+(4.003), (I-339)+(4.004), (I-339)+(4.005), (I-339)+(4.006), (I-339)+(4.007), (I-339)+(4.008), (I-339)+(4.009), (I-339)+(4.010), (I-339)+(4.011), (I-339)+(4.012), (I-339)+(4.013), (I-339)+(4.014), (I-339)+(4.015), (I-339)+(4.016), (I-339)+(4.017), (I-339)+(4.018), (I-339)+(4.019), (I-339)+(4.020), (I-339)+(4.021), (I-339)+(4.022), (I-339)+(4.023), (I-339)+(4.024), (I-339)+(4.025), (I-339)+(4.026), (I-339)+(5.001), (I-339)+(5.002), (I-339)+(5.003), (I-339)+(5.004), (I-339)+(5.005), (I-339)+(5.006), (I-339)+(5.007), (I-339)+(5.008), (I-339)+(5.009), (I-339)+(5.010), (I-339)+(5.011), (I-339)+(5.012), (I-339)+(5.013), (I-339)+(5.014), (I-339)+(5.015), (I-339)+(5.016), (I-339)+(5.017), (I-339)+(5.018), (I-339)+(5.019), (I-339)+(5.020), (I-339)+(5.021), (I-339)+(5.022), (I-339)+(5.023), (I-339)+(6.001), (I-339)+(6.002), (I-339)+(6.003), (I-339)+(6.004), (I-339)+(7.001), (I-339)+(7.002), (I-339)+(7.003), (I-339)+(7.004), (I-339)+(7.005), (I-339)+(7.006), (I-339)+(8.001), (I-339)+(9.001), (I-339)+(9.002), (I-339)+(9.003), (I-339)+(9.004), (I-339)+(9.005), (I-339)+(9.006), (I-339)+(9.007), (I-339)+(9.008), (I-339)+(9.009), (I-339)+(10.001), (I-339)+(10.002), (I-339)+(10.003), (I-339)+(11.001), (I-339)+(11.002), (I-339)+(12.001), (I-339)+(12.002), (I-339)+(12.003), (I-339)+(12.004), (I-339)+(13.001), (I-339)+(13.002), (I-339)+(13.003), (I-339)+(13.004), (I-339)+(13.005), (I-339)+(13.006), (I-339)+(14.001), (I-339)+(14.002), (I-339)+(15.001), (I-339)+(15.002), (I-339)+(15.003), (I-339)+(15.004), (I-339)+(15.005), (I-339)+(15.006), (I-339)+(15.007), (I-339)+(15.008), (I-339)+(15.009), (I-339)+(15.010), (I-339)+(15.011), (I-339)+(15.012), (I-339)+(15.013), (I-339)+(15.014), (I-339)+(15.015), (I-339)+(15.016), (I-339)+(15.017), (I-339)+(15.018), (I-339)+(15.019), (I-339)+(15.020), (I-339)+(15.021), (I-339)+(15.022), (I-339)+(15.023), (I-339)+(15.024), (I-339)+(15.025), (I-339)+(15.026), (I-339)+(15.027), (I-339)+(15.028), (I-339)+(15.029), (I-339)+(15.030), (I-339)+(15.031), (I-339)+(15.032), (I-339)+(15.033), (I-339)+(15.034), (I-339)+(15.035), (I-339)+(15.036), (I-339)+(15.037), (I-339)+(15.038), (I-339)+(15.039), (I-339)+(15.040), (I-339)+(15.041), (I-339)+(15.042), (I-339)+(15.043), (I-339)+(15.044), (I-339)+(15.045), (I-339)+(15.046), (I-339)+(15.047), (I-339)+(15.048), (I-339)+(15.049), (I-339)+(15.050), (I-339)+(15.051), (I-339)+(15.052), (I-339)+(15.053), (I-339)+(15.054), (I-339)+(15.055), (I-339)+(15.056), (I-339)+(15.057), (I-339)+(15.058), (I-339)+(15.059), (I-339)+(15.060), (I-339)+(15.061), (I-339)+(15.062), (I-339)+(15.063), (I-339)+(15.064), (I-339)+(15.065), (I-339)+(15.066), (I-339)+(15.067), (I-339)+(15.068), (I-339)+(15.069), (I-339)+(15.070), (I-339)+(15.071), (I-339)+(15.072), (I-339)+(15.073), (I-339)+(15.074), (I-339)+(15.075), (I-339)+(15.076), (I-339)+(15.077), (I-339)+(15.078), (I-339)+(15.079), (I-339)+(15.080), (I-339)+(15.081), (I-339)+(15.082), (I-339)+(15.083), (I-339)+(15.084), (I-339)+(15.085), (I-339)+(15.086), (I-339)+(15.087), (I-339)+(15.088), (I-339)+(15.089), (I-339)+(15.090), (I-339)+(15.091), (I-339)+(15.092), (I-339)+(15.093), (I-339)+(15.094), (I-339)+(15.095), (I-339)+(15.096), (I-339)+(15.097), (I-339)+(15.098), (I-339)+(15.099), (I-339)+(15.100), (I-339)+(15.101), (I-339)+(15.102), (I-339)+(15.103), (I-339)+(15.104), (I-339)+(15.105), (I-339)+(15.106), (I-339)+(15.107), (I-339)+(15.108), (I-339)+(15.109), (I-339)+(15.110), (I-339)+(15.111), (I-339)+(15.112), (I-339)+(15.113), (I-339)+(15.114), (I-339)+(15.115), (I-339)+(15.116), (I-339)+(15.117), (I-339)+(15.118), (I-339)+(15.119), (I-339)+(15.120), (I-339)+(15.121), (I-339)+(15.122), (I-339)+(15.123), (I-339)+(15.124), (I-339)+(15.125), (I-339)+(15.126), (I-339)+(15.127), (I-339)+(16.001), (I-339)+(16.002), (I-339)+(16.003), (I-339)+(16.004), (I-339)+(16.005), (I-339)+(16.006), (I-339)+(16.007), (I-339)+(16.008), (I-339)+(17.001), (I-339)+(17.002), (I-339)+(17.003), (I-339)+(17.004), (I-339)+(17.005), (I-339)+(17.006), (I-339)+(17.007), (I-339)+(17.008), (I-339)+(17.009), (I-339)+(17.010), (I-339)+(17.011), (I-339)+(17.012) and (I-339)+(18.001).

More preferred the compound combinations are selected from the mixtures belonging to groups (G1-1), (G2-1), (G3-1), (G4-1), (G6-1) and (G7-1).

More preferred the compound combinations are selected from the mixtures belonging to groups (G1), (G3) and (G4).

Even more preferred compound combinations are selected from the group (G1-1A) consisting of the following mixtures:

(I-052)+(1.002), (I-052)+(1.004), (I-052)+(1.010), (I-052)+(1.012), (I-052)+(1.018), (I-052)+(1.020), (I-052)+(1.021), (I-052)+(1.026), (I-052)+(1.027), (I-052)+(1.055), (I-052)+(1.059), (I-052)+(1.062), (I-052)+(1.067), (I-052)+(1.081), (I-052)+(1.082), (I-052)+(1.092), (I-052)+(2.001), (I-052)+(2.002), (I-052)+(2.003), (I-052)+(2.005), (I-052)+(2.007), (I-052)+(2.017), (I-052)+(2.018), (I-052)+(2.019), (I-052)+(2.021), (I-052)+(2.028), (I-052)+(2.030), (I-052)+(2.038), (I-052)+(3.003), (I-052)+(3.012), (I-052)+(3.016), (I-052)+(3.017), (I-052)+(3.020), (I-052)+(3.025), (I-052)+(3.026), (I-052)+(3.030), (I-052)+(3.031), (I-052)+(4.005), (I-052)+(4.007), (I-052)+(4.012), (I-052)+(4.015), (I-052)+(4.025), (I-052)+(5.003), (I-052)+(5.004), (I-052)+(5.010), (I-052)+(5.012), (I-052)+(5.013), (I-052)+(5.015), (I-052)+(5.018), (I-052)+(6.002), (I-052)+(7.005), (I-052)+(9.004), (I-052)+(12.003), (I-052)+(12.004), (I-052)+(13.001), (I-052)+(13.004), (I-052)+(13.005), (I-052)+(14.001), (I-052)+(14.002), (I-052)+(15.008), (I-052)+(15.012), (I-052)+(15.016), (I-052)+(15.027), (I-052)+(15.043), (I-052)+(15.047), (I-052)+(15.048), (I-052)+(15.052), (I-052)+(15.062), (I-052)+(15.064), (I-052)+(16.001), (I-052)+(17.001), (I-052)+(17.012) and (I-052)+(18.001).

Even more preferred compound combinations are selected from the group (G1-A) consisting of the following mixtures:

(I-052)+(1.002), (I-052)+(1.004), (I-052)+(1.010), (I-052)+(1.012), (I-052)+(1.018), (I-052)+(1.020), (I-052)+(1.021), (I-052)+(1.026), (I-052)+(1.027), (I-052)+(1.055), (I-052)+(1.059), (I-052)+(1.081), (I-052)+(1.082), (I-052)+(1.092), (I-052)+(2.001), (I-052)+(2.002), (I-052)+(2.003), (I-052)+(2.005), (I-052)+(2.007), (I-052)+(2.017), (I-052)+(2.018), (I-052)+(2.019), (I-052)+(2.021), (I-052)+(2.028), (I-052)+(2.030), (I-052)+(2.038), (I-052)+(3.003), (I-052)+(3.012), (I-052)+(3.016), (I-052)+(3.017), (I-052)+(3.020), (I-052)+(3.025), (I-052)+(3.026), (I-052)+(3.030), (I-052)+(3.031), (I-052)+(4.005), (I-052)+(4.007), (I-052)+(4.012), (I-052)+(4.015), (I-052)+(4.025), (I-052)+(5.003), (I-052)+(5.004), (I-052)+(5.010), (I-052)+(5.012), (I-052)+(5.013), (I-052)+(5.015), (I-052)+(5.018), (I-052)+(6.002), (I-052)+(7.005), (I-052)+(9.004), (I-052)+(12.003), (I-052)+(12.004), (I-052)+(13.001), (I-052)+(13.004), (I-052)+(13.005), (I-052)+(14.001), (I-052)+(14.002), (I-052)+(15.008), (I-052)+(15.012), (I-052)+(15.016), (I-052)+(15.027), (I-052)+(15.047), (I-052)+(15.048), (I-052)+(15.052), (I-052)+(15.062), (I-052)+(15.064), (I-052)+(16.001), (I-052)+(17.001), (I-052)+(17.012) and (I-052)+(18.001).

Even more preferred compound combinations are selected from the group (G2-1A) consisting of the following mixtures:

(I-130)+(1.002), (I-130)+(1.004), (I-130)+(1.010), (I-130)+(1.012), (I-130)+(1.018), (I-130)+(1.020), (I-130)+(1.021), (I-130)+(1.026), (I-130)+(1.027), (I-130)+(1.055), (I-130)+(1.059), (I-130)+(1.062), (I-130)+(1.067), (I-130)+(1.081), (I-130)+(1.082), (I-130)+(1.092), (I-130)+(2.001), (I-130)+(2.002), (I-130)+(2.003), (I-130)+(2.005), (I-130)+(2.007), (I-130)+(2.017), (I-130)+(2.018), (I-130)+(2.019), (I-130)+(2.021), (I-130)+(2.028), (I-130)+(2.030), (I-130)+(2.038), (I-130)+(3.003), (I-130)+(3.012), (I-130)+(3.016), (I-130)+(3.017), (I-130)+(3.020), (I-130)+(3.025), (I-130)+(3.026), (I-130)+(3.030), (I-130)+(3.031), (I-130)+(4.005), (I-130)+(4.007), (I-130)+(4.012), (I-130)+(4.015), (I-130)+(4.025), (I-130)+(5.003), (I-130)+(5.004), (I-130)+(5.010), (I-130)+(5.012), (I-130)+(5.013), (I-130)+(5.015), (I-130)+(5.018), (I-130)+(6.002), (I-130)+(7.005), (I-130)+(9.004), (I-130)+(12.003), (I-130)+(12.004), (I-130)+(13.001), (I-130)+(13.004), (I-130)+(13.005), (I-130)+(14.001), (I-130)+(14.002), (I-130)+(15.008), (I-130)+(15.012), (I-130)+(15.016), (I-130)+(15.027), (I-130)+(15.043), (I-130)+(15.047), (I-130)+(15.048), (I-130)+(15.052), (I-130)+(15.062), (I-130)+(15.064), (I-130)+(16.001), (I-130)+(17.001), (I-130)+(17.012) and (I-130)+(18.001).

Even more preferred compound combinations are also selected from the group (G3-1A) consisting of the following mixtures:

(I-300)+(1.002), (I-300)+(1.004), (I-300)+(1.010), (I-300)+(1.012), (I-300)+(1.018), (I-300)+(1.020), (I-300)+(1.021), (I-300)+(1.026), (I-300)+(1.027), (I-300)+(1.055), (I-300)+(1.059), (I-300)+(1.062), (I-300)+(1.067), (I-300)+(1.081), (I-300)+(1.082), (I-300)+(1.092), (I-300)+(2.001), (I-300)+(2.002), (I-300)+(2.003), (I-300)+(2.005), (I-300)+(2.007), (I-300)+(2.017), (I-300)+(2.018), (I-300)+(2.019), (I-300)+(2.021), (I-300)+(2.028), (I-300)+(2.030), (I-300)+(2.038), (I-300)+(3.003), (I-300)+(3.012), (I-300)+(3.016), (I-300)+(3.017), (I-300)+(3.020), (I-300)+(3.025), (I-300)+(3.026), (I-300)+(3.030), (I-300)+(3.031), (I-300)+(4.005), (I-300)+(4.007), (I-300)+(4.012), (I-300)+(4.015), (I-300)+(4.025), (I-300)+(5.003), (I-300)+(5.004), (I-300)+(5.010), (I-300)+(5.012), (I-300)+(5.013), (I-300)+(5.015), (I-300)+(5.018), (I-300)+(6.002), (I-300)+(7.005), (I-300)+(9.004), (I-300)+(12.003), (I-300)+(12.004), (I-300)+(13.001), (I-300)+(13.004), (I-300)+(13.005), (I-300)+(14.001), (I-300)+(14.002), (I-300)+(15.008), (I-300)+(15.012), (I-300)+(15.016), (I-300)+(15.027), (I-300)+(15.043), (I-300)+(15.047), (I-300)+(15.048), (I-300)+(15.052), (I-300)+(15.062), (I-300)+(15.064), (I-300)+(16.001), (I-300)+(17.001), (I-300)+(17.012) and (I-300)+(18.001).

Even more preferred compound combinations are also selected from the group (G3-A) consisting of the following mixtures:

(I-300)+(1.002), (I-300)+(1.004), (I-300)+(1.010), (I-300)+(1.012), (I-300)+(1.018), (I-300)+(1.020), (I-300)+(1.021), (I-300)+(1.026), (I-300)+(1.027), (I-300)+(1.055), (I-300)+(1.059), (I-300)+(1.081), (I-300)+(1.082), (I-300)+(1.092), (I-300)+(2.001), (I-300)+(2.002), (I-300)+(2.003), (I-300)+(2.005), (I-300)+(2.007), (I-300)+(2.017), (I-300)+(2.018), (I-300)+(2.019), (I-300)+(2.021), (I-300)+(2.028), (I-300)+(2.030), (I-300)+(2.038), (I-300)+(3.003), (I-300)+(3.012), (I-300)+(3.016), (I-300)+(3.017), (I-300)+(3.020), (I-300)+(3.025), (I-300)+(3.026), (I-300)+(3.030), (I-300)+(3.031), (I-300)+(4.005), (I-300)+(4.007), (I-300)+(4.012), (I-300)+(4.015), (I-300)+(4.025), (I-300)+(5.003), (I-300)+(5.004), (I-300)+(5.010), (I-300)+(5.012), (I-300)+(5.013), (I-300)+(5.015), (I-300)+(5.018), (I-300)+(6.002), (I-300)+(7.005), (I-300)+(9.004), (I-300)+(12.003), (I-300)+(12.004), (I-300)+(13.001), (I-300)+(13.004), (I-300)+(13.005), (I-300)+(14.001), (I-300)+(14.002), (I-300)+(15.008), (I-300)+(15.012), (I-300)+(15.016), (I-300)+(15.027), (I-300)+(15.047), (I-300)+(15.048), (I-300)+(15.052), (I-300)+(15.062), (I-300)+(15.064), (I-300)+(16.001), (I-300)+(17.001), (I-300)+(17.012) and (I-300)+(18.001).

Even more preferred compound combinations are also selected from the group (G4-1A) consisting of the following mixtures:

(I-302)+(1.002), (I-302)+(1.004), (I-302)+(1.010), (I-302)+(1.012), (I-302)+(1.018), (I-302)+(1.020), (I-302)+(1.021), (I-302)+(1.026), (I-302)+(1.027), (I-302)+(1.055), (I-302)+(1.059), (I-302)+(1.062), (I-302)+(1.067), (I-302)+(1.081), (I-302)+(1.082), (I-302)+(1.092), (I-302)+(2.001), (I-302)+(2.002), (I-302)+(2.003), (I-302)+(2.005), (I-302)+(2.007), (I-302)+(2.017), (I-302)+(2.018), (I-302)+(2.019), (I-302)+(2.021), (I-302)+(2.028), (I-302)+(2.030), (I-302)+(2.038), (I-302)+(3.003), (I-302)+(3.012), (I-302)+(3.016), (I-302)+(3.017), (I-302)+(3.020), (I-302)+(3.025), (I-302)+(3.026), (I-302)+(3.030), (I-302)+(3.031), (I-302)+(4.005), (I-302)+(4.007), (I-302)+(4.012), (I-302)+(4.015), (I-302)+(4.025), (I-302)+(5.003), (I-302)+(5.004), (I-302)+(5.010), (I-302)+(5.012), (I-302)+(5.013), (I-302)+(5.015), (I-302)+(5.018), (I-302)+(6.002), (I-302)+(7.005), (I-302)+(9.004), (I-302)+(12.003), (I-302)+(12.004), (I-302)+(13.001), (I-302)+(13.004), (I-302)+(13.005), (I-302)+(14.001), (I-302)+(14.002), (I-302)+(15.008), (I-302)+(15.012), (I-302)+(15.016), (I-302)+(15.027), (I-302)+(15.043), (I-302)+(15.047), (I-302)+(15.048), (I-302)+(15.052), (I-302)+(15.062), (I-302)+(15.064), (I-302)+(16.001), (I-302)+(17.001), (I-302)+(17.012) and (I-302)+(18.001).

Even more preferred compound combinations are also selected from the group (G4-A) consisting of the following mixtures:

(I-302)+(1.002), (I-302)+(1.004), (I-302)+(1.010), (I-302)+(1.012), (I-302)+(1.018), (I-302)+(1.020), (I-302)+(1.021), (I-302)+(1.026), (I-302)+(1.027), (I-302)+(1.055), (I-302)+(1.059), (I-302)+(1.081), (I-302)+(1.082), (I-302)+(1.092), (I-302)+(2.001), (I-302)+(2.002), (I-302)+(2.003), (I-302)+(2.005), (I-302)+(2.007), (I-302)+(2.017), (I-302)+(2.018), (I-302)+(2.019), (I-302)+(2.021), (I-302)+(2.028), (I-302)+(2.030), (I-302)+(2.038), (I-302)+(3.003), (I-302)+(3.012), (I-302)+(3.016), (I-302)+(3.017), (I-302)+(3.020), (I-302)+(3.025), (I-302)+(3.026), (I-302)+(3.030), (I-302)+(3.031), (I-302)+(4.005), (I-302)+(4.007), (I-302)+(4.012), (I-302)+(4.015), (I-302)+(4.025), (I-302)+(5.003), (I-302)+(5.004), (I-302)+(5.010), (I-302)+(5.012), (I-302)+(5.013), (I-302)+(5.015), (I-302)+(5.018), (I-302)+(6.002), (I-302)+(7.005), (I-302)+(9.004), (I-302)+(12.003), (I-302)+(12.004), (I-302)+(13.001), (I-302)+(13.004), (I-302)+(13.005), (I-302)+(14.001), (I-302)+(14.002), (I-302)+(15.008), (I-302)+(15.012), (I-302)+(15.016), (I-302)+(15.027), (I-302)+(15.047), (I-302)+(15.048), (I-302)+(15.052), (I-302)+(15.062), (I-302)+(15.064), (I-302)+(16.001), (I-302)+(17.001), (I-302)+(17.012) and (I-302)+(18.001).

Even more preferred compound combinations are also selected from the group (G6-1A) consisting of the following mixtures:

(I-339)+(1.002), (I-339)+(1.004), (I-339)+(1.010), (I-339)+(1.012), (I-339)+(1.018), (I-339)+(1.020), (I-339)+(1.021), (I-339)+(1.026), (I-339)+(1.027), (I-339)+(1.055), (I-339)+(1.059), (I-339)+(1.062), (I-339)+(1.067), (I-339)+(1.081), (I-339)+(1.082), (I-339)+(1.092), (I-339)+(2.001), (I-339)+(2.002), (I-339)+(2.003), (I-339)+(2.005), (I-339)+(2.007), (I-339)+(2.017), (I-339)+(2.018), (I-339)+(2.019), (I-339)+(2.021), (I-339)+(2.028), (I-339)+(2.030), (I-339)+(2.038), (I-339)+(3.003), (I-339)+(3.012), (I-339)+(3.016), (I-339)+(3.017), (I-339)+(3.020), (I-339)+(3.025), (I-339)+(3.026), (I-339)+(3.030), (I-339)+(3.031), (I-339)+(4.005), (I-339)+(4.007), (I-339)+(4.012), (I-339)+(4.015), (I-339)+(4.025), (I-339)+(5.003), (I-339)+(5.004), (I-339)+(5.010), (I-339)+(5.012), (I-339)+(5.013), (I-339)+(5.015), (I-339)+(5.018), (I-339)+(6.002), (I-339)+(7.005), (I-339)+(9.004), (I-339)+(12.003), (I-339)+(12.004), (I-339)+(13.001), (I-339)+(13.004), (I-339)+(13.005), (I-339)+(14.001), (I-339)+(14.002), (I-339)+(15.008), (I-339)+(15.012), (I-339)+(15.016), (I-339)+(15.027), (I-339)+(15.043), (I-339)+(15.047), (I-339)+(15.048), (I-339)+(15.052), (I-339)+(15.062), (I-339)+(15.064), (I-339)+(16.001), (I-339)+(17.001), (I-339)+(17.012) and (I-339)+(18.001).

Even more preferred compound combinations are also selected from the group (G7-1A) consisting of the following mixtures:

(I-338)+(1.002), (I-338)+(1.004), (I-338)+(1.010), (I-338)+(1.012), (I-338)+(1.018), (I-338)+(1.020), (I-338)+(1.021), (I-338)+(1.026), (I-338)+(1.027), (I-338)+(1.055), (I-338)+(1.059), (I-338)+(1.062), (I-338)+(1.067), (I-338)+(1.081), (I-338)+(1.082), (I-338)+(1.092), (I-338)+(2.001), (I-338)+(2.002), (I-338)+(2.003), (I-338)+(2.005), (I-338)+(2.007), (I-338)+(2.017), (I-338)+(2.018), (I-338)+(2.019), (I-338)+(2.021), (I-338)+(2.028), (I-338)+(2.030), (I-338)+(2.038), (I-338)+(3.003), (I-338)+(3.012), (I-338)+(3.016), (I-338)+(3.017), (I-338)+(3.020), (I-338)+(3.025), (I-338)+(3.026), (I-338)+(3.030), (I-338)+(3.031), (I-338)+(4.005), (I-338)+(4.007), (I-338)+(4.012), (I-338)+(4.015), (I-338)+(4.025), (I-338)+(5.003), (I-338)+(5.004), (I-338)+(5.010), (I-338)+(5.012), (I-338)+(5.013), (I-338)+(5.015), (I-338)+(5.018), (I-338)+(6.002), (I-338)+(7.005), (I-338)+(9.004), (I-338)+(12.003), (I-338)+(12.004), (I-338)+(13.001), (I-338)+(13.004), (I-338)+(13.005), (I-338)+(14.001), (I-338)+(14.002), (I-338)+(15.008), (I-338)+(15.012), (I-338)+(15.016), (I-338)+(15.027), (I-338)+(15.043), (I-338)+(15.047), (I-338)+(15.048), (I-338)+(15.052), (I-338)+(15.062), (I-338)+(15.064), (I-338)+(16.001), (I-338)+(17.001), (I-338)+(17.012) and (I-338)+(18.001).

Still even more preferred compound combinations are selected from the group (G1-A) consisting of the following mixtures:

(I-052)+(1.002), (I-052)+(1.018), (I-052)+(1.020), (I-052)+(1.021), (I-052)+(1.055), (I-052)+(2.002), (I-052)+(2.005), (I-052)+(2.028), (I-052)+(2.038), (I-052)+(3.020), (I-052)+(3.025), (I-052)+(5.003), (I-052)+(5.010), (I-052)+(5.012), (I-052)+(5.013), (I-052)+(5.018), (I-052)+(6.002), (I-052)+(7.005), (I-052)+(13.001), (I-052)+(13.004), (I-052)+(13.005), (I-052)+(15.012), (I-052)+(15.016), (I-052)+(15.064), (I-052)+(17.001), (I-052)+(17.012) and (I-052)+(18.001).

Still even more preferred compound combinations are also selected from the group (G3-A) consisting of the following mixtures:

(I-300)+(1.002), (I-300)+(1.018), (I-300)+(1.020), (I-300)+(1.021), (I-300)+(1.055), (I-300)+(2.002), (I-300)+(2.005), (I-300)+(2.028), (I-300)+(2.038), (I-300)+(3.020), (I-300)+(3.025), (I-300)+(5.003), (I-300)+(5.010), (I-300)+(5.012), (I-300)+(5.013), (I-300)+(5.018), (I-300)+(6.002), (I-300)+(7.005), (I-300)+(13.001), (I-300)+(13.004), (I-300)+(13.005), (I-300)+(15.012), (I-300)+(15.016), (I-300)+(15.064), (I-300)+(17.001), (I-300)+(17.012) and (I-300)+(18.001).

Still even more preferred compound combinations are also selected from the group (G4-A) consisting of the following mixtures:

(I-302)+(1.002), (I-302)+(1.018), (I-302)+(1.020), (I-302)+(1.021), (I-302)+(1.055), (I-302)+(2.002), (I-302)+(2.005), (I-302)+(2.028), (I-302)+(2.038), (I-302)+(3.020), (I-302)+(3.025), (I-302)+(5.003), (I-302)+(5.010), (I-302)+(5.012), (I-302)+(5.013), (I-302)+(5.018), (I-302)+(6.002), (I-302)+(7.005), (I-302)+(13.001), (I-302)+(13.004), (I-302)+(13.005), (I-302)+(15.012), (I-302)+(15.016), (I-302)+(15.064), (I-300)+(17.001), (I-302)+(17.012) and (I-302)+(18.001).

Still even more preferred compound combinations are also selected from the group (G2-1A) consisting of the following mixtures:

(I-130)+(1.002), (I-130)+(1.018), (I-130)+(1.020), (I-130)+(1.021), (I-130)+(1.055), (I-130)+(1.067), (I-130)+(2.002), (I-130)+(2.005), (I-130)+(2.017), (I-130)+(2.028), (I-130)+(2.038), (I-130)+(3.012), (I-130)+(3.025), (I-130)+(3.030), (I-130)+(5.003), (I-130)+(5.010), (I-130)+(5.012), (I-130)+(5.013), (I-130)+(5.018), (I-130)+(6.002), (I-130)+(7.005), (I-130)+(12.004), (I-130)+(13.001), (I-130)+(13.004), (I-130)+(13.005), (I-130)+(15.012), (I-130)+(15.016), (I-130)+(15.043), (I-130)+(17.001) and (I-130)+(17.012)

Still even more preferred compound combinations are also selected from the group (G7-A1) consisting of the following mixtures:

(I-338)+(1.002), (I-338)+(1.018), (I-338)+(1.020), (I-338)+(1.021), (I-338)+(1.055), (I-338)+(1.067), (I-338)+(2.002), (I-338)+(2.005), (I-338)+(2.017), (I-338)+(2.028), (I-338)+(2.038), (I-338)+(3.012), (I-338)+(3.020), (I-338)+(3.025), (I-338)+(3.030), (I-338)+(5.003), (I-338)+(5.010), (I-338)+(5.012), (I-338)+(5.013), (I-338)+(5.018), (I-338)+(6.002), (I-338)+(7.005), (I-338)+(12.004), (I-338)+(13.001), (I-338)+(13.004), (I-338)+(13.005), (I-338)+(15.012), (I-338)+(15.016), (I-338)+(15.043), (I-338)+(17.001) and (I-338)+(17.012)

Still even more preferred compound combinations are also selected from the group (G6-A1) consisting of the following mixtures:

(I-339)+(1.002), (I-339)+(1.018), (I-339)+(1.020), (I-339)+(1.021), (I-339)+(1.055), (I-339)+(1.067), (I-339)+(2.002), (I-339)+(2.005), (I-339)+(2.017), (I-339)+(2.028), (I-339)+(2.038), (I-339)+(3.012), (I-339)+(3.020), (I-339)+(3.025), (I-339)+(3.030), (I-339)+(5.003), (I-339)+(5.010), (I-339)+(5.012), (I-339)+(5.013), (I-339)+(5.018), (I-339)+(6.002), (I-339)+(7.005), (I-339)+(12.004), (I-339)+(13.001), (I-339)+(13.004), (I-339)+(13.005), (I-339)+(15.012), (I-339)+(15.016), (I-339)+(15.043), (I-339)+(17.001) and (I-339)+(17.012)

If two compounds (B) are present in the combinations according to the invention, preferred compound combinations are selected from the group (G1-C) consisting of the following mixtures:

(I-052)+(1.001)+(1.002), (I-052)+(1.001)+(1.003), (I-052)+(1.001)+(1.004), (I-052)+(1.001)+(1.005), (I-052)+(1.001)+(1.006), (I-052)+(1.001)+(1.007), (I-052)+(1.001)+(1.008), (I-052)+(1.001)+(1.009), (I-052)+(1.001)+(1.010), (I-052)+(1.001)+(1.011), (I-052)+(1.001)+(1.012), (I-052)+(1.001)+(1.013), (I-052)+(1.001)+(1.014), (I-052)+(1.001)+(1.015), (I-052)+(1.001)+(1.016), (I-052)+(1.001)+(1.017), (I-052)+(1.001)+(1.018), (I-052)+(1.001)+(1.019), (I-052)+(1.001)+(1.020), (I-052)+(1.001)+(1.021), (I-052)+(1.001)+(1.022), (I-052)+(1.001)+(1.023), (I-052)+(1.001)+(1.024), (I-052)+(1.001)+(1.025), (I-052)+(1.001)+(1.026), (I-052)+(1.001)+(1.027), (I-052)+(1.001)+(1.028), (I-052)+(1.001)+(1.029), (I-052)+(1.001)+(1.030), (I-052)+(1.001)+(1.031), (I-052)+(1.001)+(1.032), (I-052)+(1.001)+(1.033), (I-052)+(1.001)+(1.034), (I-052)+(1.001)+(1.035), (I-052)+(1.001)+(1.036), (I-052)+(1.001)+(1.037), (I-052)+(1.001)+(1.038), (I-052)+(1.001)+(1.039), (I-052)+(1.001)+(1.040), (I-052)+(1.001)+(1.041), (I-052)+(1.001)+(1.042), (I-052)+(1.001)+(1.043), (I-052)+(1.001)+(1.044), (I-052)+(1.001)+(1.045), (I-052)+(1.001)+(1.046), (I-052)+(1.001)+(1.047), (I-052)+(1.001)+(1.048), (I-052)+(1.001)+(1.049), (I-052)+(1.001)+(1.050), (I-052)+(1.001)+(1.051), (I-052)+(1.001)+(1.052), (I-052)+(1.001)+(1.053), (I-052)+(1.001)+(1.054), (I-052)+(1.001)+(1.055), (I-052)+(1.001)+(1.056), (I-052)+(1.001)+(1.057), (I-052)+(1.001)+(1.058), (I-052)+(1.001)+(1.059), (I-052)+(1.001)+(1.060), (I-052)+(1.001)+(1.061), (I-052)+(1.001)+(1.062), (I-052)+(1.001)+(1.063), (I-052)+(1.001)+(1.064), (I-052)+(1.001)+(1.065), (I-052)+(1.001)+(1.066), (I-052)+(1.001)+(1.067), (I-052)+(1.001)+(1.068), (I-052)+(1.001)+(1.069), (I-052)+(1.001)+(1.070), (I-052)+(1.001)+(1.071), (I-052)+(1.001)+(1.072), (I-052)+(1.001)+(1.073), (I-052)+(1.001)+(1.074), (I-052)+(1.001)+(1.075), (I-052)+(1.001)+(1.076), (I-052)+(1.001)+(1.077), (I-052)+(1.001)+(1.078), (I-052)+(1.001)+(1.079), (I-052)+(1.001)+(1.080), (I-052)+(1.001)+(1.081), (I-052)+(1.001)+(1.082), (I-052)+(1.001)+(1.083), (I-052)+(1.001)+(1.084), (I-052)+(1.001)+(1.085), (I-052)+(1.001)+(1.086), (I-052)+(1.001)+(1.087), (I-052)+(1.001)+(1.088), (I-052)+(1.001)+(1.089), (I-052)+(1.001)+(1.090), (I-052)+(1.001)+(1.091), (I-052)+(1.001)+(1.092), (I-052)+(1.001)+(2.001), (I-052)+(1.001)+(2.002), (I-052)+(1.001)+(2.003), (I-052)+(1.001)+(2.004), (I-052)+(1.001)+(2.005), (I-052)+(1.001)+(2.006), (I-052)+(1.001)+(2.007), (I-052)+(1.001)+(2.008), (I-052)+(1.001)+(2.009), (I-052)+(1.001)+(2.010), (I-052)+(1.001)+(2.011), (I-052)+(1.001)+(2.012), (I-052)+(1.001)+(2.013), (I-052)+(1.001)+(2.014), (I-052)+(1.001)+(2.015), (I-052)+(1.001)+(2.016), (I-052)+(1.001)+(2.017), (I-052)+(1.001)+(2.018), (I-052)+(1.001)+(2.019), (I-052)+(1.001)+(2.020), (I-052)+(1.001)+(2.021), (I-052)+(1.001)+(2.022), (I-052)+(1.001)+(2.023), (I-052)+(1.001)+(2.024), (I-052)+(1.001)+(2.025), (I-052)+(1.001)+(2.026), (I-052)+(1.001)+(2.027), (I-052)+(1.001)+(2.028), (I-052)+(1.001)+(2.029), (I-052)+(1.001)+(2.030), (I-052)+(1.001)+(2.031), (I-052)+(1.001)+(2.032), (I-052)+(1.001)+(2.033), (I-052)+(1.001)+(2.034), (I-052)+(1.001)+(2.035), (I-052)+(1.001)+(2.036), (I-052)+(1.001)+(2.037), (I-052)+(1.001)+(2.038), (I-052)+(1.001)+(2.039), (I-052)+(1.001)+(2.040), (I-052)+(1.001)+(2.041), (I-052)+(1.001)+(2.042), (I-052)+(1.001)+(2.043), (I-052)+(1.001)+(2.044), (I-052)+(1.001)+(2.045), (I-052)+(1.001)+(2.046), (I-052)+(1.001)+(2.047), (I-052)+(1.001)+(2.048), (I-052)+(1.001)+(2.049), (I-052)+(1.001)+(2.050), (I-052)+(1.001)+(2.051), (I-052)+(1.001)+(2.052), (I-052)+(1.001)+(2.053), (I-052)+(1.001)+(2.054), (I-052)+(1.001)+(2.055), (I-052)+(1.001)+(2.056), (I-052)+(1.001)+(2.057), (I-052)+(1.001)+(2.058), (I-052)+(1.001)+(2.059), (I-052)+(1.001)+(3.001), (I-052)+(1.001)+(3.002), (I-052)+(1.001)+(3.003), (I-052)+(1.001)+(3.004), (I-052)+(1.001)+(3.005), (I-052)+(1.001)+(3.006), (I-052)+(1.001)+(3.007), (I-052)+(1.001)+(3.008), (I-052)+(1.001)+(3.009), (I-052)+(1.001)+(3.010), (I-052)+(1.001)+(3.011), (I-052)+(1.001)+(3.012), (I-052)+(1.001)+(3.013), (I-052)+(1.001)+(3.014), (I-052)+(1.001)+(3.015), (I-052)+(1.001)+(3.016), (I-052)+(1.001)+(3.017), (I-052)+(1.001)+(3.018), (I-052)+(1.001)+(3.019), (I-052)+(1.001)+(3.020), (I-052)+(1.001)+(3.021), (I-052)+(1.001)+(3.022), (I-052)+(1.001)+(3.023), (I-052)+(1.001)+(3.024), (I-052)+(1.001)+(3.025), (I-052)+(1.001)+(3.026), (I-052)+(1.001)+(3.027), (I-052)+(1.001)+(3.028), (I-052)+(1.001)+(3.029), (I-052)+(1.001)+(3.030), (I-052)+(1.001)+(3.031), (I-052)+(1.001)+(5.001), (I-052)+(1.001)+(5.002), (I-052)+(1.001)+(5.003), (I-052)+(1.001)+(5.004), (I-052)+(1.001)+(5.005), (I-052)+(1.001)+(5.006), (I-052)+(1.001)+(5.007), (I-052)+(1.001)+(5.008), (I-052)+(1.001)+(5.009), (I-052)+(1.001)+(5.010), (I-052)+(1.001)+(5.011), (I-052)+(1.001)+(5.012), (I-052)+(1.001)+(5.013), (I-052)+(1.001)+(5.014), (I-052)+(1.001)+(5.015), (I-052)+(1.001)+(5.016), (I-052)+(1.001)+(5.017), (I-052)+(1.001)+(5.018), (I-052)+(1.001)+(5.019), 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(I-052)+(3.031)+(5.008), (I-052)+(3.031)+(5.009), (I-052)+(3.031)+(5.010), (I-052)+(3.031)+(5.011), (I-052)+(3.031)+(5.012), (I-052)+(3.031)+(5.013), (I-052)+(3.031)+(5.014), (I-052)+(3.031)+(5.015), (I-052)+(3.031)+(5.016), (I-052)+(3.031)+(5.017), (I-052)+(3.031)+(5.018), (I-052)+(3.031)+(5.019), (I-052)+(3.031)+(5.020), (I-052)+(3.031)+(5.021), (I-052)+(3.031)+(5.022), (I-052)+(3.031)+(5.023), (I-052)+(3.031)+(6.001), (I-052)+(3.031)+(6.002), (I-052)+(3.031)+(6.003), (I-052)+(3.031)+(6.004), (I-052)+(3.031)+(7.001), (I-052)+(3.031)+(7.002), (I-052)+(3.031)+(7.003), (I-052)+(3.031)+(7.004), (I-052)+(3.031)+(7.005), (I-052)+(3.031)+(7.006), (I-052)+(3.031)+(9.001), (I-052)+(3.031)+(9.002), (I-052)+(3.031)+(9.003), (I-052)+(3.031)+(9.004), (I-052)+(3.031)+(9.005), (I-052)+(3.031)+(9.006), (I-052)+(3.031)+(9.007), (I-052)+(3.031)+(9.008), (I-052)+(3.031)+(9.009), (I-052)+(3.031)+(14.001), (I-052)+(3.031)+(14.002), (I-052)+(3.031)+(15.008), (I-052)+(3.031)+(15.011), (I-052)+(3.031)+(15.012), (I-052)+(3.031)+(15.016), (I-052)+(3.031)+(15.025), (I-052)+(3.031)+(15.027), (I-052)+(3.031)+(15.047), (I-052)+(3.031)+(15.063), (I-052)+(3.031)+(15.064), (I-052)+(3.031)+(16.001), (I-052)+(3.031)+(16.002), (I-052)+(3.031)+(16.003), (I-052)+(3.031)+(16.004), (I-052)+(3.031)+(16.005), (I-052)+(3.031)+(16.006), (I-052)+(3.031)+(16.007), (I-052)+(3.031)+(16.008), (I-052)+(3.031)+(17.001), (I-052)+(3.031)+(17.002), (I-052)+(3.031)+(17.003), (I-052)+(3.031)+(17.004), (I-052)+(3.031)+(17.005), (I-052)+(3.031)+(17.006), (I-052)+(3.031)+(17.007), (I-052)+(3.031)+(17.008), (I-052)+(3.031)+(17.009), (I-052)+(3.031)+(17.010), (I-052)+(3.031)+(17.011), (I-052)+(3.031)+(17.012), (I-052)+(3.031)+(18.001), (I-052)+(5.001)+(9.001), (I-052)+(5.001)+(9.002), (I-052)+(5.001)+(9.003), (I-052)+(5.001)+(9.004), (I-052)+(5.001)+(9.005), (I-052)+(5.001)+(9.006), (1-052)+(5.001)+(9.007), (I-052)+(5.001)+(9.008), (I-052)+(5.001)+(9.009), (I-052)+(5.001)+(15.012), (I-052)+(5.001)+(15.016), (I-052)+(5.001)+(15.025), (I-052)+(5.001)+(15.027), (I-052)+(5.001)+(15.047), (I-052)+(5.001)+(15.063), (I-052)+(5.001)+(15.064), (I-052)+(5.002)+(9.001), (I-052)+(5.002)+(9.002), (I-052)+(5.002)+(9.003), (I-052)+(5.002)+(9.004), (I-052)+(5.002)+(9.005), (I-052)+(5.002)+(9.006), (I-052)+(5.002)+(9.007), (I-052)+(5.002)+(9.008), (I-052)+(5.002)+(9.009), (I-052)+(5.002)+(15.012), (I-052)+(5.002)+(15.016), (I-052)+(5.002)+(15.025), (I-052)+(5.002)+(15.027), (I-052)+(5.002)+(15.047), (I-052)+(5.002)+(15.063), (I-052)+(5.002)+(15.064), (I-052)+(5.003)+(9.001), (I-052)+(5.003)+(9.002), (I-052)+(5.003)+(9.003), (I-052)+(5.003)+(9.004), (I-052)+(5.003)+(9.005), (I-052)+(5.003)+(9.006), (I-052)+(5.003)+(9.007), (I-052)+(5.003)+(9.008), (I-052)+(5.003)+(9.009), (I-052)+(5.003)+(15.012), (I-052)+(5.003)+(15.016), (I-052)+(5.003)+(15.025), (I-052)+(5.003)+(15.027), (I-052)+(5.003)+(15.047), (I-052)+(5.003)+(15.063), (I-052)+(5.003)+(15.064), (I-052)+(5.004)+(9.001), (I-052)+(5.004)+(9.002), (I-052)+(5.004)+(9.003), (I-052)+(5.004)+(9.004), (I-052)+(5.004)+(9.005), (I-052)+(5.004)+(9.006), (I-052)+(5.004)+(9.007), (I-052)+(5.004)+(9.008), (I-052)+(5.004)+(9.009), (I-052)+(5.004)+(15.012), (I-052)+(5.004)+(15.016), (I-052)+(5.004)+(15.025), (I-052)+(5.004)+(15.027), (I-052)+(5.004)+(15.047), (I-052)+(5.004)+(15.063), (I-052)+(5.004)+(15.064), (I-052)+(5.005)+(9.001), (I-052)+(5.005)+(9.002), (I-052)+(5.005)+(9.003), (I-052)+(5.005)+(9.004), (I-052)+(5.005)+(9.005), (I-052)+(5.005)+(9.006), (I-052)+(5.005)+(9.007), (I-052)+(5.005)+(9.008), (I-052)+(5.005)+(9.009), (I-052)+(5.005)+(15.012), (I-052)+(5.005)+(15.016), (I-052)+(5.005)+(15.025), (I-052)+(5.005)+(15.027), (I-052)+(5.005)+(15.047), (I-052)+(5.005)+(15.063), (I-052)+(5.005)+(15.064), (I-052)+(5.006)+(9.001), (I-052)+(5.006)+(9.002), (I-052)+(5.006)+(9.003), (I-052)+(5.006)+(9.004), (I-052)+(5.006)+(9.005), (I-052)+(5.006)+(9.006), (I-052)+(5.006)+(9.007), (I-052)+(5.006)+(9.008), (I-052)+(5.006)+(9.009), (I-052)+(5.006)+(15.012), (I-052)+(5.006)+(15.016), (I-052)+(5.006)+(15.025), (I-052)+(5.006)+(15.027), (I-052)+(5.006)+(15.047), (I-052)+(5.006)+(15.063), (I-052)+(5.006)+(15.064), (I-052)+(5.007)+(9.001), (I-052)+(5.007)+(9.002), (I-052)+(5.007)+(9.003), (I-052)+(5.007)+(9.004), (I-052)+(5.007)+(9.005), (I-052)+(5.007)+(9.006), (I-052)+(5.007)+(9.007), (I-052)+(5.007)+(9.008), (I-052)+(5.007)+(9.009), (I-052)+(5.007)+(15.012), (I-052)+(5.007)+(15.016), (I-052)+(5.007)+(15.025), (I-052)+(5.007)+(15.027), (I-052)+(5.007)+(15.047), (I-052)+(5.007)+(15.063), (I-052)+(5.007)+(15.064), (I-052)+(5.008)+(9.001), (I-052)+(5.008)+(9.002), (I-052)+(5.008)+(9.003), (I-052)+(5.008)+(9.004), (I-052)+(5.008)+(9.005), (I-052)+(5.008)+(9.006), (I-052)+(5.008)+(9.007), (I-052)+(5.008)+(9.008), (I-052)+(5.008)+(9.009), (I-052)+(5.008)+(15.012), (I-052)+(5.008)+(15.016), (I-052)+(5.008)+(15.025), (I-052)+(5.008)+(15.027), (I-052)+(5.008)+(15.047), (I-052)+(5.008)+(15.063), (I-052)+(5.008)+(15.064), (I-052)+(5.009)+(9.001), (I-052)+(5.009)+(9.002), (I-052)+(5.009)+(9.003), (I-052)+(5.009)+(9.004), (I-052)+(5.009)+(9.005), (I-052)+(5.009)+(9.006), (I-052)+(5.009)+(9.007), (I-052)+(5.009)+(9.008), (I-052)+(5.009)+(9.009), (I-052)+(5.009)+(15.012), (I-052)+(5.009)+(15.016), (I-052)+(5.009)+(15.025), (I-052)+(5.009)+(15.027), (I-052)+(5.009)+(15.047), (I-052)+(5.009)+(15.063), (I-052)+(5.009)+(15.064), (I-052)+(5.010)+(9.001), (I-052)+(5.010)+(9.002), (I-052)+(5.010)+(9.003), (I-052)+(5.010)+(9.004), (I-052)+(5.010)+(9.005), (I-052)+(5.010)+(9.006), (I-052)+(5.010)+(9.007), (I-052)+(5.010)+(9.008), (I-052)+(5.010)+(9.009), (I-052)+(5.010)+(15.012), (I-052)+(5.010)+(15.016), (I-052)+(5.010)+(15.025), (I-052)+(5.010)+(15.027), (I-052)+(5.010)+(15.047), (I-052)+(5.010)+(15.063), (I-052)+(5.010)+(15.064), (I-052)+(5.011)+(9.001), (I-052)+(5.011)+(9.002), (I-052)+(5.011)+(9.003), (I-052)+(5.011)+(9.004), (I-052)+(5.011)+(9.005), (I-052)+(5.011)+(9.006), (I-052)+(5.011)+(9.007), (I-052)+(5.011)+(9.008), (I-052)+(5.011)+(9.009), (I-052)+(5.011)+(15.012), (I-052)+(5.011)+(15.016), (I-052)+(5.011)+(15.025), (I-052)+(5.011)+(15.027), (I-052)+(5.011)+(15.047), (I-052)+(5.011)+(15.063), (I-052)+(5.011)+(15.064), (I-052)+(5.012)+(9.001), (I-052)+(5.012)+(9.002), (I-052)+(5.012)+(9.003), (I-052)+(5.012)+(9.004), (I-052)+(5.012)+(9.005), (I-052)+(5.012)+(9.006), (I-052)+(5.012)+(9.007), (I-052)+(5.012)+(9.008), (I-052)+(5.012)+(9.009), (I-052)+(5.012)+(15.012), (I-052)+(5.012)+(15.016), (I-052)+(5.012)+(15.025), (I-052)+(5.012)+(15.027), (I-052)+(5.012)+(15.047), (I-052)+(5.012)+(15.063), (I-052)+(5.012)+(15.064), (I-052)+(5.013)+(9.001), (I-052)+(5.013)+(9.002), (I-052)+(5.013)+(9.003), (I-052)+(5.013)+(9.004), (I-052)+(5.013)+(9.005), (I-052)+(5.013)+(9.006), (I-052)+(5.013)+(9.007), (I-052)+(5.013)+(9.008), (I-052)+(5.013)+(9.009), (I-052)+(5.013)+(15.012), (I-052)+(5.013)+(15.016), (I-052)+(5.013)+(15.025), (I-052)+(5.013)+(15.027), (I-052)+(5.013)+(15.047), (I-052)+(5.013)+(15.063), (I-052)+(5.013)+(15.064), (I-052)+(5.014)+(9.001), (I-052)+(5.014)+(9.002), (I-052)+(5.014)+(9.003), (I-052)+(5.014)+(9.004), (I-052)+(5.014)+(9.005), (I-052)+(5.014)+(9.006), (I-052)+(5.014)+(9.007), (I-052)+(5.014)+(9.008), (I-052)+(5.014)+(9.009), (I-052)+(5.014)+(15.012), (I-052)+(5.014)+(15.016), (I-052)+(5.014)+(15.025), (I-052)+(5.014)+(15.027), (I-052)+(5.014)+(15.047), (I-052)+(5.014)+(15.063), (I-052)+(5.014)+(15.064), (I-052)+(5.015)+(9.001), (I-052)+(5.015)+(9.002), (I-052)+(5.015)+(9.003), (I-052)+(5.015)+(9.004), (I-052)+(5.015)+(9.005), (I-052)+(5.015)+(9.006), (I-052)+(5.015)+(9.007), (I-052)+(5.015)+(9.008), (I-052)+(5.015)+(9.009), (I-052)+(5.015)+(15.012), (I-052)+(5.015)+(15.016), (I-052)+(5.015)+(15.025), (I-052)+(5.015)+(15.027), (I-052)+(5.015)+(15.047), (I-052)+(5.015)+(15.063), (I-052)+(5.015)+(15.064), (I-052)+(5.016)+(9.001), (I-052)+(5.016)+(9.002), (I-052)+(5.016)+(9.003), (I-052)+(5.016)+(9.004), (I-052)+(5.016)+(9.005), (I-052)+(5.016)+(9.006), (I-052)+(5.016)+(9.007), (I-052)+(5.016)+(9.008), (I-052)+(5.016)+(9.009), (I-052)+(5.016)+(15.012), (I-052)+(5.016)+(15.016), (I-052)+(5.016)+(15.025), (I-052)+(5.016)+(15.027), (I-052)+(5.016)+(15.047), (I-052)+(5.016)+(15.063), (I-052)+(5.016)+(15.064), (I-052)+(5.017)+(9.001), (I-052)+(5.017)+(9.002), (I-052)+(5.017)+(9.003), (I-052)+(5.017)+(9.004), (I-052)+(5.017)+(9.005), (I-052)+(5.017)+(9.006), (I-052)+(5.017)+(9.007), (I-052)+(5.017)+(9.008), (I-052)+(5.017)+(9.009), (I-052)+(5.017)+(15.012), (I-052)+(5.017)+(15.016), (I-052)+(5.017)+(15.025), (I-052)+(5.017)+(15.027), (I-052)+(5.017)+(15.047), (I-052)+(5.017)+(15.063), (I-052)+(5.017)+(15.064), (I-052)+(5.018)+(9.001), (I-052)+(5.018)+(9.002), (I-052)+(5.018)+(9.003), (I-052)+(5.018)+(9.004), (I-052)+(5.018)+(9.005), (I-052)+(5.018)+(9.006), (I-052)+(5.018)+(9.007), (I-052)+(5.018)+(9.008), (I-052)+(5.018)+(9.009), (I-052)+(5.018)+(15.012), (I-052)+(5.018)+(15.016), (I-052)+(5.018)+(15.025), (I-052)+(5.018)+(15.027), (I-052)+(5.018)+(15.047), (I-052)+(5.018)+(15.063), (I-052)+(5.018)+(15.064), (I-052)+(5.019)+(9.001), (I-052)+(5.019)+(9.002), (I-052)+(5.019)+(9.003), (I-052)+(5.019)+(9.004), (I-052)+(5.019)+(9.005), (I-052)+(5.019)+(9.006), (I-052)+(5.019)+(9.007), (I-052)+(5.019)+(9.008), (I-052)+(5.019)+(9.009), (I-052)+(5.019)+(15.012), (I-052)+(5.019)+(15.016), (I-052)+(5.019)+(15.025), (I-052)+(5.019)+(15.027), (I-052)+(5.019)+(15.047), (I-052)+(5.019)+(15.063), (I-052)+(5.019)+(15.064), (I-052)+(5.020)+(9.001), (I-052)+(5.020)+(9.002), (I-052)+(5.020)+(9.003), (I-052)+(5.020)+(9.004), (I-052)+(5.020)+(9.005), (I-052)+(5.020)+(9.006), (I-052)+(5.020)+(9.007), (I-052)+(5.020)+(9.008), (I-052)+(5.020)+(9.009), (I-052)+(5.020)+(15.012), (I-052)+(5.020)+(15.016), (I-052)+(5.020)+(15.025), (I-052)+(5.020)+(15.027), (I-052)+(5.020)+(15.047), (I-052)+(5.020)+(15.063), (I-052)+(5.020)+(15.064), (I-052)+(5.021)+(9.001), (I-052)+(5.021)+(9.002), (I-052)+(5.021)+(9.003), (I-052)+(5.021)+(9.004), (I-052)+(5.021)+(9.005), (I-052)+(5.021)+(9.006), (I-052)+(5.021)+(9.007), (I-052)+(5.021)+(9.008), (I-052)+(5.021)+(9.009), (I-052)+(5.021)+(15.012), (I-052)+(5.021)+(15.016), (I-052)+(5.021)+(15.025), (I-052)+(5.021)+(15.027), (I-052)+(5.021)+(15.047), (I-052)+(5.021)+(15.063), (I-052)+(5.021)+(15.064), (I-052)+(5.022)+(9.001), (I-052)+(5.022)+(9.002), (I-052)+(5.022)+(9.003), (I-052)+(5.022)+(9.004), (I-052)+(5.022)+(9.005), (I-052)+(5.022)+(9.006), (I-052)+(5.022)+(9.007), (I-052)+(5.022)+(9.008), (I-052)+(5.022)+(9.009), (I-052)+(5.022)+(15.012), (I-052)+(5.022)+(15.016), (I-052)+(5.022)+(15.025), (I-052)+(5.022)+(15.027), (I-052)+(5.022)+(15.047), (I-052)+(5.022)+(15.063), (I-052)+(5.022)+(15.064), (I-052)+(5.023)+(9.001), (I-052)+(5.023)+(9.002), (I-052)+(5.023)+(9.003), (I-052)+(5.023)+(9.004), (I-052)+(5.023)+(9.005), (I-052)+(5.023)+(9.006), (I-052)+(5.023)+(9.007), (I-052)+(5.023)+(9.008), (I-052)+(5.023)+(9.009), (I-052)+(5.023)+(15.012), (I-052)+(5.023)+(15.016), (I-052)+(5.023)+(15.025), (I-052)+(5.023)+(15.027), (I-052)+(5.023)+(15.047), (I-052)+(5.023)+(15.063), (I-052)+(5.023)+(15.064).

If two compounds (B) are present in the combinations according to the invention, preferred compound combinations are also selected from the group (G2-C) consisting of the following mixtures:

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(I-130)+(5.016)+(9.005), (I-130)+(5.016)+(9.006), (I-130)+(5.016)+(9.007), (I-130)+(5.016)+(9.008), (I-130)+(5.016)+(9.009), (I-130)+(5.016)+(15.012), (I-130)+(5.016)+(15.016), (I-130)+(5.016)+(15.025), (I-130)+(5.016)+(15.027), (I-130)+(5.016)+(15.047), (I-130)+(5.016)+(15.063), (I-130)+(5.016)+(15.064), (I-130)+(5.017)+(9.001), (I-130)+(5.017)+(9.002), (I-130)+(5.017)+(9.003), (I-130)+(5.017)+(9.004), (I-130)+(5.017)+(9.005), (I-130)+(5.017)+(9.006), (I-130)+(5.017)+(9.007), (I-130)+(5.017)+(9.008), (I-130)+(5.017)+(9.009), (I-130)+(5.017)+(15.012), (I-130)+(5.017)+(15.016), (I-130)+(5.017)+(15.025), (I-130)+(5.017)+(15.027), (I-130)+(5.017)+(15.047), (I-130)+(5.017)+(15.063), (I-130)+(5.017)+(15.064), (I-130)+(5.018)+(9.001), (I-130)+(5.018)+(9.002), (I-130)+(5.018)+(9.003), (I-130)+(5.018)+(9.004), (I-130)+(5.018)+(9.005), (I-130)+(5.018)+(9.006), (I-130)+(5.018)+(9.007), (I-130)+(5.018)+(9.008), (I-130)+(5.018)+(9.009), (I-130)+(5.018)+(15.012), (I-130)+(5.018)+(15.016), (I-130)+(5.018)+(15.025), (I-130)+(5.018)+(15.027), (I-130)+(5.018)+(15.047), (I-130)+(5.018)+(15.063), (I-130)+(5.018)+(15.064), (I-130)+(5.019)+(9.001), (I-130)+(5.019)+(9.002), (I-130)+(5.019)+(9.003), (I-130)+(5.019)+(9.004), (I-130)+(5.019)+(9.005), (I-130)+(5.019)+(9.006), (I-130)+(5.019)+(9.007), (I-130)+(5.019)+(9.008), (I-130)+(5.019)+(9.009), (I-130)+(5.019)+(15.012), (I-130)+(5.019)+(15.016), (I-130)+(5.019)+(15.025), (I-130)+(5.019)+(15.027), (I-130)+(5.019)+(15.047), (I-130)+(5.019)+(15.063), (I-130)+(5.019)+(15.064), (I-130)+(5.020)+(9.001), (I-130)+(5.020)+(9.002), (I-130)+(5.020)+(9.003), (I-130)+(5.020)+(9.004), (I-130)+(5.020)+(9.005), (I-130)+(5.020)+(9.006), (I-130)+(5.020)+(9.007), (I-130)+(5.020)+(9.008), (I-130)+(5.020)+(9.009), (I-130)+(5.020)+(15.012), (I-130)+(5.020)+(15.016), (I-130)+(5.020)+(15.025), (I-130)+(5.020)+(15.027), (I-130)+(5.020)+(15.047), (I-130)+(5.020)+(15.063), (I-130)+(5.020)+(15.064), (I-130)+(5.021)+(9.001), (I-130)+(5.021)+(9.002), (I-130)+(5.021)+(9.003), (I-130)+(5.021)+(9.004), (I-130)+(5.021)+(9.005), (I-130)+(5.021)+(9.006), (I-130)+(5.021)+(9.007), (I-130)+(5.021)+(9.008), (I-130)+(5.021)+(9.009), (I-130)+(5.021)+(15.012), (I-130)+(5.021)+(15.016), (I-130)+(5.021)+(15.025), (I-130)+(5.021)+(15.027), (I-130)+(5.021)+(15.047), (I-130)+(5.021)+(15.063), (I-130)+(5.021)+(15.064), (I-130)+(5.022)+(9.001), (I-130)+(5.022)+(9.002), (I-130)+(5.022)+(9.003), (I-130)+(5.022)+(9.004), (I-130)+(5.022)+(9.005), (I-130)+(5.022)+(9.006), (I-130)+(5.022)+(9.007), (I-130)+(5.022)+(9.008), (I-130)+(5.022)+(9.009), (I-130)+(5.022)+(15.012), (I-130)+(5.022)+(15.016), (I-130)+(5.022)+(15.025), (I-130)+(5.022)+(15.027), (I-130)+(5.022)+(15.047), (I-130)+(5.022)+(15.063), (I-130)+(5.022)+(15.064), (I-130)+(5.023)+(9.001), (I-130)+(5.023)+(9.002), (I-130)+(5.023)+(9.003), (I-130)+(5.023)+(9.004), (I-130)+(5.023)+(9.005), (I-130)+(5.023)+(9.006), (I-130)+(5.023)+(9.007), (I-130)+(5.023)+(9.008), (I-130)+(5.023)+(9.009), (I-130)+(5.023)+(15.012), (I-130)+(5.023)+(15.016), (I-130)+(5.023)+(15.025), (I-130)+(5.023)+(15.027), (I-130)+(5.023)+(15.047), (I-130)+(5.023)+(15.063), (I-130)+(5.023)+(15.064).

If two compounds (B) are present in the combinations according to the invention, preferred compound combinations are also selected from the group (G3-C) consisting of the following mixtures:

(I-300)+(1.001)+(1.002), (I-300)+(1.001)+(1.003), (I-300)+(1.001)+(1.004), (I-300)+(1.001)+(1.005), (I-300)+(1.001)+(1.006), (I-300)+(1.001)+(1.007), (I-300)+(1.001)+(1.008), (I-300)+(1.001)+(1.009), (I-300)+(1.001)+(1.010), (I-300)+(1.001)+(1.011), (I-300)+(1.001)+(1.012), (I-300)+(1.001)+(1.013), (I-300)+(1.001)+(1.014), (I-300)+(1.001)+(1.015), (I-300)+(1.001)+(1.016), (I-300)+(1.001)+(1.017), (I-300)+(1.001)+(1.018), (I-300)+(1.001)+(1.019), (I-300)+(1.001)+(1.020), (I-300)+(1.001)+(1.021), (I-300)+(1.001)+(1.022), (I-300)+(1.001)+(1.023), (I-300)+(1.001)+(1.024), (I-300)+(1.001)+(1.025), (I-300)+(1.001)+(1.026), (I-300)+(1.001)+(1.027), (I-300)+(1.001)+(1.028), (I-300)+(1.001)+(1.029), (I-300)+(1.001)+(1.030), (I-300)+(1.001)+(1.031), (I-300)+(1.001)+(1.032), (I-300)+(1.001)+(1.033), (I-300)+(1.001)+(1.034), (I-300)+(1.001)+(1.035), (I-300)+(1.001)+(1.036), (I-300)+(1.001)+(1.037), (I-300)+(1.001)+(1.038), (I-300)+(1.001)+(1.039), (I-300)+(1.001)+(1.040), (I-300)+(1.001)+(1.041), (I-300)+(1.001)+(1.042), (I-300)+(1.001)+(1.043), (I-300)+(1.001)+(1.044), (I-300)+(1.001)+(1.045), (I-300)+(1.001)+(1.046), (I-300)+(1.001)+(1.047), (I-300)+(1.001)+(1.048), (I-300)+(1.001)+(1.049), (I-300)+(1.001)+(1.050), (I-300)+(1.001)+(1.051), (I-300)+(1.001)+(1.052), (I-300)+(1.001)+(1.053), (I-300)+(1.001)+(1.054), (I-300)+(1.001)+(1.055), (I-300)+(1.001)+(1.056), (I-300)+(1.001)+(1.057), (I-300)+(1.001)+(1.058), (I-300)+(1.001)+(1.059), (I-300)+(1.001)+(1.060), (I-300)+(1.001)+(1.061), (I-300)+(1.001)+(1.062), (I-300)+(1.001)+(1.063), (I-300)+(1.001)+(1.064), (I-300)+(1.001)+(1.065), (I-300)+(1.001)+(1.066), (I-300)+(1.001)+(1.067), (I-300)+(1.001)+(1.068), (I-300)+(1.001)+(1.069), (I-300)+(1.001)+(1.070), (I-300)+(1.001)+(1.071), (I-300)+(1.001)+(1.072), (I-300)+(1.001)+(1.073), (I-300)+(1.001)+(1.074), (I-300)+(1.001)+(1.075), (I-300)+(1.001)+(1.076), (I-300)+(1.001)+(1.077), (I-300)+(1.001)+(1.078), (I-300)+(1.001)+(1.079), (I-300)+(1.001)+(1.080), (I-300)+(1.001)+(1.081), (I-300)+(1.001)+(1.082), (I-300)+(1.001)+(1.083), (I-300)+(1.001)+(1.084), (I-300)+(1.001)+(1.085), (I-300)+(1.001)+(1.086), (I-300)+(1.001)+(1.087), (I-300)+(1.001)+(1.088), (I-300)+(1.001)+(1.089), (I-300)+(1.001)+(1.090), (I-300)+(1.001)+(1.091), (I-300)+(1.001)+(1.092), (I-300)+(1.001)+(2.001), (I-300)+(1.001)+(2.002), (I-300)+(1.001)+(2.003), (I-300)+(1.001)+(2.004), (I-300)+(1.001)+(2.005), (I-300)+(1.001)+(2.006), (I-300)+(1.001)+(2.007), (I-300)+(1.001)+(2.008), (I-300)+(1.001)+(2.009), (I-300)+(1.001)+(2.010), (I-300)+(1.001)+(2.011), (I-300)+(1.001)+(2.012), (I-300)+(1.001)+(2.013), (I-300)+(1.001)+(2.014), (I-300)+(1.001)+(2.015), (I-300)+(1.001)+(2.016), (I-300)+(1.001)+(2.017), (I-300)+(1.001)+(2.018), (I-300)+(1.001)+(2.019), (I-300)+(1.001)+(2.020), (I-300)+(1.001)+(2.021), (I-300)+(1.001)+(2.022), (I-300)+(1.001)+(2.023), (I-300)+(1.001)+(2.024), (I-300)+(1.001)+(2.025), (I-300)+(1.001)+(2.026), (I-300)+(1.001)+(2.027), (I-300)+(1.001)+(2.028), (I-300)+(1.001)+(2.029), (I-300)+(1.001)+(2.030), (I-300)+(1.001)+(2.031), (I-300)+(1.001)+(2.032), (I-300)+(1.001)+(2.033), (I-300)+(1.001)+(2.034), (I-300)+(1.001)+(2.035), (I-300)+(1.001)+(2.036), (I-300)+(1.001)+(2.037), (I-300)+(1.001)+(2.038), (I-300)+(1.001)+(2.039), (I-300)+(1.001)+(2.040), (I-300)+(1.001)+(2.041), (I-300)+(1.001)+(2.042), (I-300)+(1.001)+(2.043), (I-300)+(1.001)+(2.044), (I-300)+(1.001)+(2.045), (I-300)+(1.001)+(2.046), (I-300)+(1.001)+(2.047), (I-300)+(1.001)+(2.048), (I-300)+(1.001)+(2.049), (I-300)+(1.001)+(2.050), (I-300)+(1.001)+(2.051), (I-300)+(1.001)+(2.052), (I-300)+(1.001)+(2.053), (I-300)+(1.001)+(2.054), (I-300)+(1.001)+(2.055), (I-300)+(1.001)+(2.056), (I-300)+(1.001)+(2.057), (I-300)+(1.001)+(2.058), (I-300)+(1.001)+(2.059), (I-300)+(1.001)+(3.001), (I-300)+(1.001)+(3.002), (I-300)+(1.001)+(3.003), (I-300)+(1.001)+(3.004), (I-300)+(1.001)+(3.005), (I-300)+(1.001)+(3.006), (I-300)+(1.001)+(3.007), (I-300)+(1.001)+(3.008), (I-300)+(1.001)+(3.009), (I-300)+(1.001)+(3.010), (I-300)+(1.001)+(3.011), (I-300)+(1.001)+(3.012), (I-300)+(1.001)+(3.013), (I-300)+(1.001)+(3.014), (I-300)+(1.001)+(3.015), (I-300)+(1.001)+(3.016), (I-300)+(1.001)+(3.017), (I-300)+(1.001)+(3.018), (I-300)+(1.001)+(3.019), (I-300)+(1.001)+(3.020), (I-300)+(1.001)+(3.021), (I-300)+(1.001)+(3.022), (I-300)+(1.001)+(3.023), (I-300)+(1.001)+(3.024), (I-300)+(1.001)+(3.025), (I-300)+(1.001)+(3.026), (I-300)+(1.001)+(3.027), (I-300)+(1.001)+(3.028), (I-300)+(1.001)+(3.029), (I-300)+(1.001)+(3.030), (I-300)+(1.001)+(3.031), (I-300)+(1.001)+(5.001), (I-300)+(1.001)+(5.002), (I-300)+(1.001)+(5.003), (I-300)+(1.001)+(5.004), (I-300)+(1.001)+(5.005), (I-300)+(1.001)+(5.006), (I-300)+(1.001)+(5.007), (I-300)+(1.001)+(5.008), (I-300)+(1.001)+(5.009), (I-300)+(1.001)+(5.010), (I-300)+(1.001)+(5.011), (I-300)+(1.001)+(5.012), (I-300)+(1.001)+(5.013), (I-300)+(1.001)+(5.014), (I-300)+(1.001)+(5.015), (I-300)+(1.001)+(5.016), (I-300)+(1.001)+(5.017), (I-300)+(1.001)+(5.018), (I-300)+(1.001)+(5.019), (I-300)+(1.001)+(5.020), (I-300)+(1.001)+(5.021), (I-300)+(1.001)+(5.022), (I-300)+(1.001)+(5.023), (I-300)+(1.001)+(6.001), (I-300)+(1.001)+(6.002), (I-300)+(1.001)+(6.003), (I-300)+(1.001)+(6.004), (I-300)+(1.001)+(7.001), (I-300)+(1.001)+(7.002), (I-300)+(1.001)+(7.003), (I-300)+(1.001)+(7.004), (I-300)+(1.001)+(7.005), (I-300)+(1.001)+(7.006), (I-300)+(1.001)+(9.001), (I-300)+(1.001)+(9.002), (I-300)+(1.001)+(9.003), (I-300)+(1.001)+(9.004), (I-300)+(1.001)+(9.005), (I-300)+(1.001)+(9.006), (I-300)+(1.001)+(9.007), (I-300)+(1.001)+(9.008), (I-300)+(1.001)+(9.009), (I-300)+(1.001)+(14.001), (I-300)+(1.001)+(14.002), (I-300)+(1.001)+(15.008), (I-300)+(1.001)+(15.011), (I-300)+(1.001)+(15.012), (I-300)+(1.001)+(15.016), (I-300)+(1.001)+(15.025), (I-300)+(1.001)+(15.027), (I-300)+(1.001)+(15.047), (I-300)+(1.001)+(15.063), (I-300)+(1.001)+(15.064), (I-300)+(1.001)+(16.001), (I-300)+(1.001)+(16.002), (I-300)+(1.001)+(16.003), (I-300)+(1.001)+(16.004), (I-300)+(1.001)+(16.005), (I-300)+(1.001)+(16.006), (I-300)+(1.001)+(16.007), (I-300)+(1.001)+(16.008), (I-300)+(1.001)+(17.001), (I-300)+(1.001)+(17.002), (I-300)+(1.001)+(17.003), (I-300)+(1.001)+(17.004), (I-300)+(1.001)+(17.005), (I-300)+(1.001)+(17.006), (I-300)+(1.001)+(17.007), (I-300)+(1.001)+(17.008), (I-300)+(1.001)+(17.009), (I-300)+(1.001)+(17.010), (I-300)+(1.001)+(17.011), (I-300)+(1.001)+(17.012), (I-300)+(1.001)+(18.001), (I-300)+(1.002)+(1.003), (I-300)+(1.002)+(1.004), (I-300)+(1.002)+(1.005), (I-300)+(1.002)+(1.006), (I-300)+(1.002)+(1.007), (I-300)+(1.002)+(1.008), (I-300)+(1.002)+(1.009), (I-300)+(1.002)+(1.010), (I-300)+(1.002)+(1.011), (I-300)+(1.002)+(1.012), (I-300)+(1.002)+(1.013), (I-300)+(1.002)+(1.014), (I-300)+(1.002)+(1.015), (I-300)+(1.002)+(1.016), (I-300)+(1.002)+(1.017), (I-300)+(1.002)+(1.018), (I-300)+(1.002)+(1.019), (I-300)+(1.002)+(1.020), (I-300)+(1.002)+(1.021), (I-300)+(1.002)+(1.022), (I-300)+(1.002)+(1.023), (I-300)+(1.002)+(1.024), (I-300)+(1.002)+(1.025), (I-300)+(1.002)+(1.026), (I-300)+(1.002)+(1.027), (I-300)+(1.002)+(1.028), (I-300)+(1.002)+(1.029), (I-300)+(1.002)+(1.030), (I-300)+(1.002)+(1.031), (I-300)+(1.002)+(1.032), (I-300)+(1.002)+(1.033), (I-300)+(1.002)+(1.034), (I-300)+(1.002)+(1.035), (I-300)+(1.002)+(1.036), (I-300)+(1.002)+(1.037), (I-300)+(1.002)+(1.038), (I-300)+(1.002)+(1.039), (I-300)+(1.002)+(1.040), (I-300)+(1.002)+(1.041), (I-300)+(1.002)+(1.042), (I-300)+(1.002)+(1.043), (I-300)+(1.002)+(1.044), (I-300)+(1.002)+(1.045), (I-300)+(1.002)+(1.046), (I-300)+(1.002)+(1.047), (I-300)+(1.002)+(1.048), (I-300)+(1.002)+(1.049), (I-300)+(1.002)+(1.050), (I-300)+(1.002)+(1.051), (I-300)+(1.002)+(1.052), (I-300)+(1.002)+(1.053), (I-300)+(1.002)+(1.054), (I-300)+(1.002)+(1.055), (I-300)+(1.002)+(1.056), (I-300)+(1.002)+(1.057), (I-300)+(1.002)+(1.058), (I-300)+(1.002)+(1.059), (I-300)+(1.002)+(1.060), (I-300)+(1.002)+(1.061), (I-300)+(1.002)+(1.062), (I-300)+(1.002)+(1.063), (I-300)+(1.002)+(1.064), (I-300)+(1.002)+(1.065), 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(I-300)+(5.004)+(9.002), (I-300)+(5.004)+(9.003), (I-300)+(5.004)+(9.004), (I-300)+(5.004)+(9.005), (I-300)+(5.004)+(9.006), (I-300)+(5.004)+(9.007), (I-300)+(5.004)+(9.008), (I-300)+(5.004)+(9.009), (I-300)+(5.004)+(15.012), (I-300)+(5.004)+(15.016), (I-300)+(5.004)+(15.025), (I-300)+(5.004)+(15.027), (I-300)+(5.004)+(15.047), (I-300)+(5.004)+(15.063), (I-300)+(5.004)+(15.064), (I-300)+(5.005)+(9.001), (I-300)+(5.005)+(9.002), (I-300)+(5.005)+(9.003), (I-300)+(5.005)+(9.004), (I-300)+(5.005)+(9.005), (I-300)+(5.005)+(9.006), (I-300)+(5.005)+(9.007), (I-300)+(5.005)+(9.008), (I-300)+(5.005)+(9.009), (I-300)+(5.005)+(15.012), (I-300)+(5.005)+(15.016), (I-300)+(5.005)+(15.025), (I-300)+(5.005)+(15.027), (I-300)+(5.005)+(15.047), (I-300)+(5.005)+(15.063), (I-300)+(5.005)+(15.064), (I-300)+(5.006)+(9.001), (I-300)+(5.006)+(9.002), (I-300)+(5.006)+(9.003), (I-300)+(5.006)+(9.004), (I-300)+(5.006)+(9.005), (I-300)+(5.006)+(9.006), (I-300)+(5.006)+(9.007), (I-300)+(5.006)+(9.008), (I-300)+(5.006)+(9.009), (I-300)+(5.006)+(15.012), (I-300)+(5.006)+(15.016), (I-300)+(5.006)+(15.025), (I-300)+(5.006)+(15.027), (I-300)+(5.006)+(15.047), (I-300)+(5.006)+(15.063), (I-300)+(5.006)+(15.064), (I-300)+(5.007)+(9.001), (I-300)+(5.007)+(9.002), (I-300)+(5.007)+(9.003), (I-300)+(5.007)+(9.004), (I-300)+(5.007)+(9.005), (I-300)+(5.007)+(9.006), (I-300)+(5.007)+(9.007), (I-300)+(5.007)+(9.008), (I-300)+(5.007)+(9.009), (I-300)+(5.007)+(15.012), (I-300)+(5.007)+(15.016), (I-300)+(5.007)+(15.025), (I-300)+(5.007)+(15.027), (I-300)+(5.007)+(15.047), (I-300)+(5.007)+(15.063), (I-300)+(5.007)+(15.064), (I-300)+(5.008)+(9.001), (I-300)+(5.008)+(9.002), (I-300)+(5.008)+(9.003), (I-300)+(5.008)+(9.004), (I-300)+(5.008)+(9.005), (I-300)+(5.008)+(9.006), (I-300)+(5.008)+(9.007), (I-300)+(5.008)+(9.008), (I-300)+(5.008)+(9.009), (I-300)+(5.008)+(15.012), (I-300)+(5.008)+(15.016), (I-300)+(5.008)+(15.025), (I-300)+(5.008)+(15.027), (I-300)+(5.008)+(15.047), (I-300)+(5.008)+(15.063), (I-300)+(5.008)+(15.064), (I-300)+(5.009)+(9.001), (I-300)+(5.009)+(9.002), (I-300)+(5.009)+(9.003), (I-300)+(5.009)+(9.004), (I-300)+(5.009)+(9.005), (I-300)+(5.009)+(9.006), (I-300)+(5.009)+(9.007), (I-300)+(5.009)+(9.008), (I-300)+(5.009)+(9.009), (I-300)+(5.009)+(15.012), (I-300)+(5.009)+(15.016), (I-300)+(5.009)+(15.025), (I-300)+(5.009)+(15.027), (I-300)+(5.009)+(15.047), (I-300)+(5.009)+(15.063), (I-300)+(5.009)+(15.064), (I-300)+(5.010)+(9.001), (I-300)+(5.010)+(9.002), (I-300)+(5.010)+(9.003), (I-300)+(5.010)+(9.004), (I-300)+(5.010)+(9.005), (I-300)+(5.010)+(9.006), (I-300)+(5.010)+(9.007), (I-300)+(5.010)+(9.008), (I-300)+(5.010)+(9.009), (I-300)+(5.010)+(15.012), (I-300)+(5.010)+(15.016), (I-300)+(5.010)+(15.025), (I-300)+(5.010)+(15.027), (I-300)+(5.010)+(15.047), (I-300)+(5.010)+(15.063), (I-300)+(5.010)+(15.064), (I-300)+(5.011)+(9.001), (I-300)+(5.011)+(9.002), (I-300)+(5.011)+(9.003), (I-300)+(5.011)+(9.004), (I-300)+(5.011)+(9.005), (I-300)+(5.011)+(9.006), (I-300)+(5.011)+(9.007), (I-300)+(5.011)+(9.008), (I-300)+(5.011)+(9.009), (I-300)+(5.011)+(15.012), (I-300)+(5.011)+(15.016), (I-300)+(5.011)+(15.025), (I-300)+(5.011)+(15.027), (I-300)+(5.011)+(15.047), (I-300)+(5.011)+(15.063), (I-300)+(5.011)+(15.064), (I-300)+(5.012)+(9.001), (I-300)+(5.012)+(9.002), (I-300)+(5.012)+(9.003), (I-300)+(5.012)+(9.004), (I-300)+(5.012)+(9.005), (I-300)+(5.012)+(9.006), (I-300)+(5.012)+(9.007), (I-300)+(5.012)+(9.008), (I-300)+(5.012)+(9.009), (I-300)+(5.012)+(15.012), (I-300)+(5.012)+(15.016), (I-300)+(5.012)+(15.025), (I-300)+(5.012)+(15.027), (I-300)+(5.012)+(15.047), (I-300)+(5.012)+(15.063), (I-300)+(5.012)+(15.064), (I-300)+(5.013)+(9.001), (I-300)+(5.013)+(9.002), (I-300)+(5.013)+(9.003), (I-300)+(5.013)+(9.004), (I-300)+(5.013)+(9.005), (I-300)+(5.013)+(9.006), (I-300)+(5.013)+(9.007), (I-300)+(5.013)+(9.008), (I-300)+(5.013)+(9.009), (I-300)+(5.013)+(15.012), (I-300)+(5.013)+(15.016), (I-300)+(5.013)+(15.025), (I-300)+(5.013)+(15.027), (I-300)+(5.013)+(15.047), (I-300)+(5.013)+(15.063), (I-300)+(5.013)+(15.064), (I-300)+(5.014)+(9.001), (I-300)+(5.014)+(9.002), (I-300)+(5.014)+(9.003), (I-300)+(5.014)+(9.004), (I-300)+(5.014)+(9.005), (I-300)+(5.014)+(9.006), (I-300)+(5.014)+(9.007), (I-300)+(5.014)+(9.008), (I-300)+(5.014)+(9.009), (I-300)+(5.014)+(15.012), (I-300)+(5.014)+(15.016), (I-300)+(5.014)+(15.025), (I-300)+(5.014)+(15.027), (I-300)+(5.014)+(15.047), (I-300)+(5.014)+(15.063), (I-300)+(5.014)+(15.064), (I-300)+(5.015)+(9.001), (I-300)+(5.015)+(9.002), (I-300)+(5.015)+(9.003), (I-300)+(5.015)+(9.004), (I-300)+(5.015)+(9.005), (I-300)+(5.015)+(9.006), (I-300)+(5.015)+(9.007), (I-300)+(5.015)+(9.008), (I-300)+(5.015)+(9.009), (I-300)+(5.015)+(15.012), (I-300)+(5.015)+(15.016), (I-300)+(5.015)+(15.025), (I-300)+(5.015)+(15.027), (I-300)+(5.015)+(15.047), (I-300)+(5.015)+(15.063), (I-300)+(5.015)+(15.064), (I-300)+(5.016)+(9.001), (I-300)+(5.016)+(9.002), (I-300)+(5.016)+(9.003), (I-300)+(5.016)+(9.004), (I-300)+(5.016)+(9.005), (I-300)+(5.016)+(9.006), (I-300)+(5.016)+(9.007), (I-300)+(5.016)+(9.008), (I-300)+(5.016)+(9.009), (I-300)+(5.016)+(15.012), (I-300)+(5.016)+(15.016), (I-300)+(5.016)+(15.025), (I-300)+(5.016)+(15.027), (I-300)+(5.016)+(15.047), (I-300)+(5.016)+(15.063), (I-300)+(5.016)+(15.064), (I-300)+(5.017)+(9.001), (I-300)+(5.017)+(9.002), (I-300)+(5.017)+(9.003), (I-300)+(5.017)+(9.004), (I-300)+(5.017)+(9.005), (I-300)+(5.017)+(9.006), (I-300)+(5.017)+(9.007), (I-300)+(5.017)+(9.008), (I-300)+(5.017)+(9.009), (I-300)+(5.017)+(15.012), (I-300)+(5.017)+(15.016), (I-300)+(5.017)+(15.025), (I-300)+(5.017)+(15.027), (I-300)+(5.017)+(15.047), (I-300)+(5.017)+(15.063), (I-300)+(5.017)+(15.064), (I-300)+(5.018)+(9.001), (I-300)+(5.018)+(9.002), (I-300)+(5.018)+(9.003), (I-300)+(5.018)+(9.004), (I-300)+(5.018)+(9.005), (I-300)+(5.018)+(9.006), (I-300)+(5.018)+(9.007), (I-300)+(5.018)+(9.008), (I-300)+(5.018)+(9.009), (I-300)+(5.018)+(15.012), (I-300)+(5.018)+(15.016), (I-300)+(5.018)+(15.025), (I-300)+(5.018)+(15.027), (I-300)+(5.018)+(15.047), (I-300)+(5.018)+(15.063), (I-300)+(5.018)+(15.064), (I-300)+(5.019)+(9.001), (I-300)+(5.019)+(9.002), (I-300)+(5.019)+(9.003), (I-300)+(5.019)+(9.004), (I-300)+(5.019)+(9.005), (I-300)+(5.019)+(9.006), (I-300)+(5.019)+(9.007), (I-300)+(5.019)+(9.008), (I-300)+(5.019)+(9.009), (I-300)+(5.019)+(15.012), (I-300)+(5.019)+(15.016), (I-300)+(5.019)+(15.025), (I-300)+(5.019)+(15.027), (I-300)+(5.019)+(15.047), (I-300)+(5.019)+(15.063), (I-300)+(5.019)+(15.064), (I-300)+(5.020)+(9.001), (I-300)+(5.020)+(9.002), (I-300)+(5.020)+(9.003), (I-300)+(5.020)+(9.004), (I-300)+(5.020)+(9.005), (I-300)+(5.020)+(9.006), (I-300)+(5.020)+(9.007), (I-300)+(5.020)+(9.008), (I-300)+(5.020)+(9.009), (I-300)+(5.020)+(15.012), (I-300)+(5.020)+(15.016), (I-300)+(5.020)+(15.025), (I-300)+(5.020)+(15.027), (I-300)+(5.020)+(15.047), (I-300)+(5.020)+(15.063), (I-300)+(5.020)+(15.064), (I-300)+(5.021)+(9.001), (I-300)+(5.021)+(9.002), (I-300)+(5.021)+(9.003), (I-300)+(5.021)+(9.004), (I-300)+(5.021)+(9.005), (I-300)+(5.021)+(9.006), (I-300)+(5.021)+(9.007), (I-300)+(5.021)+(9.008), (I-300)+(5.021)+(9.009), (I-300)+(5.021)+(15.012), (I-300)+(5.021)+(15.016), (I-300)+(5.021)+(15.025), (I-300)+(5.021)+(15.027), (I-300)+(5.021)+(15.047), (I-300)+(5.021)+(15.063), (I-300)+(5.021)+(15.064), (I-300)+(5.022)+(9.001), (I-300)+(5.022)+(9.002), (I-300)+(5.022)+(9.003), (I-300)+(5.022)+(9.004), (I-300)+(5.022)+(9.005), (I-300)+(5.022)+(9.006), (I-300)+(5.022)+(9.007), (I-300)+(5.022)+(9.008), (I-300)+(5.022)+(9.009), (I-300)+(5.022)+(15.012), (I-300)+(5.022)+(15.016), (I-300)+(5.022)+(15.025), (I-300)+(5.022)+(15.027), (I-300)+(5.022)+(15.047), (I-300)+(5.022)+(15.063), (I-300)+(5.022)+(15.064), (I-300)+(5.023)+(9.001), (I-300)+(5.023)+(9.002), (I-300)+(5.023)+(9.003), (I-300)+(5.023)+(9.004), (I-300)+(5.023)+(9.005), (I-300)+(5.023)+(9.006), (I-300)+(5.023)+(9.007), (I-300)+(5.023)+(9.008), (I-300)+(5.023)+(9.009), (I-300)+(5.023)+(15.012), (I-300)+(5.023)+(15.016), (I-300)+(5.023)+(15.025), (I-300)+(5.023)+(15.027), (I-300)+(5.023)+(15.047), (I-300)+(5.023)+(15.063), (I-300)+(5.023)+(15.064).

If two compounds (B) are present in the combinations according to the invention, preferred compound combinations are also selected from the group (G4-C) consisting of the following mixtures:

(I-302)+(1.001)+(1.002), (I-302)+(1.001)+(1.003), (I-302)+(1.001)+(1.004), (I-302)+(1.001)+(1.005), (I-302)+(1.001)+(1.006), (I-302)+(1.001)+(1.007), (I-302)+(1.001)+(1.008), (I-302)+(1.001)+(1.009), (I-302)+(1.001)+(1.010), (I-302)+(1.001)+(1.011), (I-302)+(1.001)+(1.012), (I-302)+(1.001)+(1.013), (I-302)+(1.001)+(1.014), (I-302)+(1.001)+(1.015), (I-302)+(1.001)+(1.016), (I-302)+(1.001)+(1.017), (I-302)+(1.001)+(1.018), (I-302)+(1.001)+(1.019), (I-302)+(1.001)+(1.020), (I-302)+(1.001)+(1.021), (I-302)+(1.001)+(1.022), (I-302)+(1.001)+(1.023), (I-302)+(1.001)+(1.024), (I-302)+(1.001)+(1.025), (I-302)+(1.001)+(1.026), (I-302)+(1.001)+(1.027), (I-302)+(1.001)+(1.028), (I-302)+(1.001)+(1.029), (I-302)+(1.001)+(1.030), (I-302)+(1.001)+(1.031), (I-302)+(1.001)+(1.032), (I-302)+(1.001)+(1.033), (I-302)+(1.001)+(1.034), (I-302)+(1.001)+(1.035), (I-302)+(1.001)+(1.036), (I-302)+(1.001)+(1.037), (I-302)+(1.001)+(1.038), (I-302)+(1.001)+(1.039), (I-302)+(1.001)+(1.040), (I-302)+(1.001)+(1.041), (I-302)+(1.001)+(1.042), (I-302)+(1.001)+(1.043), (I-302)+(1.001)+(1.044), (I-302)+(1.001)+(1.045), (I-302)+(1.001)+(1.046), (I-302)+(1.001)+(1.047), (I-302)+(1.001)+(1.048), (I-302)+(1.001)+(1.049), (I-302)+(1.001)+(1.050), (I-302)+(1.001)+(1.051), (I-302)+(1.001)+(1.052), (I-302)+(1.001)+(1.053), (I-302)+(1.001)+(1.054), (I-302)+(1.001)+(1.055), (I-302)+(1.001)+(1.056), (I-302)+(1.001)+(1.057), (I-302)+(1.001)+(1.058), (I-302)+(1.001)+(1.059), (I-302)+(1.001)+(1.060), (I-302)+(1.001)+(1.061), (I-302)+(1.001)+(1.062), (I-302)+(1.001)+(1.063), (I-302)+(1.001)+(1.064), (I-302)+(1.001)+(1.065), (I-302)+(1.001)+(1.066), (I-302)+(1.001)+(1.067), (I-302)+(1.001)+(1.068), (I-302)+(1.001)+(1.069), (I-302)+(1.001)+(1.070), (I-302)+(1.001)+(1.071), (I-302)+(1.001)+(1.072), (I-302)+(1.001)+(1.073), (I-302)+(1.001)+(1.074), (I-302)+(1.001)+(1.075), (I-302)+(1.001)+(1.076), (I-302)+(1.001)+(1.077), (I-302)+(1.001)+(1.078), (I-302)+(1.001)+(1.079), (I-302)+(1.001)+(1.080), (I-302)+(1.001)+(1.081), (I-302)+(1.001)+(1.082), (I-302)+(1.001)+(1.083), (I-302)+(1.001)+(1.084), (I-302)+(1.001)+(1.085), (I-302)+(1.001)+(1.086), (I-302)+(1.001)+(1.087), (I-302)+(1.001)+(1.088), (I-302)+(1.001)+(1.089), (I-302)+(1.001)+(1.090), (I-302)+(1.001)+(1.091), (I-302)+(1.001)+(1.092), (I-302)+(1.001)+(2.001), (I-302)+(1.001)+(2.002), (I-302)+(1.001)+(2.003), (I-302)+(1.001)+(2.004), (I-302)+(1.001)+(2.005), (I-302)+(1.001)+(2.006), (I-302)+(1.001)+(2.007), (I-302)+(1.001)+(2.008), (I-302)+(1.001)+(2.009), (I-302)+(1.001)+(2.010), (I-302)+(1.001)+(2.011), (I-302)+(1.001)+(2.012), (I-302)+(1.001)+(2.013), (I-302)+(1.001)+(2.014), (I-302)+(1.001)+(2.015), (I-302)+(1.001)+(2.016), (I-302)+(1.001)+(2.017), (I-302)+(1.001)+(2.018), (I-302)+(1.001)+(2.019), (I-302)+(1.001)+(2.020), (I-302)+(1.001)+(2.021), (I-302)+(1.001)+(2.022), (I-302)+(1.001)+(2.023), (I-302)+(1.001)+(2.024), (I-302)+(1.001)+(2.025), (I-302)+(1.001)+(2.026), (I-302)+(1.001)+(2.027), (I-302)+(1.001)+(2.028), (I-302)+(1.001)+(2.029), 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(I-302)+(3.030)+(5.007), (I-302)+(3.030)+(5.008), (I-302)+(3.030)+(5.009), (I-302)+(3.030)+(5.010), (I-302)+(3.030)+(5.011), (I-302)+(3.030)+(5.012), (I-302)+(3.030)+(5.013), (I-302)+(3.030)+(5.014), (I-302)+(3.030)+(5.015), (I-302)+(3.030)+(5.016), (I-302)+(3.030)+(5.017), (I-302)+(3.030)+(5.018), (I-302)+(3.030)+(5.019), (I-302)+(3.030)+(5.020), (I-302)+(3.030)+(5.021), (I-302)+(3.030)+(5.022), (I-302)+(3.030)+(5.023), (I-302)+(3.030)+(6.001), (I-302)+(3.030)+(6.002), (I-302)+(3.030)+(6.003), (I-302)+(3.030)+(6.004), (I-302)+(3.030)+(7.001), (I-302)+(3.030)+(7.002), (I-302)+(3.030)+(7.003), (I-302)+(3.030)+(7.004), (I-302)+(3.030)+(7.005), (I-302)+(3.030)+(7.006), (I-302)+(3.030)+(9.001), (I-302)+(3.030)+(9.002), (I-302)+(3.030)+(9.003), (I-302)+(3.030)+(9.004), (I-302)+(3.030)+(9.005), (I-302)+(3.030)+(9.006), (I-302)+(3.030)+(9.007), (I-302)+(3.030)+(9.008), (I-302)+(3.030)+(9.009), (I-302)+(3.030)+(14.001), (I-302)+(3.030)+(14.002), (I-302)+(3.030)+(15.008), (I-302)+(3.030)+(15.011), (I-302)+(3.030)+(15.012), (I-302)+(3.030)+(15.016), (I-302)+(3.030)+(15.025), (I-302)+(3.030)+(15.027), (I-302)+(3.030)+(15.047), (I-302)+(3.030)+(15.063), (I-302)+(3.030)+(15.064), (I-302)+(3.030)+(16.001), (I-302)+(3.030)+(16.002), (I-302)+(3.030)+(16.003), (I-302)+(3.030)+(16.004), (I-302)+(3.030)+(16.005), (I-302)+(3.030)+(16.006), (I-302)+(3.030)+(16.007), (I-302)+(3.030)+(16.008), (I-302)+(3.030)+(17.001), (I-302)+(3.030)+(17.002), (I-302)+(3.030)+(17.003), (I-302)+(3.030)+(17.004), (I-302)+(3.030)+(17.005), (I-302)+(3.030)+(17.006), (I-302)+(3.030)+(17.007), (I-302)+(3.030)+(17.008), (I-302)+(3.030)+(17.009), (I-302)+(3.030)+(17.010), (I-302)+(3.030)+(17.011), (I-302)+(3.030)+(17.012), (I-302)+(3.030)+(18.001), (I-302)+(3.031)+(3.025), (I-302)+(3.031)+(3.030), (I-302)+(3.031)+(5.001), (I-302)+(3.031)+(5.002), (I-302)+(3.031)+(5.003), (I-302)+(3.031)+(5.004), (I-302)+(3.031)+(5.005), (I-302)+(3.031)+(5.006), (I-302)+(3.031)+(5.007), (I-302)+(3.031)+(5.008), (I-302)+(3.031)+(5.009), (I-302)+(3.031)+(5.010), (I-302)+(3.031)+(5.011), (I-302)+(3.031)+(5.012), (I-302)+(3.031)+(5.013), (I-302)+(3.031)+(5.014), (I-302)+(3.031)+(5.015), (I-302)+(3.031)+(5.016), (I-302)+(3.031)+(5.017), (I-302)+(3.031)+(5.018), (I-302)+(3.031)+(5.019), (I-302)+(3.031)+(5.020), (I-302)+(3.031)+(5.021), (I-302)+(3.031)+(5.022), (I-302)+(3.031)+(5.023), (I-302)+(3.031)+(6.001), (I-302)+(3.031)+(6.002), (I-302)+(3.031)+(6.003), (I-302)+(3.031)+(6.004), (I-302)+(3.031)+(7.001), (I-302)+(3.031)+(7.002), (I-302)+(3.031)+(7.003), (I-302)+(3.031)+(7.004), (I-302)+(3.031)+(7.005), (I-302)+(3.031)+(7.006), (I-302)+(3.031)+(9.001), (I-302)+(3.031)+(9.002), (I-302)+(3.031)+(9.003), (I-302)+(3.031)+(9.004), (I-302)+(3.031)+(9.005), (I-302)+(3.031)+(9.006), (I-302)+(3.031)+(9.007), (I-302)+(3.031)+(9.008), (I-302)+(3.031)+(9.009), (I-302)+(3.031)+(14.001), (I-302)+(3.031)+(14.002), (I-302)+(3.031)+(15.008), (I-302)+(3.031)+(15.011), (I-302)+(3.031)+(15.012), (I-302)+(3.031)+(15.016), (I-302)+(3.031)+(15.025), (I-302)+(3.031)+(15.027), (I-302)+(3.031)+(15.047), (I-302)+(3.031)+(15.063), (I-302)+(3.031)+(15.064), (I-302)+(3.031)+(16.001), (I-302)+(3.031)+(16.002), (I-302)+(3.031)+(16.003), (I-302)+(3.031)+(16.004), (I-302)+(3.031)+(16.005), (I-302)+(3.031)+(16.006), (I-302)+(3.031)+(16.007), (I-302)+(3.031)+(16.008), (I-302)+(3.031)+(17.001), (I-302)+(3.031)+(17.002), (I-302)+(3.031)+(17.003), (I-302)+(3.031)+(17.004), (I-302)+(3.031)+(17.005), (I-302)+(3.031)+(17.006), (I-302)+(3.031)+(17.007), (I-302)+(3.031)+(17.008), (I-302)+(3.031)+(17.009), (I-302)+(3.031)+(17.010), (I-302)+(3.031)+(17.011), (I-302)+(3.031)+(17.012), (I-302)+(3.031)+(18.001), (I-302)+(5.001)+(9.001), (I-302)+(5.001)+(9.002), (I-302)+(5.001)+(9.003), (I-302)+(5.001)+(9.004), (I-302)+(5.001)+(9.005), (I-302)+(5.001)+(9.006), (I-302)+(5.001)+(9.007), (I-302)+(5.001)+(9.008), (I-302)+(5.001)+(9.009), (I-302)+(5.001)+(15.012), (I-302)+(5.001)+(15.016), (I-302)+(5.001)+(15.025), (I-302)+(5.001)+(15.027), (I-302)+(5.001)+(15.047), (I-302)+(5.001)+(15.063), (I-302)+(5.001)+(15.064), (I-302)+(5.002)+(9.001), (I-302)+(5.002)+(9.002), (I-302)+(5.002)+(9.003), (I-302)+(5.002)+(9.004), (I-302)+(5.002)+(9.005), (I-302)+(5.002)+(9.006), (I-302)+(5.002)+(9.007), (I-302)+(5.002)+(9.008), (I-302)+(5.002)+(9.009), (I-302)+(5.002)+(15.012), (I-302)+(5.002)+(15.016), (I-302)+(5.002)+(15.025), (I-302)+(5.002)+(15.027), (I-302)+(5.002)+(15.047), (I-302)+(5.002)+(15.063), (I-302)+(5.002)+(15.064), (I-302)+(5.003)+(9.001), (I-302)+(5.003)+(9.002), (I-302)+(5.003)+(9.003), (I-302)+(5.003)+(9.004), (I-302)+(5.003)+(9.005), (I-302)+(5.003)+(9.006), (I-302)+(5.003)+(9.007), (I-302)+(5.003)+(9.008), (I-302)+(5.003)+(9.009), (I-302)+(5.003)+(15.012), (I-302)+(5.003)+(15.016), (I-302)+(5.003)+(15.025), (I-302)+(5.003)+(15.027), (I-302)+(5.003)+(15.047), (I-302)+(5.003)+(15.063), (I-302)+(5.003)+(15.064), (I-302)+(5.004)+(9.001), (I-302)+(5.004)+(9.002), (I-302)+(5.004)+(9.003), (I-302)+(5.004)+(9.004), (I-302)+(5.004)+(9.005), (I-302)+(5.004)+(9.006), (I-302)+(5.004)+(9.007), (I-302)+(5.004)+(9.008), (I-302)+(5.004)+(9.009), (I-302)+(5.004)+(15.012), (I-302)+(5.004)+(15.016), (I-302)+(5.004)+(15.025), (I-302)+(5.004)+(15.027), (I-302)+(5.004)+(15.047), (I-302)+(5.004)+(15.063), (I-302)+(5.004)+(15.064), (I-302)+(5.005)+(9.001), (I-302)+(5.005)+(9.002), (I-302)+(5.005)+(9.003), (I-302)+(5.005)+(9.004), (I-302)+(5.005)+(9.005), (I-302)+(5.005)+(9.006), (I-302)+(5.005)+(9.007), (I-302)+(5.005)+(9.008), (I-302)+(5.005)+(9.009), (I-302)+(5.005)+(15.012), (I-302)+(5.005)+(15.016), (I-302)+(5.005)+(15.025), (I-302)+(5.005)+(15.027), (I-302)+(5.005)+(15.047), (I-302)+(5.005)+(15.063), (I-302)+(5.005)+(15.064), (I-302)+(5.006)+(9.001), (I-302)+(5.006)+(9.002), (I-302)+(5.006)+(9.003), (I-302)+(5.006)+(9.004), (I-302)+(5.006)+(9.005), (I-302)+(5.006)+(9.006), (I-302)+(5.006)+(9.007), (I-302)+(5.006)+(9.008), (I-302)+(5.006)+(9.009), (I-302)+(5.006)+(15.012), (I-302)+(5.006)+(15.016), (I-302)+(5.006)+(15.025), (I-302)+(5.006)+(15.027), (I-302)+(5.006)+(15.047), (I-302)+(5.006)+(15.063), (I-302)+(5.006)+(15.064), (I-302)+(5.007)+(9.001), (I-302)+(5.007)+(9.002), (I-302)+(5.007)+(9.003), (I-302)+(5.007)+(9.004), (I-302)+(5.007)+(9.005), (I-302)+(5.007)+(9.006), (I-302)+(5.007)+(9.007), (I-302)+(5.007)+(9.008), (I-302)+(5.007)+(9.009), (I-302)+(5.007)+(15.012), (I-302)+(5.007)+(15.016), (I-302)+(5.007)+(15.025), (I-302)+(5.007)+(15.027), (I-302)+(5.007)+(15.047), (I-302)+(5.007)+(15.063), (I-302)+(5.007)+(15.064), (I-302)+(5.008)+(9.001), (I-302)+(5.008)+(9.002), (I-302)+(5.008)+(9.003), (I-302)+(5.008)+(9.004), (I-302)+(5.008)+(9.005), (I-302)+(5.008)+(9.006), (I-302)+(5.008)+(9.007), (I-302)+(5.008)+(9.008), (I-302)+(5.008)+(9.009), (I-302)+(5.008)+(15.012), (I-302)+(5.008)+(15.016), (I-302)+(5.008)+(15.025), (I-302)+(5.008)+(15.027), (I-302)+(5.008)+(15.047), (I-302)+(5.008)+(15.063), (I-302)+(5.008)+(15.064), (I-302)+(5.009)+(9.001), (I-302)+(5.009)+(9.002), (I-302)+(5.009)+(9.003), (I-302)+(5.009)+(9.004), (I-302)+(5.009)+(9.005), (I-302)+(5.009)+(9.006), (I-302)+(5.009)+(9.007), (I-302)+(5.009)+(9.008), (I-302)+(5.009)+(9.009), (I-302)+(5.009)+(15.012), (I-302)+(5.009)+(15.016), (I-302)+(5.009)+(15.025), (I-302)+(5.009)+(15.027), (I-302)+(5.009)+(15.047), (I-302)+(5.009)+(15.063), (I-302)+(5.009)+(15.064), (I-302)+(5.010)+(9.001), (I-302)+(5.010)+(9.002), (I-302)+(5.010)+(9.003), (I-302)+(5.010)+(9.004), (I-302)+(5.010)+(9.005), (I-302)+(5.010)+(9.006), (I-302)+(5.010)+(9.007), (I-302)+(5.010)+(9.008), (I-302)+(5.010)+(9.009), (I-302)+(5.010)+(15.012), (I-302)+(5.010)+(15.016), (I-302)+(5.010)+(15.025), (I-302)+(5.010)+(15.027), (I-302)+(5.010)+(15.047), (I-302)+(5.010)+(15.063), (I-302)+(5.010)+(15.064), (I-302)+(5.011)+(9.001), (I-302)+(5.011)+(9.002), (I-302)+(5.011)+(9.003), (I-302)+(5.011)+(9.004), (I-302)+(5.011)+(9.005), (I-302)+(5.011)+(9.006), (I-302)+(5.011)+(9.007), (I-302)+(5.011)+(9.008), (I-302)+(5.011)+(9.009), (I-302)+(5.011)+(15.012), (I-302)+(5.011)+(15.016), (I-302)+(5.011)+(15.025), (I-302)+(5.011)+(15.027), (I-302)+(5.011)+(15.047), (I-302)+(5.011)+(15.063), (I-302)+(5.011)+(15.064), (I-302)+(5.012)+(9.001), (I-302)+(5.012)+(9.002), (I-302)+(5.012)+(9.003), (I-302)+(5.012)+(9.004), (I-302)+(5.012)+(9.005), (I-302)+(5.012)+(9.006), (I-302)+(5.012)+(9.007), (I-302)+(5.012)+(9.008), (I-302)+(5.012)+(9.009), (I-302)+(5.012)+(15.012), (I-302)+(5.012)+(15.016), (I-302)+(5.012)+(15.025), (I-302)+(5.012)+(15.027), (I-302)+(5.012)+(15.047), (I-302)+(5.012)+(15.063), (I-302)+(5.012)+(15.064), (I-302)+(5.013)+(9.001), (I-302)+(5.013)+(9.002), (I-302)+(5.013)+(9.003), (I-302)+(5.013)+(9.004), (I-302)+(5.013)+(9.005), (I-302)+(5.013)+(9.006), (I-302)+(5.013)+(9.007), (I-302)+(5.013)+(9.008), (I-302)+(5.013)+(9.009), (I-302)+(5.013)+(15.012), (I-302)+(5.013)+(15.016), (I-302)+(5.013)+(15.025), (I-302)+(5.013)+(15.027), (I-302)+(5.013)+(15.047), (I-302)+(5.013)+(15.063), (I-302)+(5.013)+(15.064), (I-302)+(5.014)+(9.001), (I-302)+(5.014)+(9.002), (I-302)+(5.014)+(9.003), (I-302)+(5.014)+(9.004), (I-302)+(5.014)+(9.005), (I-302)+(5.014)+(9.006), (I-302)+(5.014)+(9.007), (I-302)+(5.014)+(9.008), (I-302)+(5.014)+(9.009), (I-302)+(5.014)+(15.012), (I-302)+(5.014)+(15.016), (I-302)+(5.014)+(15.025), (I-302)+(5.014)+(15.027), (I-302)+(5.014)+(15.047), (I-302)+(5.014)+(15.063), (I-302)+(5.014)+(15.064), (I-302)+(5.015)+(9.001), (I-302)+(5.015)+(9.002), (I-302)+(5.015)+(9.003), (I-302)+(5.015)+(9.004), (I-302)+(5.015)+(9.005), (I-302)+(5.015)+(9.006), (I-302)+(5.015)+(9.007), (I-302)+(5.015)+(9.008), (I-302)+(5.015)+(9.009), (I-302)+(5.015)+(15.012), (I-302)+(5.015)+(15.016), (I-302)+(5.015)+(15.025), (I-302)+(5.015)+(15.027), (I-302)+(5.015)+(15.047), (I-302)+(5.015)+(15.063), (I-302)+(5.015)+(15.064), (I-302)+(5.016)+(9.001), (I-302)+(5.016)+(9.002), (I-302)+(5.016)+(9.003), (I-302)+(5.016)+(9.004), (I-302)+(5.016)+(9.005), (I-302)+(5.016)+(9.006), (I-302)+(5.016)+(9.007), (I-302)+(5.016)+(9.008), (I-302)+(5.016)+(9.009), (I-302)+(5.016)+(15.012), (I-302)+(5.016)+(15.016), (I-302)+(5.016)+(15.025), (I-302)+(5.016)+(15.027), (I-302)+(5.016)+(15.047), (I-302)+(5.016)+(15.063), (I-302)+(5.016)+(15.064), (I-302)+(5.017)+(9.001), (I-302)+(5.017)+(9.002), (I-302)+(5.017)+(9.003), (I-302)+(5.017)+(9.004), (I-302)+(5.017)+(9.005), (I-302)+(5.017)+(9.006), (I-302)+(5.017)+(9.007), (I-302)+(5.017)+(9.008), (I-302)+(5.017)+(9.009), (I-302)+(5.017)+(15.012), (I-302)+(5.017)+(15.016), (I-302)+(5.017)+(15.025), (I-302)+(5.017)+(15.027), (I-302)+(5.017)+(15.047), (I-302)+(5.017)+(15.063), (I-302)+(5.017)+(15.064), (I-302)+(5.018)+(9.001), (I-302)+(5.018)+(9.002), (I-302)+(5.018)+(9.003), (I-302)+(5.018)+(9.004), (I-302)+(5.018)+(9.005), (I-302)+(5.018)+(9.006), (I-302)+(5.018)+(9.007), (I-302)+(5.018)+(9.008), (I-302)+(5.018)+(9.009), (I-302)+(5.018)+(15.012), (I-302)+(5.018)+(15.016), (I-302)+(5.018)+(15.025), (I-302)+(5.018)+(15.027), (I-302)+(5.018)+(15.047), (I-302)+(5.018)+(15.063), (I-302)+(5.018)+(15.064), (I-302)+(5.019)+(9.001), (I-302)+(5.019)+(9.002), (I-302)+(5.019)+(9.003), (I-302)+(5.019)+(9.004), (I-302)+(5.019)+(9.005), (I-302)+(5.019)+(9.006), (I-302)+(5.019)+(9.007), (I-302)+(5.019)+(9.008), (I-302)+(5.019)+(9.009), (I-302)+(5.019)+(15.012), (I-302)+(5.019)+(15.016), (I-302)+(5.019)+(15.025), (I-302)+(5.019)+(15.027), (I-302)+(5.019)+(15.047), (I-302)+(5.019)+(15.063), (I-302)+(5.019)+(15.064), (I-302)+(5.020)+(9.001), (I-302)+(5.020)+(9.002), (I-302)+(5.020)+(9.003), (I-302)+(5.020)+(9.004), (I-302)+(5.020)+(9.005), (I-302)+(5.020)+(9.006), (I-302)+(5.020)+(9.007), (I-302)+(5.020)+(9.008), (I-302)+(5.020)+(9.009), (I-302)+(5.020)+(15.012), (I-302)+(5.020)+(15.016), (I-302)+(5.020)+(15.025), (I-302)+(5.020)+(15.027), (I-302)+(5.020)+(15.047), (I-302)+(5.020)+(15.063), (I-302)+(5.020)+(15.064), (I-302)+(5.021)+(9.001), (I-302)+(5.021)+(9.002), (I-302)+(5.021)+(9.003), (I-302)+(5.021)+(9.004), (I-302)+(5.021)+(9.005), (I-302)+(5.021)+(9.006), (I-302)+(5.021)+(9.007), (I-302)+(5.021)+(9.008), (I-302)+(5.021)+(9.009), (I-302)+(5.021)+(15.012), (I-302)+(5.021)+(15.016), (I-302)+(5.021)+(15.025), (I-302)+(5.021)+(15.027), (I-302)+(5.021)+(15.047), (I-302)+(5.021)+(15.063), (I-302)+(5.021)+(15.064), (I-302)+(5.022)+(9.001), (I-302)+(5.022)+(9.002), (I-302)+(5.022)+(9.003), (I-302)+(5.022)+(9.004), (I-302)+(5.022)+(9.005), (I-302)+(5.022)+(9.006), (I-302)+(5.022)+(9.007), (I-302)+(5.022)+(9.008), (I-302)+(5.022)+(9.009), (I-302)+(5.022)+(15.012), (I-302)+(5.022)+(15.016), (I-302)+(5.022)+(15.025), (I-302)+(5.022)+(15.027), (I-302)+(5.022)+(15.047), (I-302)+(5.022)+(15.063), (I-302)+(5.022)+(15.064), (I-302)+(5.023)+(9.001), (I-302)+(5.023)+(9.002), (I-302)+(5.023)+(9.003), (I-302)+(5.023)+(9.004), (I-302)+(5.023)+(9.005), (I-302)+(5.023)+(9.006), (I-302)+(5.023)+(9.007), (I-302)+(5.023)+(9.008), (I-302)+(5.023)+(9.009), (I-302)+(5.023)+(15.012), (I-302)+(5.023)+(15.016), (I-302)+(5.023)+(15.025), (I-302)+(5.023)+(15.027), (I-302)+(5.023)+(15.047), (I-302)+(5.023)+(15.063), (I-302)+(5.023)+(15.064).

If Two Compounds (B) are Present in the Combinations According to the Invention, More Preferred Compound Combinations are Selected from the Group (G1-C1) Consisting of the Following Mixtures:

(I-052)+(1.001)+(1.002), (I-052)+(1.001)+(1.003), (I-052)+(1.001)+(1.004), (I-052)+(1.001)+(1.005), (I-052)+(1.001)+(1.006), (I-052)+(1.001)+(1.007), (I-052)+(1.001)+(1.010), (I-052)+(1.001)+(1.011), (I-052)+(1.001)+(1.012), (I-052)+(1.001)+(1.013), (I-052)+(1.001)+(1.017), (I-052)+(1.001)+(1.018), (I-052)+(1.001)+(1.020), (I-052)+(1.001)+(1.021), (I-052)+(1.001)+(1.026), (I-052)+(1.001)+(1.027), (I-052)+(1.001)+(1.055), (I-052)+(1.001)+(1.059), (I-052)+(1.001)+(1.092), (I-052)+(1.001)+(2.001), (I-052)+(1.001)+(2.002), (I-052)+(1.001)+(2.003), (I-052)+(1.001)+(2.005), (I-052)+(1.001)+(2.007), (I-052)+(1.001)+(2.009), (I-052)+(1.001)+(2.010), (I-052)+(1.001)+(2.011), (I-052)+(1.001)+(2.012), (I-052)+(1.001)+(2.013), (I-052)+(1.001)+(2.014), (I-052)+(1.001)+(2.015), (I-052)+(1.001)+(2.016), (I-052)+(1.001)+(2.017), (I-052)+(1.001)+(2.018), (I-052)+(1.001)+(2.019), (I-052)+(1.001)+(2.021), (I-052)+(1.001)+(2.028), (I-052)+(1.001)+(2.030), (I-052)+(1.001)+(2.038), (I-052)+(1.001)+(3.003), (I-052)+(1.001)+(3.007), (I-052)+(1.001)+(3.012), (I-052)+(1.001)+(3.013), (I-052)+(1.001)+(3.016), (I-052)+(1.001)+(3.017), (I-052)+(1.001)+(3.020), (I-052)+(1.001)+(3.025), (I-052)+(1.001)+(3.026), (I-052)+(1.001)+(3.030), (I-052)+(1.001)+(3.031), (I-052)+(1.001)+(5.003), (I-052)+(1.001)+(5.004), (I-052)+(1.001)+(5.005), (I-052)+(1.001)+(5.008), (I-052)+(1.001)+(5.009), (I-052)+(1.001)+(5.011), (I-052)+(1.001)+(5.012), (I-052)+(1.001)+(5.013), (I-052)+(1.001)+(5.015), (I-052)+(1.001)+(5.018), (I-052)+(1.001)+(5.019), (I-052)+(1.001)+(6.002), (I-052)+(1.001)+(7.001), (I-052)+(1.001)+(7.005), (I-052)+(1.001)+(9.002), (I-052)+(1.001)+(9.004), (I-052)+(1.001)+(14.001), (I-052)+(1.001)+(14.002), (I-052)+(1.001)+(15.008), (I-052)+(1.001)+(15.011), (I-052)+(1.001)+(15.012), (I-052)+(1.001)+(15.016), (I-052)+(1.001)+(15.025), (I-052)+(1.001)+(15.027), (I-052)+(1.001)+(15.047), (I-052)+(1.001)+(15.063), (I-052)+(1.001)+(15.064), (I-052)+(1.001)+(16.001), (I-052)+(1.001)+(16.005), (I-052)+(1.001)+(17.001), (I-052)+(1.001)+(17.002), (I-052)+(1.001)+(17.003), (I-052)+(1.001)+(17.008), (I-052)+(1.001)+(18.001), (I-052)+(1.002)+(1.001), (I-052)+(1.002)+(1.003), (I-052)+(1.002)+(1.004), (I-052)+(1.002)+(1.005), (I-052)+(1.002)+(1.006), (I-052)+(1.002)+(1.007), (I-052)+(1.002)+(1.010), (I-052)+(1.002)+(1.011), (I-052)+(1.002)+(1.012), (I-052)+(1.002)+(1.013), (I-052)+(1.002)+(1.017), (I-052)+(1.002)+(1.018), (I-052)+(1.002)+(1.020), (I-052)+(1.002)+(1.021), (I-052)+(1.002)+(1.026), (I-052)+(1.002)+(1.027), (I-052)+(1.002)+(1.055), (I-052)+(1.002)+(1.059), (I-052)+(1.002)+(1.092), (I-052)+(1.002)+(2.001), (I-052)+(1.002)+(2.002), (I-052)+(1.002)+(2.003), (I-052)+(1.002)+(2.005), (I-052)+(1.002)+(2.007), (I-052)+(1.002)+(2.009), (I-052)+(1.002)+(2.010), (I-052)+(1.002)+(2.011), (I-052)+(1.002)+(2.012), (I-052)+(1.002)+(2.013), (I-052)+(1.002)+(2.014), (I-052)+(1.002)+(2.015), (I-052)+(1.002)+(2.016), (I-052)+(1.002)+(2.017), (I-052)+(1.002)+(2.018), (I-052)+(1.002)+(2.019), (I-052)+(1.002)+(2.021), (I-052)+(1.002)+(2.028), (I-052)+(1.002)+(2.030), (I-052)+(1.002)+(2.038), (I-052)+(1.002)+(3.003), (I-052)+(1.002)+(3.007), (I-052)+(1.002)+(3.012), (I-052)+(1.002)+(3.013), (I-052)+(1.002)+(3.016), (I-052)+(1.002)+(3.017), (I-052)+(1.002)+(3.020), (I-052)+(1.002)+(3.025), (I-052)+(1.002)+(3.026), (I-052)+(1.002)+(3.030), (I-052)+(1.002)+(3.031), (I-052)+(1.002)+(5.003), (I-052)+(1.002)+(5.004), (I-052)+(1.002)+(5.005), (I-052)+(1.002)+(5.008), (I-052)+(1.002)+(5.009), (I-052)+(1.002)+(5.011), (I-052)+(1.002)+(5.012), (I-052)+(1.002)+(5.013), (I-052)+(1.002)+(5.015), (I-052)+(1.002)+(5.018), (I-052)+(1.002)+(5.019), (I-052)+(1.002)+(6.002), (I-052)+(1.002)+(7.001), (I-052)+(1.002)+(7.005), (I-052)+(1.002)+(9.002), (I-052)+(1.002)+(9.004), (I-052)+(1.002)+(14.001), (I-052)+(1.002)+(14.002), (I-052)+(1.002)+(15.008), (I-052)+(1.002)+(15.011), (I-052)+(1.002)+(15.012), (I-052)+(1.002)+(15.016), (I-052)+(1.002)+(15.025), (I-052)+(1.002)+(15.027), (I-052)+(1.002)+(15.047), (I-052)+(1.002)+(15.063), (I-052)+(1.002)+(15.064), (I-052)+(1.002)+(16.001), (I-052)+(1.002)+(16.005), (I-052)+(1.002)+(17.001), (I-052)+(1.002)+(17.002), (I-052)+(1.002)+(17.003), (I-052)+(1.002)+(17.008), (I-052)+(1.002)+(18.001), (I-052)+(1.003)+(1.001), (I-052)+(1.003)+(1.002), (I-052)+(1.003)+(1.004), (I-052)+(1.003)+(1.005), (I-052)+(1.003)+(1.006), (I-052)+(1.003)+(1.007), (I-052)+(1.003)+(1.010), (I-052)+(1.003)+(1.011), (I-052)+(1.003)+(1.012), (I-052)+(1.003)+(1.013), (I-052)+(1.003)+(1.017), (I-052)+(1.003)+(1.018), (I-052)+(1.003)+(1.020), (I-052)+(1.003)+(1.021), (I-052)+(1.003)+(1.026), (I-052)+(1.003)+(1.027), (I-052)+(1.003)+(1.055), (I-052)+(1.003)+(1.059), (I-052)+(1.003)+(1.092), (I-052)+(1.003)+(2.001), (I-052)+(1.003)+(2.002), (I-052)+(1.003)+(2.003), (I-052)+(1.003)+(2.005), (I-052)+(1.003)+(2.007), (I-052)+(1.003)+(2.009), (I-052)+(1.003)+(2.010), (I-052)+(1.003)+(2.011), (I-052)+(1.003)+(2.012), (I-052)+(1.003)+(2.013), (I-052)+(1.003)+(2.014), (I-052)+(1.003)+(2.015), (I-052)+(1.003)+(2.016), (I-052)+(1.003)+(2.017), (I-052)+(1.003)+(2.018), (1-052)+(1.003)+(2.019), (I-052)+(1.003)+(2.021), (I-052)+(1.003)+(2.028), (I-052)+(1.003)+(2.030), (I-052)+(1.003)+(2.038), (I-052)+(1.003)+(3.003), (I-052)+(1.003)+(3.007), (I-052)+(1.003)+(3.012), (I-052)+(1.003)+(3.013), (I-052)+(1.003)+(3.016), (I-052)+(1.003)+(3.017), (I-052)+(1.003)+(3.020), (I-052)+(1.003)+(3.025), (I-052)+(1.003)+(3.026), (I-052)+(1.003)+(3.030), (I-052)+(1.003)+(3.031), (I-052)+(1.003)+(5.003), (I-052)+(1.003)+(5.004), (I-052)+(1.003)+(5.005), (I-052)+(1.003)+(5.008), (I-052)+(1.003)+(5.009), (I-052)+(1.003)+(5.011), (I-052)+(1.003)+(5.012), (I-052)+(1.003)+(5.013), (I-052)+(1.003)+(5.015), (I-052)+(1.003)+(5.018), (I-052)+(1.003)+(5.019), (I-052)+(1.003)+(6.002), (I-052)+(1.003)+(7.001), (I-052)+(1.003)+(7.005), (I-052)+(1.003)+(9.002), (I-052)+(1.003)+(9.004), (I-052)+(1.003)+(14.001), (I-052)+(1.003)+(14.002), (I-052)+(1.003)+(15.008), (I-052)+(1.003)+(15.011), (I-052)+(1.003)+(15.012), (I-052)+(1.003)+(15.016), (I-052)+(1.003)+(15.025), (I-052)+(1.003)+(15.027), (I-052)+(1.003)+(15.047), (I-052)+(1.003)+(15.063), (I-052)+(1.003)+(15.064), (I-052)+(1.003)+(16.001), (I-052)+(1.003)+(16.005), (I-052)+(1.003)+(17.001), (I-052)+(1.003)+(17.002), (I-052)+(1.003)+(17.003), (I-052)+(1.003)+(17.008), (I-052)+(1.003)+(18.001), (I-052)+(1.004)+(1.001), (I-052)+(1.004)+(1.002), (I-052)+(1.004)+(1.003), (I-052)+(1.004)+(1.005), (I-052)+(1.004)+(1.006), (I-052)+(1.004)+(1.007), (I-052)+(1.004)+(1.010), (I-052)+(1.004)+(1.011), (I-052)+(1.004)+(1.012), (I-052)+(1.004)+(1.013), (I-052)+(1.004)+(1.017), (I-052)+(1.004)+(1.018), (I-052)+(1.004)+(1.020), (I-052)+(1.004)+(1.021), (I-052)+(1.004)+(1.026), (I-052)+(1.004)+(1.027), (I-052)+(1.004)+(1.055), (I-052)+(1.004)+(1.059), (I-052)+(1.004)+(1.092), (I-052)+(1.004)+(2.001), (I-052)+(1.004)+(2.002), (I-052)+(1.004)+(2.003), (I-052)+(1.004)+(2.005), (I-052)+(1.004)+(2.007), (I-052)+(1.004)+(2.009), (I-052)+(1.004)+(2.010), (I-052)+(1.004)+(2.011), (I-052)+(1.004)+(2.012), (I-052)+(1.004)+(2.013), (I-052)+(1.004)+(2.014), (I-052)+(1.004)+(2.015), (I-052)+(1.004)+(2.016), (I-052)+(1.004)+(2.017), (I-052)+(1.004)+(2.018), (I-052)+(1.004)+(2.019), (I-052)+(1.004)+(2.021), (I-052)+(1.004)+(2.028), (I-052)+(1.004)+(2.030), (I-052)+(1.004)+(2.038), (I-052)+(1.004)+(3.003), (I-052)+(1.004)+(3.007), (I-052)+(1.004)+(3.012), (I-052)+(1.004)+(3.013), (I-052)+(1.004)+(3.016), (I-052)+(1.004)+(3.017), (I-052)+(1.004)+(3.020), (I-052)+(1.004)+(3.025), (I-052)+(1.004)+(3.026), (I-052)+(1.004)+(3.030), (I-052)+(1.004)+(3.031), (I-052)+(1.004)+(5.003), (I-052)+(1.004)+(5.004), (I-052)+(1.004)+(5.005), (I-052)+(1.004)+(5.008), (I-052)+(1.004)+(5.009), (I-052)+(1.004)+(5.011), (I-052)+(1.004)+(5.012), (I-052)+(1.004)+(5.013), (I-052)+(1.004)+(5.015), (I-052)+(1.004)+(5.018), (I-052)+(1.004)+(5.019), (I-052)+(1.004)+(6.002), (I-052)+(1.004)+(7.001), (I-052)+(1.004)+(7.005), (I-052)+(1.004)+(9.002), (I-052)+(1.004)+(9.004), (I-052)+(1.004)+(14.001), (I-052)+(1.004)+(14.002), (I-052)+(1.004)+(15.008), (I-052)+(1.004)+(15.011), (I-052)+(1.004)+(15.012), (I-052)+(1.004)+(15.016), (I-052)+(1.004)+(15.025), (I-052)+(1.004)+(15.027), (I-052)+(1.004)+(15.047), (I-052)+(1.004)+(15.063), (I-052)+(1.004)+(15.064), (I-052)+(1.004)+(16.001), (I-052)+(1.004)+(16.005), (I-052)+(1.004)+(17.001), (I-052)+(1.004)+(17.002), (I-052)+(1.004)+(17.003), (I-052)+(1.004)+(17.008), (I-052)+(1.004)+(18.001), (I-052)+(1.005)+(1.001), (I-052)+(1.005)+(1.002), (I-052)+(1.005)+(1.003), (I-052)+(1.005)+(1.004), (I-052)+(1.005)+(1.006), (I-052)+(1.005)+(1.007), (I-052)+(1.005)+(1.010), (I-052)+(1.005)+(1.011), (I-052)+(1.005)+(1.012), (I-052)+(1.005)+(1.013), (I-052)+(1.005)+(1.017), (I-052)+(1.005)+(1.018), (I-052)+(1.005)+(1.020), (I-052)+(1.005)+(1.021), (I-052)+(1.005)+(1.026), (I-052)+(1.005)+(1.027), (I-052)+(1.005)+(1.055), (I-052)+(1.005)+(1.059), (I-052)+(1.005)+(1.092), (I-052)+(1.005)+(2.001), (I-052)+(1.005)+(2.002), (I-052)+(1.005)+(2.003), (I-052)+(1.005)+(2.005), (I-052)+(1.005)+(2.007), (I-052)+(1.005)+(2.009), (I-052)+(1.005)+(2.010), (I-052)+(1.005)+(2.011), (I-052)+(1.005)+(2.012), (I-052)+(1.005)+(2.013), (I-052)+(1.005)+(2.014), (I-052)+(1.005)+(2.015), (I-052)+(1.005)+(2.016), (I-052)+(1.005)+(2.017), (I-052)+(1.005)+(2.018), (I-052)+(1.005)+(2.019), (I-052)+(1.005)+(2.021), (I-052)+(1.005)+(2.028), (I-052)+(1.005)+(2.030), (I-052)+(1.005)+(2.038), (I-052)+(1.005)+(3.003), (I-052)+(1.005)+(3.007), (I-052)+(1.005)+(3.012), (I-052)+(1.005)+(3.013), (I-052)+(1.005)+(3.016), (I-052)+(1.005)+(3.017), (I-052)+(1.005)+(3.020), (I-052)+(1.005)+(3.025), (I-052)+(1.005)+(3.026), (I-052)+(1.005)+(3.030), (I-052)+(1.005)+(3.031), (I-052)+(1.005)+(5.003), (I-052)+(1.005)+(5.004), (I-052)+(1.005)+(5.005), (I-052)+(1.005)+(5.008), (I-052)+(1.005)+(5.009), (I-052)+(1.005)+(5.011), (I-052)+(1.005)+(5.012), (I-052)+(1.005)+(5.013), (I-052)+(1.005)+(5.015), (I-052)+(1.005)+(5.018), (I-052)+(1.005)+(5.019), (I-052)+(1.005)+(6.002), (I-052)+(1.005)+(7.001), (I-052)+(1.005)+(7.005), (I-052)+(1.005)+(9.002), (I-052)+(1.005)+(9.004), (I-052)+(1.005)+(14.001), (I-052)+(1.005)+(14.002), (I-052)+(1.005)+(15.008), (I-052)+(1.005)+(15.011), (I-052)+(1.005)+(15.012), (I-052)+(1.005)+(15.016), (I-052)+(1.005)+(15.025), (I-052)+(1.005)+(15.027), (I-052)+(1.005)+(15.047), (I-052)+(1.005)+(15.063), (I-052)+(1.005)+(15.064), (I-052)+(1.005)+(16.001), (I-052)+(1.005)+(16.005), (I-052)+(1.005)+(17.001), (I-052)+(1.005)+(17.002), (I-052)+(1.005)+(17.003), (I-052)+(1.005)+(17.008), (I-052)+(1.005)+(18.001), (I-052)+(1.006)+(1.001), (I-052)+(1.006)+(1.002), (I-052)+(1.006)+(1.003), (I-052)+(1.006)+(1.004), (I-052)+(1.006)+(1.005), (I-052)+(1.006)+(1.007), (I-052)+(1.006)+(1.010), (I-052)+(1.006)+(1.011), (I-052)+(1.006)+(1.012), (I-052)+(1.006)+(1.013), (I-052)+(1.006)+(1.017), (I-052)+(1.006)+(1.018), (I-052)+(1.006)+(1.020), (I-052)+(1.006)+(1.021), (I-052)+(1.006)+(1.026), (I-052)+(1.006)+(1.027), (I-052)+(1.006)+(1.055), (I-052)+(1.006)+(1.059), (I-052)+(1.006)+(1.092), (I-052)+(1.006)+(2.001), (I-052)+(1.006)+(2.002), (I-052)+(1.006)+(2.003), (I-052)+(1.006)+(2.005), (I-052)+(1.006)+(2.007), (I-052)+(1.006)+(2.009), (I-052)+(1.006)+(2.010), (I-052)+(1.006)+(2.011), (I-052)+(1.006)+(2.012), (I-052)+(1.006)+(2.013), (I-052)+(1.006)+(2.014), (I-052)+(1.006)+(2.015), (I-052)+(1.006)+(2.016), (I-052)+(1.006)+(2.017), (I-052)+(1.006)+(2.018), (I-052)+(1.006)+(2.019), (I-052)+(1.006)+(2.021), (I-052)+(1.006)+(2.028), (I-052)+(1.006)+(2.030), (I-052)+(1.006)+(2.038), (I-052)+(1.006)+(3.003), (I-052)+(1.006)+(3.007), (I-052)+(1.006)+(3.012), (I-052)+(1.006)+(3.013), (I-052)+(1.006)+(3.016), (I-052)+(1.006)+(3.017), (I-052)+(1.006)+(3.020), (I-052)+(1.006)+(3.025), (I-052)+(1.006)+(3.026), (I-052)+(1.006)+(3.030), (I-052)+(1.006)+(3.031), (I-052)+(1.006)+(5.003), (I-052)+(1.006)+(5.004), (I-052)+(1.006)+(5.005), (1-052)+(1.006)+(5.008), (I-052)+(1.006)+(5.009), (I-052)+(1.006)+(5.011), (I-052)+(1.006)+(5.012), (I-052)+(1.006)+(5.013), (I-052)+(1.006)+(5.015), (I-052)+(1.006)+(5.018), (I-052)+(1.006)+(5.019), (I-052)+(1.006)+(6.002), (I-052)+(1.006)+(7.001), (I-052)+(1.006)+(7.005), (I-052)+(1.006)+(9.002), (I-052)+(1.006)+(9.004), (I-052)+(1.006)+(14.001), (I-052)+(1.006)+(14.002), (I-052)+(1.006)+(15.008), (I-052)+(1.006)+(15.011), (I-052)+(1.006)+(15.012), (I-052)+(1.006)+(15.016), (I-052)+(1.006)+(15.025), (I-052)+(1.006)+(15.027), (I-052)+(1.006)+(15.047), (I-052)+(1.006)+(15.063), (I-052)+(1.006)+(15.064), (I-052)+(1.006)+(16.001), (I-052)+(1.006)+(16.005), (I-052)+(1.006)+(17.001), (I-052)+(1.006)+(17.002), (I-052)+(1.006)+(17.003), (I-052)+(1.006)+(17.008), (I-052)+(1.006)+(18.001), (I-052)+(1.007)+(1.001), (I-052)+(1.007)+(1.002), (I-052)+(1.007)+(1.003), (I-052)+(1.007)+(1.004), (I-052)+(1.007)+(1.005), (I-052)+(1.007)+(1.006), (I-052)+(1.007)+(1.010), 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(I-052)+(3.013)+(5.008), (I-052)+(3.013)+(5.009), (I-052)+(3.013)+(5.011), (I-052)+(3.013)+(5.012), (I-052)+(3.013)+(5.013), (I-052)+(3.013)+(5.015), (I-052)+(3.013)+(5.018), (I-052)+(3.013)+(5.019), (I-052)+(3.013)+(6.002), (I-052)+(3.013)+(7.001), (I-052)+(3.013)+(7.005), (I-052)+(3.013)+(9.002), (I-052)+(3.013)+(9.004), (I-052)+(3.013)+(14.001), (I-052)+(3.013)+(14.002), (I-052)+(3.013)+(15.008), (I-052)+(3.013)+(15.011), (I-052)+(3.013)+(15.012), (I-052)+(3.013)+(15.016), (I-052)+(3.013)+(15.025), (I-052)+(3.013)+(15.027), (I-052)+(3.013)+(15.047), (I-052)+(3.013)+(15.063), (I-052)+(3.013)+(15.064), (I-052)+(3.013)+(16.001), (I-052)+(3.013)+(16.005), (I-052)+(3.013)+(17.001), (I-052)+(3.013)+(17.002), (I-052)+(3.013)+(17.003), (I-052)+(3.013)+(17.008), (I-052)+(3.013)+(18.001), (I-052)+(3.016)+(3.025), (I-052)+(3.016)+(3.030), (I-052)+(3.016)+(3.031), (I-052)+(3.016)+(5.003), (I-052)+(3.016)+(5.004), (I-052)+(3.016)+(5.005), (I-052)+(3.016)+(5.008), (I-052)+(3.016)+(5.009), (I-052)+(3.016)+(5.011), (I-052)+(3.016)+(5.012), (I-052)+(3.016)+(5.013), (I-052)+(3.016)+(5.015), (I-052)+(3.016)+(5.018), (I-052)+(3.016)+(5.019), (I-052)+(3.016)+(6.002), (I-052)+(3.016)+(7.001), (I-052)+(3.016)+(7.005), (I-052)+(3.016)+(9.002), (I-052)+(3.016)+(9.004), (I-052)+(3.016)+(14.001), (I-052)+(3.016)+(14.002), (I-052)+(3.016)+(15.008), (I-052)+(3.016)+(15.011), (I-052)+(3.016)+(15.012), (I-052)+(3.016)+(15.016), (I-052)+(3.016)+(15.025), (I-052)+(3.016)+(15.027), (I-052)+(3.016)+(15.047), (I-052)+(3.016)+(15.063), (I-052)+(3.016)+(15.064), (I-052)+(3.016)+(16.001), (I-052)+(3.016)+(16.005), (I-052)+(3.016)+(17.001), (I-052)+(3.016)+(17.002), (I-052)+(3.016)+(17.003), (I-052)+(3.016)+(17.008), (I-052)+(3.016)+(18.001), (I-052)+(3.017)+(3.025), (I-052)+(3.017)+(3.030), (I-052)+(3.017)+(3.031), (I-052)+(3.017)+(5.003), (I-052)+(3.017)+(5.004), (I-052)+(3.017)+(5.005), (I-052)+(3.017)+(5.008), (I-052)+(3.017)+(5.009), (I-052)+(3.017)+(5.011), (I-052)+(3.017)+(5.012), (I-052)+(3.017)+(5.013), (I-052)+(3.017)+(5.015), (I-052)+(3.017)+(5.018), (I-052)+(3.017)+(5.019), (I-052)+(3.017)+(6.002), (I-052)+(3.017)+(7.001), (I-052)+(3.017)+(7.005), (I-052)+(3.017)+(9.002), (I-052)+(3.017)+(9.004), (I-052)+(3.017)+(14.001), (I-052)+(3.017)+(14.002), (I-052)+(3.017)+(15.008), (I-052)+(3.017)+(15.011), (I-052)+(3.017)+(15.012), (I-052)+(3.017)+(15.016), (I-052)+(3.017)+(15.025), (I-052)+(3.017)+(15.027), (I-052)+(3.017)+(15.047), (I-052)+(3.017)+(15.063), (I-052)+(3.017)+(15.064), (I-052)+(3.017)+(16.001), (I-052)+(3.017)+(16.005), (I-052)+(3.017)+(17.001), (I-052)+(3.017)+(17.002), (I-052)+(3.017)+(17.003), (I-052)+(3.017)+(17.008), (I-052)+(3.017)+(18.001), (I-052)+(3.020)+(3.025), (I-052)+(3.020)+(3.030), (I-052)+(3.020)+(3.031), (I-052)+(3.020)+(5.003), (I-052)+(3.020)+(5.004), (I-052)+(3.020)+(5.005), (I-052)+(3.020)+(5.008), (I-052)+(3.020)+(5.009), (I-052)+(3.020)+(5.011), (I-052)+(3.020)+(5.012), (I-052)+(3.020)+(5.013), (I-052)+(3.020)+(5.015), (I-052)+(3.020)+(5.018), (I-052)+(3.020)+(5.019), (I-052)+(3.020)+(6.002), (I-052)+(3.020)+(7.001), (I-052)+(3.020)+(7.005), (I-052)+(3.020)+(9.002), (I-052)+(3.020)+(9.004), (I-052)+(3.020)+(14.001), (I-052)+(3.020)+(14.002), (I-052)+(3.020)+(15.008), (I-052)+(3.020)+(15.011), (I-052)+(3.020)+(15.012), (I-052)+(3.020)+(15.016), (I-052)+(3.020)+(15.025), (I-052)+(3.020)+(15.027), (I-052)+(3.020)+(15.047), (I-052)+(3.020)+(15.063), (I-052)+(3.020)+(15.064), (I-052)+(3.020)+(16.001), (I-052)+(3.020)+(16.005), (I-052)+(3.020)+(17.001), (I-052)+(3.020)+(17.002), (I-052)+(3.020)+(17.003), (I-052)+(3.020)+(17.008), (I-052)+(3.020)+(18.001), (I-052)+(3.025)+(3.030), (I-052)+(3.025)+(3.031), (I-052)+(3.025)+(5.003), (I-052)+(3.025)+(5.004), (I-052)+(3.025)+(5.005), (I-052)+(3.025)+(5.008), (I-052)+(3.025)+(5.009), (I-052)+(3.025)+(5.011), (I-052)+(3.025)+(5.012), (I-052)+(3.025)+(5.013), (I-052)+(3.025)+(5.015), (I-052)+(3.025)+(5.018), (I-052)+(3.025)+(5.019), (I-052)+(3.025)+(6.002), (I-052)+(3.025)+(7.001), (I-052)+(3.025)+(7.005), (I-052)+(3.025)+(9.002), (I-052)+(3.025)+(9.004), (I-052)+(3.025)+(14.001), (I-052)+(3.025)+(14.002), (I-052)+(3.025)+(15.008), (I-052)+(3.025)+(15.011), (I-052)+(3.025)+(15.012), (I-052)+(3.025)+(15.016), (I-052)+(3.025)+(15.025), (I-052)+(3.025)+(15.027), (I-052)+(3.025)+(15.047), (I-052)+(3.025)+(15.063), (I-052)+(3.025)+(15.064), (I-052)+(3.025)+(16.001), (I-052)+(3.025)+(16.005), (I-052)+(3.025)+(17.001), (I-052)+(3.025)+(17.002), (I-052)+(3.025)+(17.003), (I-052)+(3.025)+(17.008), (I-052)+(3.025)+(18.001), (I-052)+(3.026)+(3.025), (I-052)+(3.026)+(3.030), (I-052)+(3.026)+(3.031), (I-052)+(3.026)+(5.003), (I-052)+(3.026)+(5.004), (I-052)+(3.026)+(5.005), (I-052)+(3.026)+(5.008), (I-052)+(3.026)+(5.009), (I-052)+(3.026)+(5.011), (I-052)+(3.026)+(5.012), (I-052)+(3.026)+(5.013), (I-052)+(3.026)+(5.015), (I-052)+(3.026)+(5.018), (I-052)+(3.026)+(5.019), (I-052)+(3.026)+(6.002), (I-052)+(3.026)+(7.001), (I-052)+(3.026)+(7.005), (I-052)+(3.026)+(9.002), (I-052)+(3.026)+(9.004), (I-052)+(3.026)+(14.001), (I-052)+(3.026)+(14.002), (I-052)+(3.026)+(15.008), (I-052)+(3.026)+(15.011), (I-052)+(3.026)+(15.012), (I-052)+(3.026)+(15.016), (I-052)+(3.026)+(15.025), (I-052)+(3.026)+(15.027), (I-052)+(3.026)+(15.047), (I-052)+(3.026)+(15.063), (I-052)+(3.026)+(15.064), (I-052)+(3.026)+(16.001), (I-052)+(3.026)+(16.005), (I-052)+(3.026)+(17.001), (I-052)+(3.026)+(17.002), (I-052)+(3.026)+(17.003), (I-052)+(3.026)+(17.008), (I-052)+(3.026)+(18.001), (I-052)+(3.030)+(3.025), (I-052)+(3.030)+(3.031), (I-052)+(3.030)+(5.003), (I-052)+(3.030)+(5.004), (I-052)+(3.030)+(5.005), (I-052)+(3.030)+(5.008), (I-052)+(3.030)+(5.009), (I-052)+(3.030)+(5.011), (I-052)+(3.030)+(5.012), (I-052)+(3.030)+(5.013), (I-052)+(3.030)+(5.015), (I-052)+(3.030)+(5.018), (I-052)+(3.030)+(5.019), (I-052)+(3.030)+(6.002), (I-052)+(3.030)+(7.001), (I-052)+(3.030)+(7.005), (I-052)+(3.030)+(9.002), (I-052)+(3.030)+(9.004), (I-052)+(3.030)+(14.001), (I-052)+(3.030)+(14.002), (I-052)+(3.030)+(15.008), (I-052)+(3.030)+(15.011), (I-052)+(3.030)+(15.012), (I-052)+(3.030)+(15.016), (I-052)+(3.030)+(15.025), (I-052)+(3.030)+(15.027), (I-052)+(3.030)+(15.047), (I-052)+(3.030)+(15.063), (I-052)+(3.030)+(15.064), (I-052)+(3.030)+(16.001), (I-052)+(3.030)+(16.005), (I-052)+(3.030)+(17.001), (I-052)+(3.030)+(17.002), (I-052)+(3.030)+(17.003), (I-052)+(3.030)+(17.008), (I-052)+(3.030)+(18.001), (I-052)+(3.031)+(3.025), (I-052)+(3.031)+(3.030), (I-052)+(3.031)+(5.003), (I-052)+(3.031)+(5.004), (I-052)+(3.031)+(5.005), (I-052)+(3.031)+(5.008), (I-052)+(3.031)+(5.009), (I-052)+(3.031)+(5.011), (I-052)+(3.031)+(5.012), (I-052)+(3.031)+(5.013), (I-052)+(3.031)+(5.015), (I-052)+(3.031)+(5.018), (I-052)+(3.031)+(5.019), (I-052)+(3.031)+(6.002), (I-052)+(3.031)+(7.001), (I-052)+(3.031)+(7.005), (I-052)+(3.031)+(9.002), (I-052)+(3.031)+(9.004), (I-052)+(3.031)+(14.001), (I-052)+(3.031)+(14.002), (I-052)+(3.031)+(15.008), (I-052)+(3.031)+(15.011), (I-052)+(3.031)+(15.012), (I-052)+(3.031)+(15.016), (I-052)+(3.031)+(15.025), (I-052)+(3.031)+(15.027), (I-052)+(3.031)+(15.047), (I-052)+(3.031)+(15.063), (I-052)+(3.031)+(15.064), (I-052)+(3.031)+(16.001), (I-052)+(3.031)+(16.005), (I-052)+(3.031)+(17.001), (I-052)+(3.031)+(17.002), (I-052)+(3.031)+(17.003), (I-052)+(3.031)+(17.008), (I-052)+(3.031)+(18.001), (I-052)+(5.003)+(9.002), (I-052)+(5.003)+(15.012), (I-052)+(5.003)+(15.016), (I-052)+(5.003)+(15.025), (I-052)+(5.003)+(15.027), (I-052)+(5.003)+(15.047), (I-052)+(5.003)+(15.063), (I-052)+(5.003)+(15.064), (I-052)+(5.004)+(9.002), (I-052)+(5.004)+(15.012), (I-052)+(5.004)+(15.016), (I-052)+(5.004)+(15.025), (I-052)+(5.004)+(15.027), (I-052)+(5.004)+(15.047), (I-052)+(5.004)+(15.063), (I-052)+(5.004)+(15.064), (I-052)+(5.005)+(9.002), (I-052)+(5.005)+(15.012), (I-052)+(5.005)+(15.016), (I-052)+(5.005)+(15.025), (I-052)+(5.005)+(15.027), (I-052)+(5.005)+(15.047), (I-052)+(5.005)+(15.063), (I-052)+(5.005)+(15.064), (I-052)+(5.008)+(9.002), (I-052)+(5.008)+(15.012), (I-052)+(5.008)+(15.016), (I-052)+(5.008)+(15.025), (I-052)+(5.008)+(15.027), (I-052)+(5.008)+(15.047), (I-052)+(5.008)+(15.063), (I-052)+(5.008)+(15.064), (I-052)+(5.009)+(9.002), (I-052)+(5.009)+(15.012), (I-052)+(5.009)+(15.016), (I-052)+(5.009)+(15.025), (I-052)+(5.009)+(15.027), (I-052)+(5.009)+(15.047), (I-052)+(5.009)+(15.063), (I-052)+(5.009)+(15.064), (I-052)+(5.011)+(9.002), (I-052)+(5.011)+(15.012), (I-052)+(5.011)+(15.016), (I-052)+(5.011)+(15.025), (I-052)+(5.011)+(15.027), (I-052)+(5.011)+(15.047), (I-052)+(5.011)+(15.063), (I-052)+(5.011)+(15.064), (I-052)+(5.012)+(9.002), (I-052)+(5.012)+(15.012), (I-052)+(5.012)+(15.016), (I-052)+(5.012)+(15.025), (I-052)+(5.012)+(15.027), (I-052)+(5.012)+(15.047), (I-052)+(5.012)+(15.063), (I-052)+(5.012)+(15.064), (I-052)+(5.013)+(9.002), (I-052)+(5.013)+(15.012), (I-052)+(5.013)+(15.016), (I-052)+(5.013)+(15.025), (I-052)+(5.013)+(15.027), (I-052)+(5.013)+(15.047), (I-052)+(5.013)+(15.063), (I-052)+(5.013)+(15.064), (I-052)+(5.015)+(9.002), (I-052)+(5.015)+(15.012), (I-052)+(5.015)+(15.016), (I-052)+(5.015)+(15.025), (I-052)+(5.015)+(15.027), (I-052)+(5.015)+(15.047), (I-052)+(5.015)+(15.063), (I-052)+(5.015)+(15.064), (I-052)+(5.018)+(9.002), (I-052)+(5.018)+(15.012), (I-052)+(5.018)+(15.016), (I-052)+(5.018)+(15.025), (I-052)+(5.018)+(15.027), (I-052)+(5.018)+(15.047), (I-052)+(5.018)+(15.063), (I-052)+(5.018)+(15.064), (I-052)+(5.019)+(9.002), (I-052)+(5.019)+(15.012), (I-052)+(5.019)+(15.016), (I-052)+(5.019)+(15.025), (I-052)+(5.019)+(15.027), (I-052)+(5.019)+(15.047), (I-052)+(5.019)+(15.063), (I-052)+(5.019)+(15.064).

If two compounds (B) are present in the combinations according to the invention, more preferred compound combinations are selected from the group (G3-C1) consisting of the following mixtures:

(I-300)+(1.001)+(1.002), (I-300)+(1.001)+(1.003), (I-300)+(1.001)+(1.004), (I-300)+(1.001)+(1.005), (I-300)+(1.001)+(1.006), (I-300)+(1.001)+(1.007), (I-300)+(1.001)+(1.010), (I-300)+(1.001)+(1.011), (I-300)+(1.001)+(1.012), (I-300)+(1.001)+(1.013), (I-300)+(1.001)+(1.017), (I-300)+(1.001)+(1.018), (I-300)+(1.001)+(1.020), (I-300)+(1.001)+(1.021), (I-300)+(1.001)+(1.026), (I-300)+(1.001)+(1.027), (I-300)+(1.001)+(1.055), (I-300)+(1.001)+(1.059), (I-300)+(1.001)+(1.092), (I-300)+(1.001)+(2.001), (I-300)+(1.001)+(2.002), (I-300)+(1.001)+(2.003), (I-300)+(1.001)+(2.005), (I-300)+(1.001)+(2.007), (I-300)+(1.001)+(2.009), (I-300)+(1.001)+(2.010), (I-300)+(1.001)+(2.011), (I-300)+(1.001)+(2.012), (I-300)+(1.001)+(2.013), (I-300)+(1.001)+(2.014), (I-300)+(1.001)+(2.015), (I-300)+(1.001)+(2.016), (I-300)+(1.001)+(2.017), (I-300)+(1.001)+(2.018), (I-300)+(1.001)+(2.019), (I-300)+(1.001)+(2.021), (I-300)+(1.001)+(2.028), (I-300)+(1.001)+(2.030), (I-300)+(1.001)+(2.038), (I-300)+(1.001)+(3.003), (I-300)+(1.001)+(3.007), (I-300)+(1.001)+(3.012), (I-300)+(1.001)+(3.013), (I-300)+(1.001)+(3.016), (I-300)+(1.001)+(3.017), (I-300)+(1.001)+(3.020), (I-300)+(1.001)+(3.025), (I-300)+(1.001)+(3.026), (I-300)+(1.001)+(3.030), (I-300)+(1.001)+(3.031), (I-300)+(1.001)+(5.003), (I-300)+(1.001)+(5.004), (I-300)+(1.001)+(5.005), (I-300)+(1.001)+(5.008), (I-300)+(1.001)+(5.009), (I-300)+(1.001)+(5.011), (I-300)+(1.001)+(5.012), (I-300)+(1.001)+(5.013), (I-300)+(1.001)+(5.015), (I-300)+(1.001)+(5.018), (I-300)+(1.001)+(5.019), (I-300)+(1.001)+(6.002), (I-300)+(1.001)+(7.001), (I-300)+(1.001)+(7.005), (I-300)+(1.001)+(9.002), (I-300)+(1.001)+(9.004), (I-300)+(1.001)+(14.001), (I-300)+(1.001)+(14.002), (I-300)+(1.001)+(15.008), (I-300)+(1.001)+(15.011), (I-300)+(1.001)+(15.012), (I-300)+(1.001)+(15.016), (I-300)+(1.001)+(15.025), (I-300)+(1.001)+(15.027), (I-300)+(1.001)+(15.047), (I-300)+(1.001)+(15.063), (I-300)+(1.001)+(15.064), (I-300)+(1.001)+(16.001), (I-300)+(1.001)+(16.005), 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(I-300)+(3.017)+(5.013), (I-300)+(3.017)+(5.015), (I-300)+(3.017)+(5.018), (I-300)+(3.017)+(5.019), (I-300)+(3.017)+(6.002), (I-300)+(3.017)+(7.001), (I-300)+(3.017)+(7.005), (I-300)+(3.017)+(9.002), (I-300)+(3.017)+(9.004), (I-300)+(3.017)+(14.001), (I-300)+(3.017)+(14.002), (I-300)+(3.017)+(15.008), (I-300)+(3.017)+(15.011), (I-300)+(3.017)+(15.012), (I-300)+(3.017)+(15.016), (I-300)+(3.017)+(15.025), (I-300)+(3.017)+(15.027), (I-300)+(3.017)+(15.047), (I-300)+(3.017)+(15.063), (I-300)+(3.017)+(15.064), (I-300)+(3.017)+(16.001), (I-300)+(3.017)+(16.005), (I-300)+(3.017)+(17.001), (I-300)+(3.017)+(17.002), (I-300)+(3.017)+(17.003), (I-300)+(3.017)+(17.008), (I-300)+(3.017)+(18.001), (I-300)+(3.020)+(3.025), (I-300)+(3.020)+(3.030), (I-300)+(3.020)+(3.031), (I-300)+(3.020)+(5.003), (I-300)+(3.020)+(5.004), (I-300)+(3.020)+(5.005), (I-300)+(3.020)+(5.008), (I-300)+(3.020)+(5.009), (I-300)+(3.020)+(5.011), (I-300)+(3.020)+(5.012), (I-300)+(3.020)+(5.013), (I-300)+(3.020)+(5.015), (I-300)+(3.020)+(5.018), (I-300)+(3.020)+(5.019), (I-300)+(3.020)+(6.002), (I-300)+(3.020)+(7.001), (I-300)+(3.020)+(7.005), (I-300)+(3.020)+(9.002), (I-300)+(3.020)+(9.004), (I-300)+(3.020)+(14.001), (I-300)+(3.020)+(14.002), (I-300)+(3.020)+(15.008), (I-300)+(3.020)+(15.011), (I-300)+(3.020)+(15.012), (I-300)+(3.020)+(15.016), (I-300)+(3.020)+(15.025), (I-300)+(3.020)+(15.027), (I-300)+(3.020)+(15.047), (I-300)+(3.020)+(15.063), (I-300)+(3.020)+(15.064), (I-300)+(3.020)+(16.001), (I-300)+(3.020)+(16.005), (I-300)+(3.020)+(17.001), (I-300)+(3.020)+(17.002), (I-300)+(3.020)+(17.003), (I-300)+(3.020)+(17.008), (I-300)+(3.020)+(18.001), (I-300)+(3.025)+(3.030), (I-300)+(3.025)+(3.031), (I-300)+(3.025)+(5.003), (I-300)+(3.025)+(5.004), (I-300)+(3.025)+(5.005), (I-300)+(3.025)+(5.008), (I-300)+(3.025)+(5.009), (I-300)+(3.025)+(5.011), (I-300)+(3.025)+(5.012), (I-300)+(3.025)+(5.013), (I-300)+(3.025)+(5.015), (I-300)+(3.025)+(5.018), (I-300)+(3.025)+(5.019), (I-300)+(3.025)+(6.002), (I-300)+(3.025)+(7.001), (I-300)+(3.025)+(7.005), (I-300)+(3.025)+(9.002), (I-300)+(3.025)+(9.004), (I-300)+(3.025)+(14.001), (I-300)+(3.025)+(14.002), (I-300)+(3.025)+(15.008), (I-300)+(3.025)+(15.011), (I-300)+(3.025)+(15.012), (I-300)+(3.025)+(15.016), (I-300)+(3.025)+(15.025), (I-300)+(3.025)+(15.027), (I-300)+(3.025)+(15.047), (I-300)+(3.025)+(15.063), (I-300)+(3.025)+(15.064), (I-300)+(3.025)+(16.001), (I-300)+(3.025)+(16.005), (I-300)+(3.025)+(17.001), (I-300)+(3.025)+(17.002), (I-300)+(3.025)+(17.003), (I-300)+(3.025)+(17.008), (I-300)+(3.025)+(18.001), (I-300)+(3.026)+(3.025), (I-300)+(3.026)+(3.030), (I-300)+(3.026)+(3.031), (I-300)+(3.026)+(5.003), (I-300)+(3.026)+(5.004), (I-300)+(3.026)+(5.005), (I-300)+(3.026)+(5.008), (I-300)+(3.026)+(5.009), (I-300)+(3.026)+(5.011), (I-300)+(3.026)+(5.012), (I-300)+(3.026)+(5.013), (I-300)+(3.026)+(5.015), (I-300)+(3.026)+(5.018), (I-300)+(3.026)+(5.019), (I-300)+(3.026)+(6.002), (I-300)+(3.026)+(7.001), (I-300)+(3.026)+(7.005), (I-300)+(3.026)+(9.002), (I-300)+(3.026)+(9.004), (I-300)+(3.026)+(14.001), (I-300)+(3.026)+(14.002), (I-300)+(3.026)+(15.008), (I-300)+(3.026)+(15.011), (I-300)+(3.026)+(15.012), (I-300)+(3.026)+(15.016), (I-300)+(3.026)+(15.025), (I-300)+(3.026)+(15.027), (I-300)+(3.026)+(15.047), (I-300)+(3.026)+(15.063), (I-300)+(3.026)+(15.064), (I-300)+(3.026)+(16.001), (I-300)+(3.026)+(16.005), (I-300)+(3.026)+(17.001), (I-300)+(3.026)+(17.002), (I-300)+(3.026)+(17.003), (I-300)+(3.026)+(17.008), (I-300)+(3.026)+(18.001), (I-300)+(3.030)+(3.025), (I-300)+(3.030)+(3.031), (I-300)+(3.030)+(5.003), (I-300)+(3.030)+(5.004), (I-300)+(3.030)+(5.005), (I-300)+(3.030)+(5.008), (I-300)+(3.030)+(5.009), (I-300)+(3.030)+(5.011), (I-300)+(3.030)+(5.012), (I-300)+(3.030)+(5.013), (I-300)+(3.030)+(5.015), (I-300)+(3.030)+(5.018), (I-300)+(3.030)+(5.019), (I-300)+(3.030)+(6.002), (I-300)+(3.030)+(7.001), (I-300)+(3.030)+(7.005), (I-300)+(3.030)+(9.002), (I-300)+(3.030)+(9.004), (I-300)+(3.030)+(14.001), (I-300)+(3.030)+(14.002), (I-300)+(3.030)+(15.008), (I-300)+(3.030)+(15.011), (I-300)+(3.030)+(15.012), (I-300)+(3.030)+(15.016), (I-300)+(3.030)+(15.025), (I-300)+(3.030)+(15.027), (I-300)+(3.030)+(15.047), (I-300)+(3.030)+(15.063), (I-300)+(3.030)+(15.064), (I-300)+(3.030)+(16.001), (I-300)+(3.030)+(16.005), (I-300)+(3.030)+(17.001), (I-300)+(3.030)+(17.002), (I-300)+(3.030)+(17.003), (I-300)+(3.030)+(17.008), (I-300)+(3.030)+(18.001), (I-300)+(3.031)+(3.025), (I-300)+(3.031)+(3.030), (I-300)+(3.031)+(5.003), (I-300)+(3.031)+(5.004), (I-300)+(3.031)+(5.005), (I-300)+(3.031)+(5.008), (I-300)+(3.031)+(5.009), (I-300)+(3.031)+(5.011), (I-300)+(3.031)+(5.012), (I-300)+(3.031)+(5.013), (I-300)+(3.031)+(5.015), (I-300)+(3.031)+(5.018), (I-300)+(3.031)+(5.019), (I-300)+(3.031)+(6.002), (I-300)+(3.031)+(7.001), (I-300)+(3.031)+(7.005), (I-300)+(3.031)+(9.002), (I-300)+(3.031)+(9.004), (I-300)+(3.031)+(14.001), (I-300)+(3.031)+(14.002), (I-300)+(3.031)+(15.008), (I-300)+(3.031)+(15.011), (I-300)+(3.031)+(15.012), (I-300)+(3.031)+(15.016), (I-300)+(3.031)+(15.025), (I-300)+(3.031)+(15.027), (I-300)+(3.031)+(15.047), (I-300)+(3.031)+(15.063), (I-300)+(3.031)+(15.064), (I-300)+(3.031)+(16.001), (I-300)+(3.031)+(16.005), (I-300)+(3.031)+(17.001), (I-300)+(3.031)+(17.002), (I-300)+(3.031)+(17.003), (I-300)+(3.031)+(17.008), (I-300)+(3.031)+(18.001), (I-300)+(5.003)+(9.002), (I-300)+(5.003)+(15.012), (I-300)+(5.003)+(15.016), (I-300)+(5.003)+(15.025), (I-300)+(5.003)+(15.027), (I-300)+(5.003)+(15.047), (I-300)+(5.003)+(15.063), (I-300)+(5.003)+(15.064), (I-300)+(5.004)+(9.002), (I-300)+(5.004)+(15.012), (I-300)+(5.004)+(15.016), (I-300)+(5.004)+(15.025), (I-300)+(5.004)+(15.027), (I-300)+(5.004)+(15.047), (I-300)+(5.004)+(15.063), (I-300)+(5.004)+(15.064), (I-300)+(5.005)+(9.002), (I-300)+(5.005)+(15.012), (I-300)+(5.005)+(15.016), (I-300)+(5.005)+(15.025), (I-300)+(5.005)+(15.027), (I-300)+(5.005)+(15.047), (I-300)+(5.005)+(15.063), (I-300)+(5.005)+(15.064), (I-300)+(5.008)+(9.002), (I-300)+(5.008)+(15.012), (I-300)+(5.008)+(15.016), (I-300)+(5.008)+(15.025), (I-300)+(5.008)+(15.027), (I-300)+(5.008)+(15.047), (I-300)+(5.008)+(15.063), (I-300)+(5.008)+(15.064), (I-300)+(5.009)+(9.002), (I-300)+(5.009)+(15.012), (I-300)+(5.009)+(15.016), (I-300)+(5.009)+(15.025), (I-300)+(5.009)+(15.027), (I-300)+(5.009)+(15.047), (I-300)+(5.009)+(15.063), (I-300)+(5.009)+(15.064), (I-300)+(5.011)+(9.002), (I-300)+(5.011)+(15.012), (I-300)+(5.011)+(15.016), (I-300)+(5.011)+(15.025), (I-300)+(5.011)+(15.027), (I-300)+(5.011)+(15.047), (I-300)+(5.011)+(15.063), (I-300)+(5.011)+(15.064), (I-300)+(5.012)+(9.002), (I-300)+(5.012)+(15.012), (I-300)+(5.012)+(15.016), (I-300)+(5.012)+(15.025), (I-300)+(5.012)+(15.027), (I-300)+(5.012)+(15.047), (I-300)+(5.012)+(15.063), (I-300)+(5.012)+(15.064), (I-300)+(5.013)+(9.002), (I-300)+(5.013)+(15.012), (I-300)+(5.013)+(15.016), (I-300)+(5.013)+(15.025), (I-300)+(5.013)+(15.027), (I-300)+(5.013)+(15.047), (I-300)+(5.013)+(15.063), (I-300)+(5.013)+(15.064), (I-300)+(5.015)+(9.002), (I-300)+(5.015)+(15.012), (I-300)+(5.015)+(15.016), (I-300)+(5.015)+(15.025), (I-300)+(5.015)+(15.027), (I-300)+(5.015)+(15.047), (I-300)+(5.015)+(15.063), (I-300)+(5.015)+(15.064), (I-300)+(5.018)+(9.002), (I-300)+(5.018)+(15.012), (I-300)+(5.018)+(15.016), (I-300)+(5.018)+(15.025), (I-300)+(5.018)+(15.027), (I-300)+(5.018)+(15.047), (I-300)+(5.018)+(15.063), (I-300)+(5.018)+(15.064), (I-300)+(5.019)+(9.002), (I-300)+(5.019)+(15.012), (I-300)+(5.019)+(15.016), (I-300)+(5.019)+(15.025), (I-300)+(5.019)+(15.027), (I-300)+(5.019)+(15.047), (I-300)+(5.019)+(15.063), (I-300)+(5.019)+(15.064).

If two compounds (B) are present in the combinations according to the invention, more preferred compound combinations are selected from the group (G4-C1) consisting of the following mixtures:

(I-302)+(1.001)+(1.002), (I-302)+(1.001)+(1.003), (I-302)+(1.001)+(1.004), (I-302)+(1.001)+(1.005), (I-302)+(1.001)+(1.006), (I-302)+(1.001)+(1.007), (I-302)+(1.001)+(1.010), (I-302)+(1.001)+(1.011), (I-302)+(1.001)+(1.012), (I-302)+(1.001)+(1.013), (I-302)+(1.001)+(1.017), (I-302)+(1.001)+(1.018), (I-302)+(1.001)+(1.020), (I-302)+(1.001)+(1.021), (I-302)+(1.001)+(1.026), (I-302)+(1.001)+(1.027), (I-302)+(1.001)+(1.055), (I-302)+(1.001)+(1.059), (I-302)+(1.001)+(1.092), (I-302)+(1.001)+(2.001), (I-302)+(1.001)+(2.002), (I-302)+(1.001)+(2.003), (I-302)+(1.001)+(2.005), (I-302)+(1.001)+(2.007), (I-302)+(1.001)+(2.009), (I-302)+(1.001)+(2.010), (I-302)+(1.001)+(2.011), (I-302)+(1.001)+(2.012), (I-302)+(1.001)+(2.013), (I-302)+(1.001)+(2.014), (I-302)+(1.001)+(2.015), (I-302)+(1.001)+(2.016), (I-302)+(1.001)+(2.017), (I-302)+(1.001)+(2.018), (I-302)+(1.001)+(2.019), (I-302)+(1.001)+(2.021), (I-302)+(1.001)+(2.028), (I-302)+(1.001)+(2.030), (I-302)+(1.001)+(2.038), (I-302)+(1.001)+(3.003), (I-302)+(1.001)+(3.007), (I-302)+(1.001)+(3.012), (I-302)+(1.001)+(3.013), (I-302)+(1.001)+(3.016), (I-302)+(1.001)+(3.017), (I-302)+(1.001)+(3.020), (I-302)+(1.001)+(3.025), (I-302)+(1.001)+(3.026), (I-302)+(1.001)+(3.030), (I-302)+(1.001)+(3.031), (I-302)+(1.001)+(5.003), (I-302)+(1.001)+(5.004), (I-302)+(1.001)+(5.005), (I-302)+(1.001)+(5.008), (I-302)+(1.001)+(5.009), (I-302)+(1.001)+(5.011), (I-302)+(1.001)+(5.012), (I-302)+(1.001)+(5.013), (I-302)+(1.001)+(5.015), (I-302)+(1.001)+(5.018), (I-302)+(1.001)+(5.019), (I-302)+(1.001)+(6.002), (I-302)+(1.001)+(7.001), (I-302)+(1.001)+(7.005), (I-302)+(1.001)+(9.002), (I-302)+(1.001)+(9.004), (I-302)+(1.001)+(14.001), (I-302)+(1.001)+(14.002), (I-302)+(1.001)+(15.008), (I-302)+(1.001)+(15.011), (I-302)+(1.001)+(15.012), (I-302)+(1.001)+(15.016), (I-302)+(1.001)+(15.025), (I-302)+(1.001)+(15.027), (I-302)+(1.001)+(15.047), (I-302)+(1.001)+(15.063), (I-302)+(1.001)+(15.064), (I-302)+(1.001)+(16.001), (I-302)+(1.001)+(16.005), (I-302)+(1.001)+(17.001), (I-302)+(1.001)+(17.002), (I-302)+(1.001)+(17.003), (I-302)+(1.001)+(17.008), (I-302)+(1.001)+(18.001), (I-302)+(1.002)+(1.001), (I-302)+(1.002)+(1.003), (I-302)+(1.002)+(1.004), (I-302)+(1.002)+(1.005), (I-302)+(1.002)+(1.006), (I-302)+(1.002)+(1.007), (I-302)+(1.002)+(1.010), (I-302)+(1.002)+(1.011), (I-302)+(1.002)+(1.012), (I-302)+(1.002)+(1.013), (I-302)+(1.002)+(1.017), (I-302)+(1.002)+(1.018), (I-302)+(1.002)+(1.020), (I-302)+(1.002)+(1.021), (I-302)+(1.002)+(1.026), (I-302)+(1.002)+(1.027), (I-302)+(1.002)+(1.055), (I-302)+(1.002)+(1.059), (I-302)+(1.002)+(1.092), (I-302)+(1.002)+(2.001), (I-302)+(1.002)+(2.002), (I-302)+(1.002)+(2.003), (I-302)+(1.002)+(2.005), (I-302)+(1.002)+(2.007), (I-302)+(1.002)+(2.009), (I-302)+(1.002)+(2.010), (I-302)+(1.002)+(2.011), (I-302)+(1.002)+(2.012), (I-302)+(1.002)+(2.013), (I-302)+(1.002)+(2.014), (I-302)+(1.002)+(2.015), (I-302)+(1.002)+(2.016), (I-302)+(1.002)+(2.017), (I-302)+(1.002)+(2.018), (I-302)+(1.002)+(2.019), (I-302)+(1.002)+(2.021), (I-302)+(1.002)+(2.028), (I-302)+(1.002)+(2.030), (I-302)+(1.002)+(2.038), (I-302)+(1.002)+(3.003), (I-302)+(1.002)+(3.007), (I-302)+(1.002)+(3.012), (I-302)+(1.002)+(3.013), (I-302)+(1.002)+(3.016), (I-302)+(1.002)+(3.017), (I-302)+(1.002)+(3.020), (I-302)+(1.002)+(3.025), (I-302)+(1.002)+(3.026), (I-302)+(1.002)+(3.030), (I-302)+(1.002)+(3.031), (I-302)+(1.002)+(5.003), (I-302)+(1.002)+(5.004), (I-302)+(1.002)+(5.005), (I-302)+(1.002)+(5.008), (I-302)+(1.002)+(5.009), (I-302)+(1.002)+(5.011), (I-302)+(1.002)+(5.012), (I-302)+(1.002)+(5.013), (I-302)+(1.002)+(5.015), (I-302)+(1.002)+(5.018), (I-302)+(1.002)+(5.019), (I-302)+(1.002)+(6.002), (I-302)+(1.002)+(7.001), (I-302)+(1.002)+(7.005), (I-302)+(1.002)+(9.002), (I-302)+(1.002)+(9.004), (I-302)+(1.002)+(14.001), (I-302)+(1.002)+(14.002), (I-302)+(1.002)+(15.008), (I-302)+(1.002)+(15.011), (I-302)+(1.002)+(15.012), (I-302)+(1.002)+(15.016), (I-302)+(1.002)+(15.025), 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(I-302)+(3.025)+(15.016), (I-302)+(3.025)+(15.025), (I-302)+(3.025)+(15.027), (I-302)+(3.025)+(15.047), (I-302)+(3.025)+(15.063), (I-302)+(3.025)+(15.064), (I-302)+(3.025)+(16.001), (I-302)+(3.025)+(16.005), (I-302)+(3.025)+(17.001), (I-302)+(3.025)+(17.002), (I-302)+(3.025)+(17.003), (I-302)+(3.025)+(17.008), (I-302)+(3.025)+(18.001), (I-302)+(3.026)+(3.025), (I-302)+(3.026)+(3.030), (I-302)+(3.026)+(3.031), (I-302)+(3.026)+(5.003), (I-302)+(3.026)+(5.004), (I-302)+(3.026)+(5.005), (I-302)+(3.026)+(5.008), (I-302)+(3.026)+(5.009), (I-302)+(3.026)+(5.011), (I-302)+(3.026)+(5.012), (I-302)+(3.026)+(5.013), (I-302)+(3.026)+(5.015), (I-302)+(3.026)+(5.018), (I-302)+(3.026)+(5.019), (I-302)+(3.026)+(6.002), (I-302)+(3.026)+(7.001), (I-302)+(3.026)+(7.005), (I-302)+(3.026)+(9.002), (I-302)+(3.026)+(9.004), (I-302)+(3.026)+(14.001), (I-302)+(3.026)+(14.002), (I-302)+(3.026)+(15.008), (I-302)+(3.026)+(15.011), (I-302)+(3.026)+(15.012), (I-302)+(3.026)+(15.016), (I-302)+(3.026)+(15.025), (I-302)+(3.026)+(15.027), (I-302)+(3.026)+(15.047), (I-302)+(3.026)+(15.063), (I-302)+(3.026)+(15.064), (I-302)+(3.026)+(16.001), (I-302)+(3.026)+(16.005), (I-302)+(3.026)+(17.001), (I-302)+(3.026)+(17.002), (I-302)+(3.026)+(17.003), (I-302)+(3.026)+(17.008), (I-302)+(3.026)+(18.001), (I-302)+(3.030)+(3.025), (I-302)+(3.030)+(3.031), (I-302)+(3.030)+(5.003), (I-302)+(3.030)+(5.004), (I-302)+(3.030)+(5.005), (I-302)+(3.030)+(5.008), (I-302)+(3.030)+(5.009), (I-302)+(3.030)+(5.011), (I-302)+(3.030)+(5.012), (I-302)+(3.030)+(5.013), (I-302)+(3.030)+(5.015), (I-302)+(3.030)+(5.018), (I-302)+(3.030)+(5.019), (I-302)+(3.030)+(6.002), (I-302)+(3.030)+(7.001), (I-302)+(3.030)+(7.005), (I-302)+(3.030)+(9.002), (I-302)+(3.030)+(9.004), (I-302)+(3.030)+(14.001), (I-302)+(3.030)+(14.002), (I-302)+(3.030)+(15.008), (I-302)+(3.030)+(15.011), (I-302)+(3.030)+(15.012), (I-302)+(3.030)+(15.016), (I-302)+(3.030)+(15.025), (I-302)+(3.030)+(15.027), (I-302)+(3.030)+(15.047), (I-302)+(3.030)+(15.063), (I-302)+(3.030)+(15.064), (I-302)+(3.030)+(16.001), (I-302)+(3.030)+(16.005), (I-302)+(3.030)+(17.001), (I-302)+(3.030)+(17.002), (I-302)+(3.030)+(17.003), (I-302)+(3.030)+(17.008), (I-302)+(3.030)+(18.001), (I-302)+(3.031)+(3.025), (I-302)+(3.031)+(3.030), (I-302)+(3.031)+(5.003), (I-302)+(3.031)+(5.004), (I-302)+(3.031)+(5.005), (I-302)+(3.031)+(5.008), (I-302)+(3.031)+(5.009), (I-302)+(3.031)+(5.011), (I-302)+(3.031)+(5.012), (I-302)+(3.031)+(5.013), (I-302)+(3.031)+(5.015), (I-302)+(3.031)+(5.018), (I-302)+(3.031)+(5.019), (I-302)+(3.031)+(6.002), (I-302)+(3.031)+(7.001), (I-302)+(3.031)+(7.005), (I-302)+(3.031)+(9.002), (I-302)+(3.031)+(9.004), (I-302)+(3.031)+(14.001), (I-302)+(3.031)+(14.002), (I-302)+(3.031)+(15.008), (I-302)+(3.031)+(15.011), (I-302)+(3.031)+(15.012), (I-302)+(3.031)+(15.016), (I-302)+(3.031)+(15.025), (I-302)+(3.031)+(15.027), (I-302)+(3.031)+(15.047), (I-302)+(3.031)+(15.063), (I-302)+(3.031)+(15.064), (I-302)+(3.031)+(16.001), (I-302)+(3.031)+(16.005), (I-302)+(3.031)+(17.001), (I-302)+(3.031)+(17.002), (I-302)+(3.031)+(17.003), (I-302)+(3.031)+(17.008), (I-302)+(3.031)+(18.001), (I-302)+(5.003)+(9.002), (I-302)+(5.003)+(15.012), (I-302)+(5.003)+(15.016), (I-302)+(5.003)+(15.025), (I-302)+(5.003)+(15.027), (I-302)+(5.003)+(15.047), (I-302)+(5.003)+(15.063), (I-302)+(5.003)+(15.064), (I-302)+(5.004)+(9.002), (I-302)+(5.004)+(15.012), (I-302)+(5.004)+(15.016), (I-302)+(5.004)+(15.025), (I-302)+(5.004)+(15.027), (I-302)+(5.004)+(15.047), (I-302)+(5.004)+(15.063), (I-302)+(5.004)+(15.064), (I-302)+(5.005)+(9.002), (I-302)+(5.005)+(15.012), (I-302)+(5.005)+(15.016), (I-302)+(5.005)+(15.025), (I-302)+(5.005)+(15.027), (I-302)+(5.005)+(15.047), (I-302)+(5.005)+(15.063), (I-302)+(5.005)+(15.064), (I-302)+(5.008)+(9.002), (I-302)+(5.008)+(15.012), (I-302)+(5.008)+(15.016), (I-302)+(5.008)+(15.025), (I-302)+(5.008)+(15.027), (I-302)+(5.008)+(15.047), (I-302)+(5.008)+(15.063), (I-302)+(5.008)+(15.064), (I-302)+(5.009)+(9.002), (I-302)+(5.009)+(15.012), (I-302)+(5.009)+(15.016), (I-302)+(5.009)+(15.025), (I-302)+(5.009)+(15.027), (I-302)+(5.009)+(15.047), (I-302)+(5.009)+(15.063), (I-302)+(5.009)+(15.064), (I-302)+(5.011)+(9.002), (I-302)+(5.011)+(15.012), (I-302)+(5.011)+(15.016), (I-302)+(5.011)+(15.025), (I-302)+(5.011)+(15.027), (I-302)+(5.011)+(15.047), (I-302)+(5.011)+(15.063), (I-302)+(5.011)+(15.064), (I-302)+(5.012)+(9.002), (I-302)+(5.012)+(15.012), (I-302)+(5.012)+(15.016), (I-302)+(5.012)+(15.025), (I-302)+(5.012)+(15.027), (I-302)+(5.012)+(15.047), (I-302)+(5.012)+(15.063), (I-302)+(5.012)+(15.064), (I-302)+(5.013)+(9.002), (I-302)+(5.013)+(15.012), (I-302)+(5.013)+(15.016), (I-302)+(5.013)+(15.025), (I-302)+(5.013)+(15.027), (I-302)+(5.013)+(15.047), (I-302)+(5.013)+(15.063), (I-302)+(5.013)+(15.064), (I-302)+(5.015)+(9.002), (I-302)+(5.015)+(15.012), (I-302)+(5.015)+(15.016), (I-302)+(5.015)+(15.025), (I-302)+(5.015)+(15.027), (I-302)+(5.015)+(15.047), (I-302)+(5.015)+(15.063), (I-302)+(5.015)+(15.064), (I-302)+(5.018)+(9.002), (I-302)+(5.018)+(15.012), (I-302)+(5.018)+(15.016), (I-302)+(5.018)+(15.025), (I-302)+(5.018)+(15.027), (I-302)+(5.018)+(15.047), (I-302)+(5.018)+(15.063), (I-302)+(5.018)+(15.064), (I-302)+(5.019)+(9.002), (I-302)+(5.019)+(15.012), (I-302)+(5.019)+(15.016), (I-302)+(5.019)+(15.025), (I-302)+(5.019)+(15.027), (I-302)+(5.019)+(15.047), (I-302)+(5.019)+(15.063), (I-302)+(5.019)+(15.064).

If two compounds (B) are present in the combinations according to the invention, preferred compound combinations are also selected from the group (G6-C) consisting of the following mixtures:

(I-339)+(1.001)+(1.002), (I-339)+(1.001)+(1.003), (I-339)+(1.001)+(1.004), (I-339)+(1.001)+(1.005), (I-339)+(1.001)+(1.006), (I-339)+(1.001)+(1.007), (I-339)+(1.001)+(1.008), (I-339)+(1.001)+(1.009), (I-339)+(1.001)+(1.010), (I-339)+(1.001)+(1.011), (I-339)+(1.001)+(1.012), (I-339)+(1.001)+(1.013), (I-339)+(1.001)+(1.014), (I-339)+(1.001)+(1.015), (I-339)+(1.001)+(1.016), (I-339)+(1.001)+(1.017), (I-339)+(1.001)+(1.018), (I-339)+(1.001)+(1.019), (I-339)+(1.001)+(1.020), (I-339)+(1.001)+(1.021), (I-339)+(1.001)+(1.022), (I-339)+(1.001)+(1.023), (I-339)+(1.001)+(1.024), (I-339)+(1.001)+(1.025), (I-339)+(1.001)+(1.026), (I-339)+(1.001)+(1.027), (I-339)+(1.001)+(1.028), (I-339)+(1.001)+(1.029), (I-339)+(1.001)+(1.030), (I-339)+(1.001)+(1.031), (I-339)+(1.001)+(1.032), (I-339)+(1.001)+(1.033), (I-339)+(1.001)+(1.034), (I-339)+(1.001)+(1.035), (I-339)+(1.001)+(1.036), (I-339)+(1.001)+(1.037), (I-339)+(1.001)+(1.038), (I-339)+(1.001)+(1.039), (I-339)+(1.001)+(1.040), (I-339)+(1.001)+(1.041), (I-339)+(1.001)+(1.042), (I-339)+(1.001)+(1.043), (I-339)+(1.001)+(1.044), (I-339)+(1.001)+(1.045), (I-339)+(1.001)+(1.046), (I-339)+(1.001)+(1.047), (I-339)+(1.001)+(1.048), (I-339)+(1.001)+(1.049), (I-339)+(1.001)+(1.050), (I-339)+(1.001)+(1.051), (I-339)+(1.001)+(1.052), (I-339)+(1.001)+(1.053), (I-339)+(1.001)+(1.054), (I-339)+(1.001)+(1.055), (I-339)+(1.001)+(1.056), (I-339)+(1.001)+(1.057), (I-339)+(1.001)+(1.058), (I-339)+(1.001)+(1.059), (I-339)+(1.001)+(1.060), (I-339)+(1.001)+(1.061), (I-339)+(1.001)+(1.062), (I-339)+(1.001)+(1.063), (I-339)+(1.001)+(1.064), (I-339)+(1.001)+(1.065), (I-339)+(1.001)+(1.066), (I-339)+(1.001)+(1.067), (I-339)+(1.001)+(1.068), (I-339)+(1.001)+(1.069), (I-339)+(1.001)+(1.070), (I-339)+(1.001)+(1.071), (I-339)+(1.001)+(1.072), (I-339)+(1.001)+(1.073), (I-339)+(1.001)+(1.074), (I-339)+(1.001)+(1.075), (I-339)+(1.001)+(1.076), (I-339)+(1.001)+(1.077), (I-339)+(1.001)+(1.078), (I-339)+(1.001)+(1.079), (I-339)+(1.001)+(1.080), (I-339)+(1.001)+(1.081), (I-339)+(1.001)+(1.082), (I-339)+(1.001)+(1.083), (I-339)+(1.001)+(1.084), (I-339)+(1.001)+(1.085), (I-339)+(1.001)+(1.086), (I-339)+(1.001)+(1.087), (I-339)+(1.001)+(1.088), (I-339)+(1.001)+(1.089), (I-339)+(1.001)+(1.090), (I-339)+(1.001)+(1.091), (I-339)+(1.001)+(1.092), (I-339)+(1.001)+(2.001), (I-339)+(1.001)+(2.002), (I-339)+(1.001)+(2.003), (I-339)+(1.001)+(2.004), (I-339)+(1.001)+(2.005), (I-339)+(1.001)+(2.006), (I-339)+(1.001)+(2.007), (I-339)+(1.001)+(2.008), (I-339)+(1.001)+(2.009), (I-339)+(1.001)+(2.010), (I-339)+(1.001)+(2.011), (I-339)+(1.001)+(2.012), (I-339)+(1.001)+(2.013), (I-339)+(1.001)+(2.014), (I-339)+(1.001)+(2.015), (I-339)+(1.001)+(2.016), (I-339)+(1.001)+(2.017), (I-339)+(1.001)+(2.018), (I-339)+(1.001)+(2.019), (I-339)+(1.001)+(2.020), (I-339)+(1.001)+(2.021), (I-339)+(1.001)+(2.022), (I-339)+(1.001)+(2.023), (I-339)+(1.001)+(2.024), (I-339)+(1.001)+(2.025), (I-339)+(1.001)+(2.026), (I-339)+(1.001)+(2.027), (I-339)+(1.001)+(2.028), (I-339)+(1.001)+(2.029), (I-339)+(1.001)+(2.030), (I-339)+(1.001)+(2.031), (I-339)+(1.001)+(2.032), (I-339)+(1.001)+(2.033), (I-339)+(1.001)+(2.034), (I-339)+(1.001)+(2.035), (I-339)+(1.001)+(2.036), (I-339)+(1.001)+(2.037), (I-339)+(1.001)+(2.038), (I-339)+(1.001)+(2.039), (I-339)+(1.001)+(2.040), (I-339)+(1.001)+(2.041), (I-339)+(1.001)+(2.042), (I-339)+(1.001)+(2.043), (I-339)+(1.001)+(2.044), (I-339)+(1.001)+(2.045), (I-339)+(1.001)+(2.046), (I-339)+(1.001)+(2.047), (I-339)+(1.001)+(2.048), (I-339)+(1.001)+(2.049), (I-339)+(1.001)+(2.050), (I-339)+(1.001)+(2.051), (I-339)+(1.001)+(2.052), (I-339)+(1.001)+(2.053), (I-339)+(1.001)+(2.054), (I-339)+(1.001)+(2.055), (I-339)+(1.001)+(2.056), (I-339)+(1.001)+(2.057), (I-339)+(1.001)+(2.058), (I-339)+(1.001)+(2.059), (I-339)+(1.001)+(3.001), (I-339)+(1.001)+(3.002), (I-339)+(1.001)+(3.003), (I-339)+(1.001)+(3.004), (I-339)+(1.001)+(3.005), (I-339)+(1.001)+(3.006), (I-339)+(1.001)+(3.007), (I-339)+(1.001)+(3.008), (I-339)+(1.001)+(3.009), (I-339)+(1.001)+(3.010), (I-339)+(1.001)+(3.011), (I-339)+(1.001)+(3.012), (I-339)+(1.001)+(3.013), (I-339)+(1.001)+(3.014), (I-339)+(1.001)+(3.015), (I-339)+(1.001)+(3.016), (I-339)+(1.001)+(3.017), (I-339)+(1.001)+(3.018), (I-339)+(1.001)+(3.019), (I-339)+(1.001)+(3.020), (I-339)+(1.001)+(3.021), (I-339)+(1.001)+(3.022), (I-339)+(1.001)+(3.023), (I-339)+(1.001)+(3.024), (I-339)+(1.001)+(3.025), (I-339)+(1.001)+(3.026), (I-339)+(1.001)+(3.027), (I-339)+(1.001)+(3.028), (I-339)+(1.001)+(3.029), (I-339)+(1.001)+(3.030), (I-339)+(1.001)+(3.031), (I-339)+(1.001)+(5.001), (I-339)+(1.001)+(5.002), (I-339)+(1.001)+(5.003), (I-339)+(1.001)+(5.004), (I-339)+(1.001)+(5.005), (I-339)+(1.001)+(5.006), (I-339)+(1.001)+(5.007), (I-339)+(1.001)+(5.008), (I-339)+(1.001)+(5.009), (I-339)+(1.001)+(5.010), (I-339)+(1.001)+(5.011), (I-339)+(1.001)+(5.012), (I-339)+(1.001)+(5.013), (I-339)+(1.001)+(5.014), (I-339)+(1.001)+(5.015), (I-339)+(1.001)+(5.016), (I-339)+(1.001)+(5.017), (I-339)+(1.001)+(5.018), (I-339)+(1.001)+(5.019), (I-339)+(1.001)+(5.020), (I-339)+(1.001)+(5.021), (I-339)+(1.001)+(5.022), (I-339)+(1.001)+(5.023), (I-339)+(1.001)+(6.001), (I-339)+(1.001)+(6.002), (I-339)+(1.001)+(6.003), (I-339)+(1.001)+(6.004), (I-339)+(1.001)+(7.001), (I-339)+(1.001)+(7.002), (I-339)+(1.001)+(7.003), (I-339)+(1.001)+(7.004), (I-339)+(1.001)+(7.005), (I-339)+(1.001)+(7.006), (I-339)+(1.001)+(9.001), (I-339)+(1.001)+(9.002), (I-339)+(1.001)+(9.003), (I-339)+(1.001)+(9.004), (I-339)+(1.001)+(9.005), (I-339)+(1.001)+(9.006), (I-339)+(1.001)+(9.007), (I-339)+(1.001)+(9.008), (I-339)+(1.001)+(9.009), (I-339)+(1.001)+(14.001), (I-339)+(1.001)+(14.002), (I-339)+(1.001)+(15.008), (I-339)+(1.001)+(15.011), (I-339)+(1.001)+(15.012), (I-339)+(1.001)+(15.016), (I-339)+(1.001)+(15.025), (I-339)+(1.001)+(15.027), (I-339)+(1.001)+(15.047), (I-339)+(1.001)+(15.063), (I-339)+(1.001)+(15.064), (I-339)+(1.001)+(16.001), (I-339)+(1.001)+(16.002), (I-339)+(1.001)+(16.003), (I-339)+(1.001)+(16.004), (I-339)+(1.001)+(16.005), 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(I-339)+(3.031)+(15.012), (I-339)+(3.031)+(15.016), (I-339)+(3.031)+(15.025), (I-339)+(3.031)+(15.027), (I-339)+(3.031)+(15.047), (I-339)+(3.031)+(15.063), (I-339)+(3.031)+(15.064), (I-339)+(3.031)+(16.001), (I-339)+(3.031)+(16.002), (I-339)+(3.031)+(16.003), (I-339)+(3.031)+(16.004), (I-339)+(3.031)+(16.005), (I-339)+(3.031)+(16.006), (I-339)+(3.031)+(16.007), (I-339)+(3.031)+(16.008), (I-339)+(3.031)+(17.001), (I-339)+(3.031)+(17.002), (I-339)+(3.031)+(17.003), (I-339)+(3.031)+(17.004), (I-339)+(3.031)+(17.005), (I-339)+(3.031)+(17.006), (I-339)+(3.031)+(17.007), (I-339)+(3.031)+(17.008), (I-339)+(3.031)+(17.009), (I-339)+(3.031)+(17.010), (I-339)+(3.031)+(17.011), (I-339)+(3.031)+(17.012), (I-339)+(3.031)+(18.001), (I-339)+(5.001)+(9.001), (I-339)+(5.001)+(9.002), (I-339)+(5.001)+(9.003), (I-339)+(5.001)+(9.004), (I-339)+(5.001)+(9.005), (I-339)+(5.001)+(9.006), (I-339)+(5.001)+(9.007), (I-339)+(5.001)+(9.008), (I-339)+(5.001)+(9.009), (I-339)+(5.001)+(15.012), (I-339)+(5.001)+(15.016), (I-339)+(5.001)+(15.025), (I-339)+(5.001)+(15.027), (I-339)+(5.001)+(15.047), (I-339)+(5.001)+(15.063), (I-339)+(5.001)+(15.064), (I-339)+(5.002)+(9.001), (I-339)+(5.002)+(9.002), (I-339)+(5.002)+(9.003), (I-339)+(5.002)+(9.004), (I-339)+(5.002)+(9.005), (I-339)+(5.002)+(9.006), (I-339)+(5.002)+(9.007), (I-339)+(5.002)+(9.008), (I-339)+(5.002)+(9.009), (I-339)+(5.002)+(15.012), (I-339)+(5.002)+(15.016), (I-339)+(5.002)+(15.025), (I-339)+(5.002)+(15.027), (I-339)+(5.002)+(15.047), (I-339)+(5.002)+(15.063), (I-339)+(5.002)+(15.064), (I-339)+(5.003)+(9.001), (I-339)+(5.003)+(9.002), (I-339)+(5.003)+(9.003), (I-339)+(5.003)+(9.004), (I-339)+(5.003)+(9.005), (I-339)+(5.003)+(9.006), (I-339)+(5.003)+(9.007), (I-339)+(5.003)+(9.008), (I-339)+(5.003)+(9.009), (I-339)+(5.003)+(15.012), (I-339)+(5.003)+(15.016), (I-339)+(5.003)+(15.025), (I-339)+(5.003)+(15.027), (I-339)+(5.003)+(15.047), (I-339)+(5.003)+(15.063), (I-339)+(5.003)+(15.064), (I-339)+(5.004)+(9.001), (I-339)+(5.004)+(9.002), (I-339)+(5.004)+(9.003), (I-339)+(5.004)+(9.004), (I-339)+(5.004)+(9.005), (I-339)+(5.004)+(9.006), (I-339)+(5.004)+(9.007), (I-339)+(5.004)+(9.008), (I-339)+(5.004)+(9.009), (I-339)+(5.004)+(15.012), (I-339)+(5.004)+(15.016), (I-339)+(5.004)+(15.025), (I-339)+(5.004)+(15.027), (I-339)+(5.004)+(15.047), (I-339)+(5.004)+(15.063), (I-339)+(5.004)+(15.064), (I-339)+(5.005)+(9.001), (I-339)+(5.005)+(9.002), (I-339)+(5.005)+(9.003), (I-339)+(5.005)+(9.004), (I-339)+(5.005)+(9.005), (I-339)+(5.005)+(9.006), (I-339)+(5.005)+(9.007), (I-339)+(5.005)+(9.008), (I-339)+(5.005)+(9.009), (I-339)+(5.005)+(15.012), (I-339)+(5.005)+(15.016), (I-339)+(5.005)+(15.025), (I-339)+(5.005)+(15.027), (I-339)+(5.005)+(15.047), (I-339)+(5.005)+(15.063), (I-339)+(5.005)+(15.064), (I-339)+(5.006)+(9.001), (I-339)+(5.006)+(9.002), (I-339)+(5.006)+(9.003), (I-339)+(5.006)+(9.004), (I-339)+(5.006)+(9.005), (I-339)+(5.006)+(9.006), (I-339)+(5.006)+(9.007), (I-339)+(5.006)+(9.008), (I-339)+(5.006)+(9.009), (I-339)+(5.006)+(15.012), (I-339)+(5.006)+(15.016), (I-339)+(5.006)+(15.025), (I-339)+(5.006)+(15.027), (I-339)+(5.006)+(15.047), (I-339)+(5.006)+(15.063), (I-339)+(5.006)+(15.064), (I-339)+(5.007)+(9.001), (I-339)+(5.007)+(9.002), (I-339)+(5.007)+(9.003), (I-339)+(5.007)+(9.004), (I-339)+(5.007)+(9.005), (I-339)+(5.007)+(9.006), (I-339)+(5.007)+(9.007), (I-339)+(5.007)+(9.008), (I-339)+(5.007)+(9.009), (I-339)+(5.007)+(15.012), (I-339)+(5.007)+(15.016), (I-339)+(5.007)+(15.025), (I-339)+(5.007)+(15.027), (I-339)+(5.007)+(15.047), (I-339)+(5.007)+(15.063), (I-339)+(5.007)+(15.064), (I-339)+(5.008)+(9.001), (I-339)+(5.008)+(9.002), (I-339)+(5.008)+(9.003), (I-339)+(5.008)+(9.004), (I-339)+(5.008)+(9.005), (I-339)+(5.008)+(9.006), (I-339)+(5.008)+(9.007), (I-339)+(5.008)+(9.008), (I-339)+(5.008)+(9.009), (I-339)+(5.008)+(15.012), (I-339)+(5.008)+(15.016), (I-339)+(5.008)+(15.025), (I-339)+(5.008)+(15.027), (I-339)+(5.008)+(15.047), (I-339)+(5.008)+(15.063), (I-339)+(5.008)+(15.064), (I-339)+(5.009)+(9.001), (I-339)+(5.009)+(9.002), (I-339)+(5.009)+(9.003), (I-339)+(5.009)+(9.004), (I-339)+(5.009)+(9.005), (I-339)+(5.009)+(9.006), (I-339)+(5.009)+(9.007), (I-339)+(5.009)+(9.008), (I-339)+(5.009)+(9.009), (I-339)+(5.009)+(15.012), (I-339)+(5.009)+(15.016), (I-339)+(5.009)+(15.025), (I-339)+(5.009)+(15.027), (I-339)+(5.009)+(15.047), (I-339)+(5.009)+(15.063), (I-339)+(5.009)+(15.064), (I-339)+(5.010)+(9.001), (I-339)+(5.010)+(9.002), (I-339)+(5.010)+(9.003), (I-339)+(5.010)+(9.004), (I-339)+(5.010)+(9.005), (I-339)+(5.010)+(9.006), (I-339)+(5.010)+(9.007), (I-339)+(5.010)+(9.008), (I-339)+(5.010)+(9.009), (I-339)+(5.010)+(15.012), (I-339)+(5.010)+(15.016), (I-339)+(5.010)+(15.025), (I-339)+(5.010)+(15.027), (I-339)+(5.010)+(15.047), (I-339)+(5.010)+(15.063), (I-339)+(5.010)+(15.064), (I-339)+(5.011)+(9.001), (I-339)+(5.011)+(9.002), (I-339)+(5.011)+(9.003), (I-339)+(5.011)+(9.004), (I-339)+(5.011)+(9.005), (I-339)+(5.011)+(9.006), (I-339)+(5.011)+(9.007), (I-339)+(5.011)+(9.008), (I-339)+(5.011)+(9.009), (I-339)+(5.011)+(15.012), (I-339)+(5.011)+(15.016), (I-339)+(5.011)+(15.025), (I-339)+(5.011)+(15.027), (I-339)+(5.011)+(15.047), (I-339)+(5.011)+(15.063), (I-339)+(5.011)+(15.064), (I-339)+(5.012)+(9.001), (I-339)+(5.012)+(9.002), (I-339)+(5.012)+(9.003), (I-339)+(5.012)+(9.004), (I-339)+(5.012)+(9.005), (I-339)+(5.012)+(9.006), (I-339)+(5.012)+(9.007), (I-339)+(5.012)+(9.008), (I-339)+(5.012)+(9.009), (I-339)+(5.012)+(15.012), (I-339)+(5.012)+(15.016), (I-339)+(5.012)+(15.025), (I-339)+(5.012)+(15.027), (I-339)+(5.012)+(15.047), (I-339)+(5.012)+(15.063), (I-339)+(5.012)+(15.064), (I-339)+(5.013)+(9.001), (I-339)+(5.013)+(9.002), (I-339)+(5.013)+(9.003), (I-339)+(5.013)+(9.004), (I-339)+(5.013)+(9.005), (I-339)+(5.013)+(9.006), (I-339)+(5.013)+(9.007), (I-339)+(5.013)+(9.008), (I-339)+(5.013)+(9.009), (I-339)+(5.013)+(15.012), (I-339)+(5.013)+(15.016), (I-339)+(5.013)+(15.025), (I-339)+(5.013)+(15.027), (I-339)+(5.013)+(15.047), (I-339)+(5.013)+(15.063), (I-339)+(5.013)+(15.064), (I-339)+(5.014)+(9.001), (I-339)+(5.014)+(9.002), (I-339)+(5.014)+(9.003), (I-339)+(5.014)+(9.004), (I-339)+(5.014)+(9.005), (I-339)+(5.014)+(9.006), (I-339)+(5.014)+(9.007), (I-339)+(5.014)+(9.008), (I-339)+(5.014)+(9.009), (I-339)+(5.014)+(15.012), (I-339)+(5.014)+(15.016), (I-339)+(5.014)+(15.025), (I-339)+(5.014)+(15.027), (I-339)+(5.014)+(15.047), (I-339)+(5.014)+(15.063), (I-339)+(5.014)+(15.064), (I-339)+(5.015)+(9.001), (I-339)+(5.015)+(9.002), (I-339)+(5.015)+(9.003), (I-339)+(5.015)+(9.004), (I-339)+(5.015)+(9.005), (I-339)+(5.015)+(9.006), (I-339)+(5.015)+(9.007), (I-339)+(5.015)+(9.008), (I-339)+(5.015)+(9.009), (I-339)+(5.015)+(15.012), (I-339)+(5.015)+(15.016), (I-339)+(5.015)+(15.025), (I-339)+(5.015)+(15.027), (I-339)+(5.015)+(15.047), (I-339)+(5.015)+(15.063), (I-339)+(5.015)+(15.064), (I-339)+(5.016)+(9.001), (I-339)+(5.016)+(9.002), (I-339)+(5.016)+(9.003), (I-339)+(5.016)+(9.004), (I-339)+(5.016)+(9.005), (I-339)+(5.016)+(9.006), (I-339)+(5.016)+(9.007), (I-339)+(5.016)+(9.008), (I-339)+(5.016)+(9.009), (I-339)+(5.016)+(15.012), (I-339)+(5.016)+(15.016), (I-339)+(5.016)+(15.025), (I-339)+(5.016)+(15.027), (I-339)+(5.016)+(15.047), (I-339)+(5.016)+(15.063), (I-339)+(5.016)+(15.064), (I-339)+(5.017)+(9.001), (I-339)+(5.017)+(9.002), (I-339)+(5.017)+(9.003), (I-339)+(5.017)+(9.004), (I-339)+(5.017)+(9.005), (I-339)+(5.017)+(9.006), (I-339)+(5.017)+(9.007), (I-339)+(5.017)+(9.008), (I-339)+(5.017)+(9.009), (I-339)+(5.017)+(15.012), (I-339)+(5.017)+(15.016), (I-339)+(5.017)+(15.025), (I-339)+(5.017)+(15.027), (I-339)+(5.017)+(15.047), (I-339)+(5.017)+(15.063), (I-339)+(5.017)+(15.064), (I-339)+(5.018)+(9.001), (I-339)+(5.018)+(9.002), (I-339)+(5.018)+(9.003), (I-339)+(5.018)+(9.004), (I-339)+(5.018)+(9.005), (I-339)+(5.018)+(9.006), (I-339)+(5.018)+(9.007), (I-339)+(5.018)+(9.008), (I-339)+(5.018)+(9.009), (I-339)+(5.018)+(15.012), (I-339)+(5.018)+(15.016), (I-339)+(5.018)+(15.025), (I-339)+(5.018)+(15.027), (I-339)+(5.018)+(15.047), (I-339)+(5.018)+(15.063), (I-339)+(5.018)+(15.064), (I-339)+(5.019)+(9.001), (I-339)+(5.019)+(9.002), (I-339)+(5.019)+(9.003), (I-339)+(5.019)+(9.004), (I-339)+(5.019)+(9.005), (I-339)+(5.019)+(9.006), (I-339)+(5.019)+(9.007), (I-339)+(5.019)+(9.008), (I-339)+(5.019)+(9.009), (I-339)+(5.019)+(15.012), (I-339)+(5.019)+(15.016), (I-339)+(5.019)+(15.025), (I-339)+(5.019)+(15.027), (I-339)+(5.019)+(15.047), (I-339)+(5.019)+(15.063), (I-339)+(5.019)+(15.064), (I-339)+(5.020)+(9.001), (I-339)+(5.020)+(9.002), (I-339)+(5.020)+(9.003), (I-339)+(5.020)+(9.004), (I-339)+(5.020)+(9.005), (I-339)+(5.020)+(9.006), (I-339)+(5.020)+(9.007), (I-339)+(5.020)+(9.008), (I-339)+(5.020)+(9.009), (I-339)+(5.020)+(15.012), (I-339)+(5.020)+(15.016), (I-339)+(5.020)+(15.025), (I-339)+(5.020)+(15.027), (I-339)+(5.020)+(15.047), (I-339)+(5.020)+(15.063), (I-339)+(5.020)+(15.064), (I-339)+(5.021)+(9.001), (I-339)+(5.021)+(9.002), (I-339)+(5.021)+(9.003), (I-339)+(5.021)+(9.004), (I-339)+(5.021)+(9.005), (I-339)+(5.021)+(9.006), (I-339)+(5.021)+(9.007), (I-339)+(5.021)+(9.008), (I-339)+(5.021)+(9.009), (I-339)+(5.021)+(15.012), (I-339)+(5.021)+(15.016), (I-339)+(5.021)+(15.025), (I-339)+(5.021)+(15.027), (I-339)+(5.021)+(15.047), (I-339)+(5.021)+(15.063), (I-339)+(5.021)+(15.064), (I-339)+(5.022)+(9.001), (I-339)+(5.022)+(9.002), (I-339)+(5.022)+(9.003), (I-339)+(5.022)+(9.004), (I-339)+(5.022)+(9.005), (I-339)+(5.022)+(9.006), (I-339)+(5.022)+(9.007), (I-339)+(5.022)+(9.008), (I-339)+(5.022)+(9.009), (I-339)+(5.022)+(15.012), (I-339)+(5.022)+(15.016), (I-339)+(5.022)+(15.025), (I-339)+(5.022)+(15.027), (I-339)+(5.022)+(15.047), (I-339)+(5.022)+(15.063), (I-339)+(5.022)+(15.064), (I-339)+(5.023)+(9.001), (I-339)+(5.023)+(9.002), (I-339)+(5.023)+(9.003), (I-339)+(5.023)+(9.004), (I-339)+(5.023)+(9.005), (I-339)+(5.023)+(9.006), (I-339)+(5.023)+(9.007), (I-339)+(5.023)+(9.008), (I-339)+(5.023)+(9.009), (I-339)+(5.023)+(15.012), (I-339)+(5.023)+(15.016), (I-339)+(5.023)+(15.025), (I-339)+(5.023)+(15.027), (I-339)+(5.023)+(15.047), (I-339)+(5.023)+(15.063), (I-339)+(5.023)+(15.064).

If two compounds (B) are present in the combinations according to the invention, preferred compound combinations are selected from the group (G7-C) consisting of the following mixtures:

(I-338)+(1.001)+(1.002), (I-338)+(1.001)+(1.003), (I-338)+(1.001)+(1.004), (I-338)+(1.001)+(1.005), (I-338)+(1.001)+(1.006), (I-338)+(1.001)+(1.007), (I-338)+(1.001)+(1.008), (I-338)+(1.001)+(1.009), (I-338)+(1.001)+(1.010), (I-338)+(1.001)+(1.011), (I-338)+(1.001)+(1.012), (I-338)+(1.001)+(1.013), (I-338)+(1.001)+(1.014), (I-338)+(1.001)+(1.015), (I-338)+(1.001)+(1.016), (I-338)+(1.001)+(1.017), (I-338)+(1.001)+(1.018), (I-338)+(1.001)+(1.019), (I-338)+(1.001)+(1.020), (I-338)+(1.001)+(1.021), (I-338)+(1.001)+(1.022), (I-338)+(1.001)+(1.023), (I-338)+(1.001)+(1.024), (I-338)+(1.001)+(1.025), (I-338)+(1.001)+(1.026), (I-338)+(1.001)+(1.027), (I-338)+(1.001)+(1.028), (I-338)+(1.001)+(1.029), (I-338)+(1.001)+(1.030), (I-338)+(1.001)+(1.031), (I-338)+(1.001)+(1.032), (I-338)+(1.001)+(1.033), (I-338)+(1.001)+(1.034), (I-338)+(1.001)+(1.035), (I-338)+(1.001)+(1.036), (I-338)+(1.001)+(1.037), (I-338)+(1.001)+(1.038), (I-338)+(1.001)+(1.039), (I-338)+(1.001)+(1.040), (I-338)+(1.001)+(1.041), 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(I-338)+(5.018)+(15.025), (I-338)+(5.018)+(15.027), (I-338)+(5.018)+(15.047), (I-338)+(5.018)+(15.063), (I-338)+(5.018)+(15.064), (I-338)+(5.019)+(9.001), (I-338)+(5.019)+(9.002), (I-338)+(5.019)+(9.003), (I-338)+(5.019)+(9.004), (I-338)+(5.019)+(9.005), (I-338)+(5.019)+(9.006), (I-338)+(5.019)+(9.007), (I-338)+(5.019)+(9.008), (I-338)+(5.019)+(9.009), (I-338)+(5.019)+(15.012), (I-338)+(5.019)+(15.016), (I-338)+(5.019)+(15.025), (I-338)+(5.019)+(15.027), (I-338)+(5.019)+(15.047), (I-338)+(5.019)+(15.063), (I-338)+(5.019)+(15.064), (I-338)+(5.020)+(9.001), (I-338)+(5.020)+(9.002), (I-338)+(5.020)+(9.003), (I-338)+(5.020)+(9.004), (I-338)+(5.020)+(9.005), (I-338)+(5.020)+(9.006), (I-338)+(5.020)+(9.007), (I-338)+(5.020)+(9.008), (I-338)+(5.020)+(9.009), (I-338)+(5.020)+(15.012), (I-338)+(5.020)+(15.016), (I-338)+(5.020)+(15.025), (I-338)+(5.020)+(15.027), (I-338)+(5.020)+(15.047), (I-338)+(5.020)+(15.063), (I-338)+(5.020)+(15.064), (I-338)+(5.021)+(9.001), (I-338)+(5.021)+(9.002), (I-338)+(5.021)+(9.003), (I-338)+(5.021)+(9.004), (I-338)+(5.021)+(9.005), (I-338)+(5.021)+(9.006), (I-338)+(5.021)+(9.007), (I-338)+(5.021)+(9.008), (I-338)+(5.021)+(9.009), (I-338)+(5.021)+(15.012), (I-338)+(5.021)+(15.016), (I-338)+(5.021)+(15.025), (I-338)+(5.021)+(15.027), (I-338)+(5.021)+(15.047), (I-338)+(5.021)+(15.063), (I-338)+(5.021)+(15.064), (I-338)+(5.022)+(9.001), (I-338)+(5.022)+(9.002), (I-338)+(5.022)+(9.003), (I-338)+(5.022)+(9.004), (I-338)+(5.022)+(9.005), (I-338)+(5.022)+(9.006), (I-338)+(5.022)+(9.007), (I-338)+(5.022)+(9.008), (I-338)+(5.022)+(9.009), (I-338)+(5.022)+(15.012), (I-338)+(5.022)+(15.016), (I-338)+(5.022)+(15.025), (I-338)+(5.022)+(15.027), (I-338)+(5.022)+(15.047), (I-338)+(5.022)+(15.063), (I-338)+(5.022)+(15.064), (I-338)+(5.023)+(9.001), (I-338)+(5.023)+(9.002), (I-338)+(5.023)+(9.003), (I-338)+(5.023)+(9.004), (I-338)+(5.023)+(9.005), (I-338)+(5.023)+(9.006), (I-338)+(5.023)+(9.007), (I-338)+(5.023)+(9.008), (I-338)+(5.023)+(9.009), (I-338)+(5.023)+(15.012), (I-338)+(5.023)+(15.016), (I-338)+(5.023)+(15.025), (I-338)+(5.023)+(15.027), (I-338)+(5.023)+(15.047), (I-338)+(5.023)+(15.063), (I-338)+(5.023)+(15.064).

According to the invention, the expression “combination” stands for the various combinations of compounds (A) and (B), for example in a single “ready-mix” form, in a combined spray mixture composed from separate formulations of the single active compounds, such as a “tank-mix”, and in a combined use of the single active ingredients when applied in a sequential manner, i.e. one after the other within a reasonably short period, such as a few hours or days. Preferably the order of applying the compounds (A) and (B) is not essential for working the present invention.

In the combinations according to the invention the compounds (A) and (B) can be present in a broad range of effective weight ratio of A:B, for example in a range of 250000:1 to 1:250000, preferably in a weight ratio of 5000:1 to 1:5000, more preferably in a weight ratio of 1000:1 to 1:1000, even more preferably in a weight ratio of 500:1 to 1:500, and most preferably in a weight ratio of 100:1 to 1:100.

Further ratios of A:B which can be used according to the present invention are: 95:1 to 1:95, 90:1 to 1:90, 85:1 to 1:85, 80:1 to 1:80, 75:1 to 1:75, 70:1 to 1:70, 65:1 to 1:65, 60:1 to 1:60, 55:1 to 1:55, 50:1 to 1:50, 45:1 to 1:45, 40:1 to 1:40, 35:1 to 1:35, 30:1 to 1:30, 25:1 to 1:25, 20:1 to 1:20, 15:1 to 1:15, 10:1 to 1:10, 5:1 to 1:5, 4:1 to 1:4, 3:1 to 1:3, 2:1 to 1:2.

Further ratios of A:B which can be used according to the present invention are: 1000:1 to 1:1, 500:1 to 1:1, 250:1 to 1:1, 100:1 to 1:1, 95:1 to 1:1, 90:1 to 1:1, 85:1 to 1:1, 80:1 to 1:1, 75:1 to 1:1, 70:1 to 1:1, 65:1 to 1:1, 60:1 to 1:1, 55:1 to 1:1, 50:1 to 1:1, 45:1 to 1:1, 40:1 to 1:1, 35:1 to 1:1, 30:1 to 1:1, 25:1 to 1:1, 20:1 to 1:1, 15:1 to 1:1, 10:1 to 1:1, 5:1 to 1:1, 4:1 to 1:1, 3:1 to 1:1, 2:1 to 1:1.

Further ratios of A:B which can be used according to the present invention are: 1:1 to 1:1000, 1:1 to 1:500, 1:1 to 1:250, 1:1 to 1:100, 1:1 to 1:95, 1:1 to 1:90, 1:1 to 1:85, 1:1 to 1:80, 1:1 to 1:75, 1:1 to 1:70, 1:1 to 1:65, 1:1 to 1:60, 1:1 to 1:55, 1:1 to 1:50, 1:1 to 1:45, 1:1 to 1:40, 1:1 to 1:35, 1:1 to 1:30, 1:1 to 1:25, 1:1 to 1:20, 1:1 to 1:15, 1:1 to 1:10, 1:1 to 1:5, 1:1 to 1:4, 1:1 to 1:3, 1:1 to 1:2.

If more than one, e.g. 2 or 3, compounds (B) are present, the weight ratio refers to the total amount of compound (B), i.e. to the sum of the amount of each compound (B) present in the combination. This applies mutatis mutandis if more than one, e.g. 2 or 3, compounds (A) are present.

If more than one, e.g. 2 or 3, compounds (B) are present in the combinations according to the invention the individual compounds (B) can be present in a broad range of effective weight ratio. If for example 2 compounds (B) are present, which are in the following referred to as compounds (B1) and (B2) the effective weight ratio of B1:B2, can vary for example in a range of 100:1 to 1:100, preferably in a weight ratio of 50:1 to 1:50, most preferably in a weight ratio of 20:1 to 1:20. Further ratios of B1:B2 which can be used according to the present invention with increasing preference in the order given are: 95:1 to 1:95, 90:1 to 1:90, 85:1 to 1:85, 80:1 to 1:80, 75:1 to 1:75, 70:1 to 1:70, 65:1 to 1:65, 60:1 to 1:60, 55:1 to 1:55, 50:1 to 1:50, 45:1 to 1:45, 40:1 to 1:40, 35:1 to 1:35, 30:1 to 1:30, 25:1 to 1:25, 15:1 to 1:15, 10:1 to 1:10, 5:1 to 1:5, 4:1 to 1:4, 3:1 to 1:3, 2:1 to 1:2.

Further ratios of B1:B2 which can be used according to the present invention are: 95:1 to 1:1, 90:1 to 1:1, 85:1 to 1:1, 80:1 to 1:1, 75:1 to 1:1, 70:1 to 1:1, 65:1 to 1:1, 60:1 to 1:1, 55:1 to 1:1, 50:1 to 1:1, 45:1 to 1:1, 40:1 to 1:1, 35:1 to 1:1, 30:1 to 1:1, 25:1 to 1:1, 20:1 to 1:1, 15:1 to 1:1, 10:1 to 1:1, 5:1 to 1:1, 4:1 to 1:1, 3:1 to 1:1, 2:1 to 1:1.

Further ratios of B1:B2 which can be used according to the present invention are: 1:1 to 1:95, 1:1 to 1:90, 1:1 to 1:85, 1:1 to 1:80, 1:1 to 1:75, 1:1 to 1:70, 1:1 to 1:65, 1:1 to 1:60, 1:1 to 1:55, 1:1 to 1:50, 1:1 to 1:45, 1:1 to 1:40, 1:1 to 1:35, 1:1 to 1:30, 1:1 to 1:25, 1:1 to 1:20, 1:1 to 1:15, 1:1 to 1:10, 1:1 to 1:5, 1:1 to 1:4, 1:1 to 1:3, 1:1 to 1:2.

Isomers

Depending on the nature of the substituents of compound (A) and the nature of compound (B), those compounds may be present in the compound combinations of the invention in the form of different stereoisomers. These stereoisomers are, for example, enantiomers, diastereomers, atropisomers or geometric isomers. Accordingly, the invention encompasses both pure stereoisomers and any mixture of these isomers. Where a compound can be present in two or more tautomer forms in equilibrium, reference to the compound by means of one tautomeric description is to be considered to include all tautomer forms. Where a compound can be present in isomeric forms and/or tautomeric forms, such a compound is understood hereinabove and hereinbelow also to include, where applicable, corresponding isomeric and/or tautomeric forms or mixtures thereof, even when these are not specifically mentioned in each case.

Salts/N-Oxides

The compounds present in the compound combination of the invention may independently of one another be present in the form of the free compound and/or, if applicable, an agrochemically active salt and/or a N-oxide thereof.

Agrochemically active salts include acid addition salts of inorganic and organic acids well as salts of customary bases. Examples of inorganic acids are hydrohalic acids, such as hydrogen fluoride, hydrogen chloride, hydrogen bromide and hydrogen iodide, sulfuric acid, phosphoric acid and nitric acid, and acidic salts, such as sodium bisulfate and potassium bisulfate. Useful organic acids include, for example, formic acid, carbonic acid and alkanoic acids such as acetic acid, trifluoroacetic acid, trichloroacetic acid and propionic acid, and also glycolic acid, thiocyanic acid, lactic acid, succinic acid, citric acid, benzoic acid, cinnamic acid, oxalic acid, saturated or mono- or diunsaturated fatty acids having 6 to 20 carbon atoms, alkylsulphuric monoesters, alkylsulphonic acids (sulphonic acids having straight-chain or branched alkyl radicals having 1 to 20 carbon atoms), arylsulphonic acids or aryldisulphonic acids (aromatic radicals, such as phenyl and naphthyl, which bear one or two sulphonic acid groups), alkylphosphonic acids (phosphonic acids having straight-chain or branched alkyl radicals having 1 to 20 carbon atoms), arylphosphonic acids or aryldiphosphonic acids (aromatic radicals, such as phenyl and naphthyl, which bear one or two phosphonic acid radicals), where the alkyl and aryl radicals may bear further substituents, for example p-toluenesulphonic acid, salicylic acid, p-aminosalicylic acid, 2-phenoxybenzoic acid, 2-acetoxybenzoic acid.

N-oxides of compounds present in the compound combination of the invention or intermediates thereof can be obtained in a simple manner by customary processes, for example by N-oxidation with hydrogen peroxide (H₂O₂), peracids, for example peroxy sulfuric acid or peroxy carboxylic acids, such as meta-chloroperoxybenzoic acid or peroxymonosulfuric acid (Caro's acid).

E.g. the corresponding N-oxides may be prepared starting from the respective compounds using conventional oxidation methods, e.g. by treating the compounds with an organic peracid such as metachloroperbenzoic acid (e.g. WO-A 2003/64572 or J. Med. Chem. 38 (11), 1892-1903, 1995); or with inorganic oxidizing agents such as hydrogen peroxide (e.g. J. Heterocyc. Chem. 18 (7), 1305-1308, 1981) or oxone (e.g. J. Am. Chem. Soc. 123 (25), 5962-5973, 2001). The oxidation may lead to pure mono-N-oxides or to a mixture of different N-oxides, which can be separated by conventional methods such as chromatography.

Crystalline Form

The compounds present in the compound combinations of the invention may exist in multiple crystalline and/or amorphous forms. Crystalline forms include unsolvated crystalline forms, solvates and hydrates, in each case of the individual compounds or adducts thereof.

Solvates of the compounds present in the compound combinations of the invention or their salts are stoichiometric compositions of the compounds with solvents.

Formulations

The present invention further relates to compositions for controlling unwanted microorganisms, comprising the compound combination according to the invention. The compositions may be applied to the microorganisms and/or in their habitat.

The composition comprises the compound combination of the invention and at least one agriculturally suitable auxiliary, e.g. carrier(s) and/or surfactant(s).

A carrier is a solid or liquid, natural or synthetic, organic or inorganic substance that is generally inert. The carrier generally improves the application of the compounds, for instance, to plants, plants parts or seeds. Examples of suitable solid carriers include, but are not limited to, ammonium salts, in particular ammonium sulfates, ammonium phosphates and ammonium nitrates, natural rock flours, such as kaolins, clays, talc, chalk, quartz, attapulgite, montmorillonite and diatomaceous earth, silica gel and synthetic rock flours, such as finely divided silica, alumina and silicates. Examples of typically useful solid carriers for preparing granules include, but are not limited to crushed and fractionated natural rocks such as calcite, marble, pumice, sepiolite and dolomite, synthetic granules of inorganic and organic flours and granules of organic material such as paper, sawdust, coconut shells, maize cobs and tobacco stalks. Examples of suitable liquid carriers include, but are not limited to, water, organic solvents and combinations thereof. Examples of suitable solvents include polar and nonpolar organic chemical liquids, for example from the classes of aromatic and nonaromatic hydrocarbons (such as cyclohexane, paraffins, alkylbenzenes, xylene, toluene, tetrahydronaphthalene, alkylnaphthalenes, chlorinated aromatics or chlorinated aliphatic hydrocarbons such as chlorobenzenes, chloroethylenes or methylene chloride), alcohols and polyols (which may optionally also be substituted, etherified and/or esterified, such as ethanol, propanol, butanol, benzylalcohol, cyclohexanol or glycol), ketones (such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone), esters (including fats and oils) and (poly)ethers, unsubstituted and substituted amines, amides (such as dimethylformamide or fatty acid amides) and esters thereof, lactams (such as N-alkylpyrrolidones, in particular N-methylpyrrolidone) and lactones, sulfones and sulfoxides (such as dimethyl sulfoxide), oils of vegetable or animal origin. The carrier may also be a liquefied gaseous extender, i.e. liquid which is gaseous at standard temperature and under standard pressure, for example aerosol propellants such as halohydrocarbons, butane, propane, nitrogen and carbon dioxide.

Preferred solid carriers are selected from clays, talc and silica.

Preferred liquid carriers are selected from water, fatty acid amides and esters thereof, aromatic and nonaromatic hydrocarbons, lactams and carbonic acid esters.

The amount of carrier typically ranges from 1 to 99.99%, preferably from 5 to 99.9%, more preferably from 10 to 99.5%, and most preferably from 20 to 99% by weight of the composition.

Liquid carriers are typically present in a range of from 20 to 90%, for example 30 to 80% by weight of the composition.

Solid carriers are typically present in a range of from 0 to 50%, preferably 5 to 45%, for example 10 to 30% by weight of the composition.

If the composition comprises two or more carriers, the outlined ranges refer to the total amount of carriers.

The surfactant can be an ionic (cationic or anionic), amphoteric or non-ionic surfactant, such as ionic or non-ionic emulsifier(s), foam former(s), dispersant(s), wetting agent(s), penetration enhancer(s) and any mixtures thereof. Examples of suitable surfactants include, but are not limited to, salts of polyacrylic acid, salts of lignosulfonic acid (such as sodium lignosulfonate), salts of phenolsulfonic acid or naphthalenesulfonic acid, polycondensates of ethylene oxide and/or propylene oxide with fatty alcohols, fatty acids or fatty amines (for example, polyoxyethylene fatty acid esters such as castor oil ethoxylate, polyoxyethylene fatty alcohol ethers, for example alkylaryl polyglycol ethers), substituted phenols (preferably alkylphenols or arylphenols) and ethoxylates thereof (such as tristyrylphenol ethoxylate), salts of sulfosuccinic esters, taurine derivatives (preferably alkyl taurates), phosphoric esters of polyethoxylated alcohols or phenols, fatty esters of polyols (such a fatty acid esters of glycerol, sorbitol or sucrose), sulfates (such as alkyl sulfates and alkyl ether sulfates), sulfonates (for example, alkylsulfonates, arylsulfonates and alkylbenzene sulfonates), phosphate esters, protein hydrolysates, lignosulfite waste liquors and methylcellulose. Any reference to salts in this paragraph refers preferably to the respective alkali, alkaline earth and ammonium salts.

Preferred surfactants are selected from polyoxyethylene fatty alcohol ethers, polyoxyethylene fatty acid esters, alkylbenzene sulfonates, such as calcium dodecylbenzenesulfonate, castor oil ethoxylate, sodium lignosulfonate and arylphenol ethoxylates, such as tristyrylphenol ethoxylate.

The amount of surfactants typically ranges from 5 to 40%, for example 10 to 20%, by weight of the composition.

Further examples of suitable auxiliaries include water repellents, siccatives, binders (adhesive, tackifier, fixing agent, such as carboxymethylcellulose, natural and synthetic polymers in the form of powders, granules or latices, such as gum arabic, polyvinyl alcohol and polyvinyl acetate, natural phospholipids such as cephalins and lecithins and synthetic phospholipids, polyvinylpyrrolidone and tylose), thickeners and secondary thickeners (such as cellulose ethers, acrylic acid derivatives, xanthan gum, modified clays, e.g. the products available under the name Bentone, and finely divided silica), stabilizers (e.g. cold stabilizers, preservatives (e.g. dichlorophene and benzyl alcohol hemiformal), antioxidants, light stabilizers, in particular UV stabilizers, or other agents which improve chemical and/or physical stability), dyes or pigments (such as inorganic pigments, e.g. iron oxide, titanium oxide and Prussian Blue; organic dyes, e.g. alizarin, azo and metal phthalocyanine dyes), antifoams (e.g. silicone antifoams and magnesium stearate), antifreezes, stickers, gibberellins and processing auxiliaries, mineral and vegetable oils, perfumes, waxes, nutrients (including trace nutrients, such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc), protective colloids, thixotropic substances, penetrants, sequestering agents and complex formers.

The choice of the auxiliaries depends on the intended mode of application of the compound combination of the invention and/or on the physical properties of the active compound(s) present in said compound combination. Furthermore, the auxiliaries may be chosen to impart particular properties (technical, physical and/or biological properties) to the compositions or use forms prepared therefrom. The choice of auxiliaries may allow customizing the compositions to specific needs.

The composition of the invention may be provided to the end user as ready-for-use formulation, i.e. the compositions may be directly applied to the plants or seeds by a suitable device, such as a spraying or dusting device. Alternatively, the compositions may be provided to the end user in the form of concentrates which have to be diluted, preferably with water, prior to use.

The composition of the invention can be prepared in conventional manners, for example by mixing the compound combination of the invention with one or more suitable auxiliaries, such as disclosed herein above.

The composition comprises a fungicidally effective amount of a compound combination of the invention. The term “effective amount” denotes an amount, which is sufficient for controlling harmful fungi on cultivated plants or in the protection of materials and which does not result in a substantial damage to the treated plants. Such an amount can vary in a broad range and is dependent on various factors, such as the fungal species to be controlled, the treated cultivated plant or material, the climatic conditions and the specific compound combination of the invention used. Usually, the composition according to the invention contains from 0.01 to 99% by weight, preferably from 0.05 to 98% by weight, more preferred from 0.1 to 95% by weight, even more preferably from 0.5 to 90% by weight, most preferably from 1 to 80% by weight of the compound combination of the invention.

The composition of the invention may be in any customary composition type, such as solutions (e.g aqueous solutions), emulsions, water- and oil-based suspensions, powders (e.g. wettable powders, soluble powders), dusts, pastes, granules (e.g. soluble granules, granules for broadcasting), suspoemulsion concentrates, natural or synthetic products impregnated with the compound combination of the invention, fertilizers and also microencapsulations in polymeric substances. The compound combination of the invention may be present in a suspended, emulsified or dissolved form. Examples of particular suitable composition types are solutions, watersoluble concentrates (e.g. SL, LS), dispersible concentrates (DC), suspensions and suspension concentrates (e.g. SC, OD, OF, FS), emulsifiable concentrates (e.g. EC), emulsions (e.g. EW, EO, ES, ME, SE), capsules (e.g. CS, ZC), pastes, pastilles, wettable powders or dusts (e.g. WP, SP, WS, DP, DS), pressings (e.g. BR, TB, DT), granules (e.g. WG, SG, GR, FG, GG, MG), insecticidal articles (e.g. LN), as well as gel formulations for the treatment of plant propagation materials such as seeds (e.g. GW, GF). These and further compositions types are defined by the Food and Agriculture Organization of the United Nations (FAO). An overview is given in the “Catalogue of pesticide formulation types and international coding system”, Technical Monograph No. 2, 6th Ed. May 2008, Croplife International.

Preferably, the composition of the invention is in form of one of the following types: EC, SC, FS, SE, OD and WG, more preferred EC, SC, OD and WG.

Further details about examples of composition types and their preparation are given below. The outlined amount of compound combination of the invention refers to the total amount of compounds (A) and (B) present in the compound combination of the present invention. If two or more representatives of any further component of the composition, e.g. wetting agent, binder, are present, the outlined amounts of the respective component refers to the total amount of all representatives of said component, e.g. all wetting agents, all binders, all solvents and so on.

i) Water-Soluble Concentrates (SL, LS)

10-60% by weight of the compound combination of the invention and 5-15% by weight surfactant (e.g. polyoxyethylene fatty alcohol ether) are dissolved in such amount of water and/or water-soluble solvent (e.g. alcohols such as propylene glycol or carbonates such as propylene carbonate) to result in a total amount of 100% by weight. Before application the concentrate is diluted with water.

ii) Dispersible Concentrates (DC)

5-25% by weight of the compound combination of the invention and 1-10% by weight surfactant and/or binder (e.g. polyvinylpyrrolidone) are dissolved in such amount of organic solvent (e.g. cyclohexanone) to result in a total amount of 100% by weight. Dilution with water gives a dispersion.

iii) Emulsifiable Concentrates (EC)

15-70% by weight of the compound combination of the invention and 5-10% by weight surfactant (e.g. a mixture of calcium dodecylbenzenesulfonate and castor oil ethoxylate) are dissolved in such amount of water-insoluble organic solvent (e.g. aromatic hydrocarbon or fatty acid amide) and if needed additional water-soluble solvent to result in a total amount of 100% by weight. Dilution with water gives an emulsion.

iv) Emulsions (EW, EO, ES)

5-40% by weight of the compound combination of the invention and 1-10% by weight surfactant (e.g. a mixture of calcium dodecylbenzenesulfonate and castor oil ethoxylate) are dissolved in 20-40% by weight water-insoluble organic solvent (e.g. aromatic hydrocarbon). This mixture is added to such amount of water by means of an emulsifying machine to result in a total amount of 100% by weight. The resulting composition is a homogeneous emulsion. Before application the emulsion may be further diluted with water.

v) Suspensions and Suspension Concentrates

v-1) Water-Based (SC, FS)

In a suitable grinding equipment, e.g. an agitated ball mill, 20-60% by weight of the compound combination of the invention are comminuted with addition of 2-10% by weight surfactant (e.g. sodium lignosulfonate and polyoxyethylene fatty alcohol ether), 0.1-2% by weight thickener (e.g. xanthan gum) and water to give a fine active substance suspension. Water is added in such amount to result in a total amount of 100% by weight. Dilution with water gives a stable suspension of the active substances. For FS type compositions up to 40% by weight binder (e.g. polyvinylalcohol) is added.

v-2) Oil-Based (OD, OF)

In a suitable grinding equipment, e.g. an agitated ball mill, 20-60% by weight of the compound combination of the invention are comminuted with addition of 2-10% by weight surfactant (e.g. sodium lignosulfonate and polyoxyethylene fatty alcohol ether), 0.1-2% by weight thickener (e.g. modified clay, in particular Bentone, or silica) and an organic carrier to give a fine active substance oil suspension. The organic carrier is added in such amount to result in a total amount of 100% by weight. Dilution with water gives a stable dispersion of the active substances.

vi) Water-Dispersible Granules and Water-Soluble Granules (WG, SG)

50-80% by weight of the compound combination of the invention are ground finely with addition of surfactant (e.g. sodium lignosulfonate and polyoxyethylene fatty alcohol ether) and converted to water-dispersible or water-soluble granules by means of technical appliances (e. g. extrusion, spray tower, fluidized bed). The surfactant is used in such amount to result in a total amount of 100% by weight. Dilution with water gives a stable dispersion or solution of the active substances.

vii) Water-Dispersible Powders and Water-Soluble Powders (WP, SP, WS)

50-80% by weight of the compound combination of the invention are ground in a suitable mill, preferably a rotor-stator mill, with addition of 1-8% by weight surfactant (e.g. sodium lignosulfonate, polyoxyethylene fatty alcohol ether) and such amount of solid carrier, e.g. silica gel, to result in a total amount of 100% by weight. Dilution with water gives a stable dispersion or solution of the active substances.

viii) Gel (GW, GF)

In a suitable mill, e.g. an agitated ball mill, 5-25% by weight of the compound combination of the invention are comminuted with addition of 3-10% by weight surfactant (e.g. sodium lignosulfonate), 1-5% by weight binder (e.g. carboxymethylcellulose) and such amount of water to result in a total amount of 100% by weight. This results in a fine suspension of the active substance. Dilution with water gives a stable suspension of the active substances.

ix) Microemulsion (ME)

5-20% by weight of the compound combination of the invention are added to 5-30% by weight organic solvent blend (e.g. fatty acid dimethylamide and cyclohexanone), 10-25% by weight surfactant blend (e.g. polyoxyethylene fatty alcohol ether and arylphenol ethoxylate), and such amount of water to result in a total amount of 100% by weight. This mixture is stirred for 1 h to produce spontaneously a thermodynamically stable microemulsion.

x) Microcapsules (CS)

An oil phase comprising 5-50% by weight of the compound combination of the invention, 0-40% by weight water-insoluble organic solvent (e.g. aromatic hydrocarbon), 2-15% by weight acrylic monomers (e.g. methylmethacrylate, methacrylic acid and a di- or triacrylate) are dispersed into an aqueous solution of a protective colloid (e.g. polyvinyl alcohol). Radical polymerization initiated by a radical initiator results in the formation of poly(meth)acrylate microcapsules. Alternatively, an oil phase comprising 5-50% by weight of the compound combination of the invention, 0-40% by weight water-insoluble organic solvent (e.g. aromatic hydrocarbon), and an isocyanate monomer (e.g. diphenylmethene-4,4′-diisocyanatae) are dispersed into an aqueous solution of a protective colloid (e.g. polyvinyl alcohol). The addition of a polyamine (e.g. hexamethylenediamine) results in the formation of polyurea microcapsules. The monomers amount to 1-10% by weight of the total CS composition.

xi) Dustable Powders (DP, DS)

1-10% by weight of the compound combination of the invention are ground finely and mixed intimately with such amount of solid carrier, e.g. finely divided kaolin, to result in a total amount of 100% by weight.

xii) Granules (GR, FG)

0.5-30% by weight of the compound combination of the invention are ground finely and associated with such amount of solid carrier (e.g. silicate) to result in a total amount of 100% by weight. Granulation is achieved by extrusion, spray-drying or the fluidized bed.

xiii) Ultra-Low Volume Liquids (UL)

1-50% by weight of the compound combination of the invention are dissolved in such amount of organic solvent, e.g. aromatic hydrocarbon, to result in a total amount of 100% by weight.

The compositions types i) to xiii) may optionally comprise further auxiliaries, such as 0.1-1% by weight preservatives, 0.1-1% by weight antifoams, 0.1-1% by weight dyes and/or pigments, and 5-10% by weight antifreezes.

Further Active Ingredients

Compound combinations according to the invention can be used as such or in compositions/formulations thereof and can be mixed with further known active ingredients, for example biological control agents, bactericides, acaricides, nematicides or insecticides, in order thus to broaden, for example, the activity spectrum or to prevent development of resistance.

Useful mixing partners include, for example, insecticides, acaricides, nematicides and bactericides (see also Pesticide Manual, 14th ed.).

A mixture with other known active ingredients, such as herbicides, or with fertilizers and growth regulators, safeners and/or semiochemicals, is also possible.

“Insecticides” as well as the term “insecticidal” refers to the ability of a substance to increase mortality or inhibit growth rate of insects. As used herein, the term “insects” comprises all organisms in the class “Insecta”.

“Nematicide” and “nematicidal” refers to the ability of a substance to increase mortality or inhibit the growth rate of nematodes. In general, the term “nematode” comprises eggs, larvae, juvenile and mature forms of said organism.

“Acaricide” and “acaricidal” refers to the ability of a substance to increase mortality or inhibit growth rate of ectoparasites belonging to the class Arachnida, sub-class Acari.

As used herein, the term“biological control” is defined as control of harmful organisms such as a phytopathogenic fungi and/or insects and/or acarids and/or nematodes by the use or employment of a biological control agent.

As used herein, the term “biological control agent” is defined as an organism other than the harmful organisms and/or proteins or secondary metabolites produced by such an organism for the purpose of biological control. Mutants of the second organism shall be included within the definition of the biological control agent. The term “mutant” refers to a variant of the parental strain as well as methods for obtaining a mutant or variant in which the pesticidal activity is greater than that expressed by the parental strain. The “parent strain” is defined herein as the original strain before mutagenesis. To obtain such mutants the parental strain may be treated with a chemical such as N-methyl-N′-nitro-N-nitrosoguanidine, ethylmethanesulfone, or by irradiation using gamma, x-ray, or UV-irradiation, or by other means well known to those skilled in the art. Known mechanisms of biological control agents comprise enteric bacteria that control root rot by out-competing fungi for space on the surface of the root. Bacterial toxins, such as antibiotics, have been used to control pathogens. The toxin can be isolated and applied directly to the plant or the bacterial species may be administered so it produces the toxin in situ.

A “variant” is a strain having all the identifying characteristics of the NRRL or ATCC Accession Numbers as indicated in this text and can be identified as having a genome that hybridizes under conditions of high stringency to the genome of the NRRL or ATCC Accession Numbers.

“Hybridization” refers to a reaction in which one or more polynucleotides react to form a complex that is stabilized via hydrogen bonding between the bases of the nucleotide residues. The hydrogen bonding may occur by Watson-Crick base pairing, Hoogstein binding, or in any other sequence-specific manner. The complex may comprise two strands forming a duplex structure, three or more strands forming a multi-stranded complex, a single self-hybridizing strand, or any combination of these. Hybridization reactions can be performed under conditions of different “stringency”. In general, a low stringency hybridization reaction is carried out at about 40° C. in 10×SSC or a solution of equivalent ionic strength/temperature. A moderate stringency hybridization is typically performed at about 50° C. in 6×SSC, and a high stringency hybridization reaction is generally performed at about 60° C. in 1×SSC.

A variant of the indicated NRRL or ATCC Accession Number may also be defined as a strain having a genomic sequence that is greater than 85%, more preferably greater than 90% or more preferably greater than 95% sequence identity to the genome of the indicated NRRL or ATCC Accession Number. A polynucleotide or polynucleotide region (or a polypeptide or polypeptide region) has a certain percentage (for example, 80%, 85%, 90%, or 95%) of “sequence identity” to another sequence means that, when aligned, that percentage of bases (or amino acids) are the same in comparing the two sequences. This alignment and the percent homology or sequence identity can be determined using software programs known in the art, for example, those described in Current Protocols in Molecular Biology (F. M. Ausubel et al., eds., 1987).

NRRL is the abbreviation for the Agricultural Research Service Culture Collection, an international depositary authority for the purposes of deposing microorganism strains under the Budapest treaty on the international recognition of the deposit of microorganisms for the purposes of patent procedure, having the address National Center for Agricultural Utilization Research, Agricultural Research service, U.S. Department of Agriculture, 1815 North university Street, Peroira, Illinois 61604 USA.

ATCC is the abbreviation for the American Type Culture Collection, an international depositary authority for the purposes of deposing microorganism strains under the Budapest treaty on the international recognition of the deposit of microorganisms for the purposes of patent procedure, having the address ATCC Patent Depository, 10801 University Blvd., Manassas, VA 10110 USA.

Examples of biological control agents which may be combined with the compound combinations of the invention are:

-   -   (A) Antibacterial agents selected from the group of:     -   (A1) bacteria, such as (A1.1) Bacillus subtilis, in particular         strain QST713/AQ713 (available as SERENADE OPTI or SERENADE ASO         from Bayer CropScience LP, US, having NRRL Accession No. B21661         and described in U.S. Pat. No. 6,060,051); (A1.2) Bacillus         amyloliquefaciens, in particular strain D747 (available as         Double Nickel™ from Certis, US, having accession number FERM         BP-8234 and disclosed in U.S. Pat. No. 7,094,592); (A1.3)         Bacillus pumilus, in particular strain BU F-33 (having NRRL         Accession No. 50185); (A1.4) Bacillus subtilis var.         amyloliquefaciens strain FZB24 (available as Taegro® from         Novozymes, US); (A1.5) a Paenibacillus sp. strain having         Accession No. NRRL B-50972 or Accession No. NRRL B-67129 and         described in International Patent Publication No. WO         2016/154297; and     -   (A2) fungi, such as (A2.1) Aureobasidium pullulans, in         particular blastospores of strain DSM14940; (A2.2) Aureobasidium         pullulans blastospores of strain DSM 14941; (A2.3) Aureobasidium         pullulans, in particular mixtures of blastospores of strains         DSM14940 and DSM14941;     -   (B) Biological fungicides selected from the group of:     -   (B1) bacteria, for example (B1.1) Bacillus subtilis, in         particular strain QST713/AQ713 (available as SERENADE OPTI or         SERENADE ASO from Bayer CropScience LP, US, having NRRL         Accession No. B21661 and described in U.S. Pat. No. 6,060,051);         (B1.2) Bacillus pumilus, in particular strain QST2808 (available         as SONATA® from Bayer CropScience LP, US, having Accession No.         NRRL B-30087 and described in U.S. Pat. No. 6,245,551); (B1.3)         Bacillus pumilus, in particular strain GB34 (available as Yield         Shield® from Bayer AG, DE); (B1.4) Bacillus pumilus, in         particular strain BU F-33 (having NRRL Accession No. 50185);         (B1.5) Bacillus amyloliquefaciens, in particular strain D747         (available as Double Nickel™ from Certis, US, having accession         number FERM BP-8234 and disclosed in U.S. Pat. No. 7,094,592);         (B1.6) Bacillus subtilis Y1336 (available as BIOBAC®WP from         Bion-Tech, Taiwan, registered as a biological fungicide in         Taiwan under Registration Nos. 4764, 5454, 5096 and 5277);         (B1.7) Bacillus amyloliquefaciens strain MBI 600 (available as         SUBTILEX from BASF SE); (B1.8) Bacillus subtilis strain GB03         (available as Kodiak® from Bayer AG, DE); (B1.9) Bacillus         subtilis var. amyloliquefaciens strain FZB24 (available from         Novozymes Biologicals Inc., Salem, Virginia or Syngenta Crop         Protection, LLC, Greensboro, North Carolina as the fungicide         TAEGRO® or TAEGRO© ECO (EPA Registration No. 70127-5); (B1.10)         Bacillus mycoides, isolate J (available as BmJ TGAI or WG from         Certis USA); (B1.11) Bacillus licheniformis, in particular         strain SB3086 (available as EcoGuard™ Biofungicide and Green         Releaf from Novozymes); (B1.12) a Paenibacillus sp. strain         having Accession No. NRRL B-50972 or Accession No. NRRL B-67129         and described in International Patent Publication No. WO         2016/154297,     -   (C1) fatty acids or derivatives, for example (C1.1) a         composition comprising one or more fatty acids or derivatives         thereof selected from unsaturated and saturated C₁₂-C₂₄ fatty         acids, salts thereof, esters thereof or mixtures of any of the         foregoing, wherein at least 95% of said fatty acids or         derivatives thereof are in the range of C₁₄ to C₂₀ (e.g. FLiPPER         by AlphaBio Pesticides or Bayer AG).

In some embodiments, the biological control agent is a Bacillus subtilis or Bacillus amyloliquefaciens strain that produces a fengycin or plipastatin-type compound, an iturin-type compound, and/or a surfactin-type compound. For background, see the following review article: Ongena, M., et al., “Bacillus Lipopeptides: Versatile Weapons for Plant Disease Biocontrol,” Trends in Microbiology, Vol 16, No. 3, March 2008, pp. 115-125. Bacillus strains capable of producing lipopeptides include Bacillus subtilis QST713 (available as SERENADE OPTI or SERENADE ASO from Bayer CropScience LP, US, having NRRL Accession No. B21661 and described in U.S. Pat. No. 6,060,051), Bacillus amyloliquefaciens strain D747 (available as Double Nickel™ from Certis, US, having accession number FERM BP-8234 and disclosed in U.S. Pat. No. 7,094,592); Bacillus subtilis MBI600 (available as SUBTILEX® from Becker Underwood, US EPA Reg. No. 71840-8); Bacillus subtilis Y1336 (available as BIOBAC® WP from Bion-Tech, Taiwan, registered as a biological fungicide in Taiwan under Registration Nos. 4764, 5454, 5096 and 5277); Bacillus amyloliquefaciens, in particular strain FZB42 (available as RHIZOVITAL® from ABiTEP, DE); and Bacillus subtilis var. amyloliquefaciens FZB24 (available from Novozymes Biologicals Inc., Salem, Virginia or Syngenta Crop Protection, LLC, Greensboro, North Carolina as the fungicide TAEGRO® or TAEGRO® ECO (EPA Registration No. 70127-5); and

-   -   (B2) fungi, for example: (B2.1) Coniothyrium minitans, in         particular strain CON/M/91-8 (Accession No. DSM-9660; e.g.         Contans® from Bayer); (B2.2) Metschnikowia fructicola, in         particular strain NRRL Y-30752 (e.g. Shemer®); (B2.3)         Microsphaeropsis ochracea (e.g. Microx® from Prophyta); (B2.5)         Trichoderma spp., including Trichoderma atroviride, strain SC1         described in International Application No. PCT/IT2008/000196);         (B2.6) Trichoderma harzianum rifai strain KRL-AG2 (also known as         strain T-22, /ATCC 208479, e.g. PLANTSHIELD T-22G, Rootshield®,         and TurfShield from BioWorks, US); (B2.14) Gliocladium roseum,         strain 321U from W.F. Stoneman Company LLC; (B2.35) Talaromyces         flavus, strain V117b; (B2.36) Trichoderma asperellum, strain ICC         012 from Isagro; (B2.37) Trichoderma asperellum, strain SKT-1         (e.g. ECO-HOPE® from Kumiai Chemical Industry); (B2.38)         Trichoderma atroviride, strain CNCM 1-1237 (e.g. Esquive® WP         from Agrauxine, FR); (B2.39) Trichoderma atroviride, strain no.         V08/002387; (B2.40) Trichoderma atroviride, strain NMI no.         V08/002388; (B2.41) Trichoderma atroviride, strain NMI no.         V08/002389; (B2.42) Trichoderma atroviride, strain NMI no.         V08/002390; (B2.43) Trichoderma atroviride, strain LC52 (e.g.         Tenet by Agrimm Technologies Limited); (B2.44) Trichoderma         atroviride, strain ATCC 20476 (IMI 206040); (B2.45) Trichoderma         atroviride, strain T11 (IMI352941/CECT20498); (B2.46)         Trichoderma harmatum; (B2.47) Trichoderma harzianum; (B2.48)         Trichoderma harzianum rifai T39 (e.g. Trichodex® from         Makhteshim, US); (B2.49) Trichoderma harzianum, in particular,         strain KD (e.g. Trichoplus from Biological Control Products, SA         (acquired by Becker Underwood)); (B2.50) Trichoderma harzianum,         strain ITEM 908 (e.g. Trianum-P from Koppert); (B2.51)         Trichoderma harzianum, strain TH35 (e.g. Root-Pro by Mycontrol);         (B2.52) Trichoderma virens (also known as Gliocladium virens),         in particular strain GL-21 (e.g. SoilGard 12G by Certis, US);         (B2.53) Trichoderma viride, strain TV1 (e.g. Trianum-P by         Koppert); (B2.54) Ampelomyces quisqualis, in particular strain         AQ 10 (e.g. AQ 10® by IntrachemBio Italia); (B2.56)         Aureobasidium pullulans, in particular blastospores of strain         DSM14940; (B2.57) Aureobasidium pullulans, in particular         blastospores of strain DSM 14941; (B2.58) Aureobasidium         pullulans, in particular mixtures of blastospores of strains         DSM14940 and DSM 14941 (e.g. Botector® by bio-ferm, CH); (B2.64)         Cladosporium cladosporioides, strain H39 (by Stichting Dienst         Landbouwkundig Onderzoek); (B2.69) Gliocladium catenulatum         (Synonym: Clonostachys rosea f catenulate) strain J1446 (e.g.         Prestop® by AgBio Inc. and also e.g. Primastop® by Kemira Agro         Oy); (B2.70) Lecanicillium lecanii (formerly known as         Verticillium lecanii) conidia of strain KV01 (e.g. Vertalec® by         Koppert/Arysta); (B2.71) Penicillium vermiculatum; (B2.72)         Pichia anomala, strain WRL-076 (NRRL Y-30842); (B2.75)         Trichoderma atroviride, strain SKT-1 (FERM P-16510); (B2.76)         Trichoderma atroviride, strain SKT-2 (FERM P-16511); (B2.77)         Trichoderma atroviride, strain SKT-3 (FERM P-17021); (B2.78)         Trichoderma gamsii (formerly T. viride), strain ICC080 (IMI CC         392151 CABI, e.g. BioDerma by AGROBIOSOL DE MEXICO, S.A. DE         C.V.); (B2.79) Trichoderma harzianum, strain DB 103 (e.g., T-Gro         7456 by Dagutat Biolab); (B2.80) Trichoderma polysporum, strain         IMI 206039 (e.g. Binab TF WP by BINAB Bio-Innovation AB,         Sweden); (B2.81) Trichoderma stromaticum (e.g. Tricovab by         Ceplac, Brazil); (B2.83) Ulocladium oudemansii, in particular         strain HRU3 (e.g. Botry-Zen® by Botry-Zen Ltd, NZ); (B2.84)         Verticillium albo-atrum (formerly V. dahliae), strain WCS850         (CBS 276.92; e.g. Dutch Trig by Tree Care Innovations); (B2.86)         Verticillium chlamydosporium; (B2.87) mixtures of Trichoderma         asperellum strain ICC 012 and Trichoderma gamsii strain ICC 080         (product known as e.g. BIO-TAM™ from Bayer CropScience LP, US).

Further examples of biological control agents which may be combined with the compound combination of the invention are:

bacteria selected from the group consisting of Bacillus cereus, in particular B. cereus strain CNCM I-1562 and Bacillus firmus, strain 1-1582 (Accession number CNCM 1-1582), Bacillus subtilis strain OST 30002 (Accession No. NRRL B-50421), Bacillus thuringiensis, in particular B. thuringiensis subspecies israelensis (serotype H-14), strain AM65-52 (Accession No. ATCC 1276), B. thuringiensis subsp. aizawai, in particular strain ABTS-1857 (SD-1372), B. thuringiensis subsp. kurstaki strain HD-1, B. thuringiensis subsp. tenebrionis strain NB 176 (SD-5428), Pasteuria penetrans, Pasteuria spp. (Rotylenchulus reniformis nematode)-PR3 (Accession Number ATCC SD-5834), Streptomyces microflavus strain AQ6121 (=QRD 31.013, NRRL B-50550), and Streptomyces galbus strain AQ 6047 (Accession Number NRRL 30232); fungi and yeasts selected from the group consisting of Beauveria bassiana, in particular strain ATCC 74040, Lecanicillium spp., in particular strain HRO LEC 12, Metarhizium anisopliae, in particular strain F52 (DSM3884 or ATCC 90448), Paecilomyces fumosoroseus (now: Isaria fumosorosea), in particular strain IFPC 200613, or strain Apopka 97 (Accession No. ATCC 20874), and Paecilomyces lilacinus, in particular P. lilacinus strain 251 (AGAL 89/030550); viruses selected from the group consisting of Adoxophyes orana (summer fruit tortrix) granulosis virus (GV), Cydia pomonella (codling moth) granulosis virus (GV), Helicoverpa armigera (cotton bollworm) nuclear polyhedrosis virus (NPV), Spodoptera exigua (beet armyworm) mNPV, Spodoptera frugiperda (fall armyworm) mNPV, and Spodoptera littoralis (African cotton leafworm) NPV. bacteria and fungi which can be added as ‘inoculant’ to plants or plant parts or plant organs and which, by virtue of their particular properties, promote plant growth and plant health. Examples are: Agrobacterium spp., Azorhizobium caulinodans, Azospirillum spp., Azotobacter spp., Bradyrhizobium spp., Burkholderia spp., in particular Burkholderia cepacia (formerly known as Pseudomonas cepacia), Gigaspora spp., or Gigaspora monosporum, Glomus spp., Laccaria spp., Lactobacillus buchneri, Paraglomus spp., Pisolithus tinctorus, Pseudomonas spp., Rhizobium spp., in particular Rhizobium trifolii, Rhizopogon spp., Scleroderma spp., Suillus spp., and Streptomyces spp. plant extracts and products formed by microorganisms including proteins and secondary metabolites which can be used as biological control agents, such as Allium sativum, Artemisia absinthium, azadirachtin, Biokeeper WP, Cassia nigricans, Celastrus angulatus, Chenopodium anthelminticum, chitin, Armour-Zen, Dryopteris filix-mas, Equisetum arvense, Fortune Aza, Fungastop, Heads Up (Chenopodium quinoa saponin extract), Pyrethrum/Pyrethrins, Quassia amara, Quercus, Quillaja, Regalia, “Requiem™ Insecticide”, rotenone, ryania/ryanodine, Symphytum officinale, Tanacetum vulgare, thymol, Triact 70, TriCon, Tropaeulum majus, Urtica dioica, Veratrin, Viscum album, Brassicaceae extract, in particular oilseed rape powder or mustard powder a composition comprising one or more fatty acids or derivatives thereof selected from unsaturated and saturated C₁₂-C₂₄ fatty acids, salts thereof, esters thereof or mixtures of any of the foregoing, wherein at least 95% of said fatty acids or derivatives thereof are in the range of C₁₄ to C₂₀ (e.g. FLiPPER by AlphaBio Pesticides or Bayer AG).

Examples of insecticides, acaricides and nematicides, respectively, which could be mixed with the compound combination of the invention are:

-   -   (1) Acetylcholinesterase (AChE) inhibitors, such as, for         example, carbamates, for example alanycarb, aldicarb,         bendiocarb, benfuracarb, butocarboxim, butoxycarboxim, carbaryl,         carbofuran, carbosulfan, ethiofencarb, fenobucarb, formetanate,         furathiocarb, isoprocarb, methiocarb, methomyl, metolcarb,         oxamyl, pirimicarb, propoxur, thiodicarb, thiofanox, triazamate,         trimethacarb, XMC and xylylcarb; or organophosphates, for         example acephate, azamethiphos, azinphos-ethyl, azinphos-methyl,         cadusafos, chlorethoxyfos, chlorfenvinphos, chlormephos,         chlorpyrifos-methyl, coumaphos, cyanophos, demeton-S-methyl,         diazinon, dichlorvos/DDVP, dicrotophos, dimethoate,         dimethylvinphos, disulfoton, EPN, ethion, ethoprophos, famphur,         fenamiphos, fenitrothion, fenthion, fosthiazate, heptenophos,         imicyafos, isofenphos, isopropyl O-(methoxyaminothiophosphoryl)         salicylate, isoxathion, malathion, mecarbam, methamidophos,         methidathion, mevinphos, monocrotophos, naled, omethoate,         oxydemeton-methyl, parathion-methyl, phenthoate, phorate,         phosalone, phosmet, phosphamidon, phoxim, pirimiphos-methyl,         profenofos, propetamphos, prothiofos, pyraclofos,         pyridaphenthion, quinalphos, sulfotep, tebupirimfos, temephos,         terbufos, tetrachlorvinphos, thiometon, triazophos, triclorfon         and vamidothion.     -   (2) GABA-gated chloride channel blockers, such as, for example,         cyclodiene-organochlorines, for example chlordane and endosulfan         or phenylpyrazoles (fiproles), for example ethiprole and         fipronil.     -   (3) Sodium channel modulators, such as, for example,         pyrethroids, e.g. acrinathrin, allethrin, d-cis-trans allethrin,         d-trans allethrin, bifenthrin, bioallethrin, bioallethrin         s-cyclopentenyl isomer, bioresmethrin, cycloprothrin,         cyfluthrin, beta-cyfluthrin, cyhalothrin, lambda-cyhalothrin,         gamma-cyhalothrin, cypermethrin, alpha-cypermethrin,         beta-cypermethrin, theta-cypermethrin, zeta-cypermethrin,         cyphenothrin [(1R)-trans-isomer], deltamethrin, empenthrin         [(EZ)-(1R)-isomer], esfenvalerate, etofenprox, fenpropathrin,         fenvalerate, flucythrinate, flumethrin, tau-fluvalinate,         halfenprox, imiprothrin, kadethrin, momfluorothrin, permethrin,         phenothrin [(1R)-trans-isomer], prallethrin, pyrethrins         (pyrethrum), resmethrin, silafluofen, tefluthrin, tetramethrin,         tetramethrin [(1R)-isomer)], tralomethrin and transfluthrin or         DDT or methoxychlor.     -   (4) Nicotinic acetylcholine receptor (nAChR) competitive         modulators, such as, for example, neonicotinoids, e.g.         acetamiprid, clothianidin, dinotefuran, imidacloprid,         nitenpyram, thiacloprid and thiamethoxam or nicotine or         sulfoxaflor or flupyradifurone.     -   (5) Nicotinic acetylcholine receptor (nAChR) allosteric         modulators, such as, for example, spinosyns, e.g. spinetoram and         spinosad.     -   (6) Glutamate-gated chloride channel (GluCl) allosteric         modulators, such as, for example, avermectins/milbemycins, for         example abamectin, emamectin benzoate, lepimectin and         milbemectin.     -   (7) Juvenile hormone mimics, such as, for example, juvenile         hormone analogues, e.g. hydroprene, kinoprene and methoprene or         fenoxycarb or pyriproxyfen.     -   (8) Miscellaneous non-specific (multi-site) inhibitors, such as,         for example, alkyl halides, e.g. methyl bromide and other alkyl         halides; or chloropicrine or sulphuryl fluoride or borax or         tartar emetic or methyl isocyanate generators, e.g. diazomet and         metam.     -   (9) Modulators of Chordotonal Organs, such as, for example         pymetrozine or flonicamid.     -   (10) Mite growth inhibitors, such as, for example clofentezine,         hexythiazox and diflovidazin or etoxazole.     -   (11) Microbial disruptors of the insect gut membrane, such as,         for example Bacillus thuringiensis subspecies israelensis,         Bacillus sphaericus, Bacillus thuringiensis subspecies aizawai,         Bacillus thuringiensis subspecies kurstaki, Bacillus         thuringiensis subspecies tenebrionis, and B.t. plant proteins:         Cry1Ab, Cry1Ac, Cry1Fa, Cry1A.105, Cry2Ab, Vip3A, mCry3A,         Cry3Ab, Cry3Bb, Cry34Ab1/35Ab1.     -   (12) Inhibitors of mitochondrial ATP synthase, such as, ATP         disruptors such as, for example, diafenthiuron or organotin         compounds, for example azocyclotin, cyhexatin and fenbutatin         oxide or propargite or tetradifon.     -   (13) Uncouplers of oxidative phosphorylation via disruption of         the proton gradient, such as, for example, chlorfenapyr, DNOC         and sulfluramid.     -   (14) Nicotinic acetylcholine receptor channel blockers, such as,         for example, bensultap, cartap hydrochloride, thiocylam, and         thiosultap-sodium.     -   (15) Inhibitors of chitin biosynthesis, type 0, such as, for         example, bistrifluron, chlorfluazuron, diflubenzuron,         flucycloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron,         noviflumuron, teflubenzuron and triflumuron.     -   (16) Inhibitors of chitin biosynthesis, type 1, for example         buprofezin.     -   (17) Moulting disruptor (in particular for Diptera, i.e.         dipterans), such as, for example, cyromazine.     -   (18) Ecdysone receptor agonists, such as, for example,         chromafenozide, halofenozide, methoxyfenozide and tebufenozide.     -   (19) Octopamine receptor agonists, such as, for example,         amitraz.     -   (20) Mitochondrial complex III electron transport inhibitors,         such as, for example, hydramethylnone or acequinocyl or         fluacrypyrim.     -   (21) Mitochondrial complex I electron transport inhibitors, such         as, for example from the group of the METI acaricides, e.g.         fenazaquin, fenpyroximate, pyrimidifen, pyridaben, tebufenpyrad         and tolfenpyrad or rotenone (Derris).     -   (22) Voltage-dependent sodium channel blockers, such as, for         example indoxacarb or metaflumizone.     -   (23) Inhibitors of acetyl CoA carboxylase, such as, for example,         tetronic and tetramic acid derivatives, e.g. spirodiclofen,         spiromesifen and spirotetramat.     -   (24) Mitochondrial complex IV electron transport inhibitors,         such as, for example, phosphines, e.g. aluminium phosphide,         calcium phosphide, phosphine and zinc phosphide or cyanides,         e.g. calcium cyanide, potassium cyanide and sodium cyanide.     -   (25) Mitochondrial complex II electron transport inhibitors,         such as, for example, beta-ketonitrile derivatives, e.g.         cyenopyrafen and cyflumetofen and carboxanilides, such as, for         example, pyflubumide.     -   (28) Ryanodine receptor modulators, such as, for example,         diamides, e.g. chlorantraniliprole, cyantraniliprole and         flubendiamide,         further active compounds such as, for example, Afidopyropen,         Afoxolaner, Azadirachtin, Benclothiaz, Benzoximate, Bifenazate,         Broflanilide, Bromopropylate, Chinomethionat, Chloroprallethrin,         Cryolite, Cyclaniliprole, Cycloxaprid, Cyhalodiamide,         Dicloromezotiaz, Dicofol, epsilon-Metofluthrin,         epsilon-Momfluthrin, Flometoquin, Fluazaindolizine,         Fluensulfone, Flufenerim, Flufenoxystrobin, Flufiprole,         Fluhexafon, Fluopyram, Fluralaner, Fluxametamide, Fufenozide,         Guadipyr, Heptafluthrin, Imidaclothiz, Iprodione,         kappa-Bifenthrin, kappa-Tefluthrin, Lotilaner, Meperfluthrin,         Paichongding, Pyridalyl, Pyrifluquinazon, Pyriminostrobin,         Spirobudiclofen, Tetramethylfluthrin, Tetraniliprole,         Tetrachlorantraniliprole, Tigolaner, Tioxazafen, Thiofluoximate,         Triflumezopyrim and iodomethane; furthermore preparations based         on Bacillus firmus (1-1582, BioNeem, Votivo), and also the         following compounds:         1-{2-fluoro-4-methyl-5-[(2,2,2-trifluoroethyl)sulphinyl]phenyl}-3-(trifluoromethyl)-1H-1,2,4-triazole-5-amine         (known from WO2006/043635) (CAS 885026-50-6),         {1′-[(2E)-3-(4-chlorophenyl)prop-2-en-1-yl]-5-fluorospiro[indol-3,4′-piperidin]-1(2H)-yl}(2-chloropyridin-4-yl)methanone         (known from WO2003/106457) (CAS 637360-23-7),         2-chloro-N-[2-{1-[(2E)-3-(4-chlorophenyl)prop-2-en-1-yl]piperidin-4-yl}-4-(trifluoromethyl)phenyl]isonicotinamide         (known from WO2006/003494) (CAS 872999-66-1),         3-(4-chloro-2,6-dimethylphenyl)-4-hydroxy-8-methoxy-1,8-diazaspiro[4.5]dec-3-en-2-one         (known from WO 2010052161) (CAS 1225292-17-0),         3-(4-chloro-2,6-dimethylphenyl)-8-methoxy-2-oxo-1,8-diazaspiro[4.5]dec-3-en-4-yl         ethyl carbonate (known from EP2647626) (CAS 1440516-42-6),         4-(but-2-yn-1-yloxy)-6-(3,5-dimethylpiperidin-1-yl)-5-fluoropyrimidine         (known from WO2004/099160) (CAS 792914-58-0), PF1364 (known from         JP2010/018586) (CAS 1204776-60-2),         N-[(2E)-1-[(6-chloropyridin-3-yl)methyl]pyridin-2(1H)-ylidene]-2,2,2-trifluoroacetamide         (known from WO2012/029672) (CAS 1363400-41-2),         (3E)-3-[1-[(6-chloro-3-pyridyl)methyl]-2-pyridylidene]-1,1,1-trifluoro-propan-2-one         (known from WO2013/144213) (CAS 1461743-15-6),         N-[3-(benzylcarbamoyl)-4-chlorophenyl]-1-methyl-3-(pentafluoroethyl)-4-(trifluoromethyl)-1H-pyrazole-5-carboxamide         (known from WO2010/051926) (CAS 1226889-14-0),         5-bromo-4-chloro-N-[4-chloro-2-methyl-6-(methylcarbamoyl)phenyl]-2-(3-chloro-2-pyridyl)pyrazole-3-carboxamide         (known from CN103232431) (CAS 1449220-44-3),         4-[5-(3,5-dichlorophenyl)-4,5-dihydro-5-(trifluoromethyl)-3-isoxazolyl]-2-methyl-N-(cis-1-oxido-3-thietanyl)-benzamide,         4-[5-(3,5-dichlorophenyl)-4,5-dihydro-5-(trifluoromethyl)-3-isoxazolyl]-2-methyl-N-(trans-1-oxido-3-thietanyl)-benzamide         and         4-[(5S)-5-(3,5-dichlorophenyl)-4,5-dihydro-5-(trifluoromethyl)-3-isoxazolyl]-2-methyl-N-(cis-1-oxido-3-thietanyl)benzamide         (known from WO 2013/050317 A1) (CAS 1332628-83-7),         N-[3-chloro-1-(3-pyridinyl)-1H-pyrazol-4-yl]-N-ethyl-3-[(3,3,3-trifluoropropyl)sulfinyl]-propanamide,         (+)-N-[3-chloro-1-(3-pyridinyl)-1H-pyrazol-4-yl]-N-ethyl-3-[(3,3,3-trifluoropropyl)sulfinyl]-propanamide         and         (−)-N-[3-chloro-1-(3-pyridinyl)-1H-pyrazol-4-yl]-N-ethyl-3-[(3,3,3-trifluoropropyl)sulfinyl]-propanamide         (known from WO 2013/162715 A2, WO 2013/162716 A2, US         2014/0213448 A1) (CAS 1477923-37-7),         5-[[(2E)-3-chloro-2-propen-1-yl]amino]-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-[(trifluoromethyl)sulfinyl]-1H-pyrazole-3-carbonitrile         (known from CN 101337937 A) (CAS 1105672-77-2),         3-bromo-N-[4-chloro-2-methyl-6-[(methylamino)thioxomethyl]phenyl]-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxamide,         (Liudaibenjiaxuanan, known from CN 103109816 A) (CAS         1232543-85-9);         N-[4-chloro-2-[[(1,1-dimethylethyl)amino]carbonyl]-6-methylphenyl]-1-(3-chloro-2-pyridinyl)-3-(fluoromethoxy)-1H-Pyrazole-5-carboxamide         (known from WO 2012/034403 A1) (CAS 1268277-22-0),         N-[2-(5-amino-1,3,4-thiadiazol-2-yl)-4-chloro-6-methylphenyl]-3-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxamide         (known from WO 2011/085575 A1) (CAS 1233882-22-8),         4-[3-[2,6-dichloro-4-[(3,3-dichloro-2-propen-1-yl)oxy]phenoxy]propoxy]-2-methoxy-6-(trifluoromethyl)-pyrimidine         (known from CN 101337940 A) (CAS 1108184-52-6); (2E)- and         2(Z)-2-[2-(4-cyanophenyl)-1-[3-(trifluoromethyl)phenyl]ethylidene]-N-[4-(difluoromethoxy)phenyl]-hydrazinecarboxamide         (known from CN 101715774 A) (CAS 1232543-85-9);         3-(2,2-dichloroethenyl)-2,2-dimethyl-4-(1H-benzimidazol-2-yl)phenyl-cyclopropanecarboxylic         acid ester (known from CN 103524422 A) (CAS 1542271-46-4);         (4aS)-7-chloro-2,5-dihydro-2-[[(methoxycarbonyl) 10         [4-[(trifluoromethyl)thio]phenyl]amino]carbonyl]-indeno[1,2-e][1,3,4]oxadiazine-4a(3H)-carboxylic         acid methyl ester (known from CN 102391261 A) (CAS         1370358-69-2); 6-deoxy-3-O-ethyl-2,4-di-O-methyl-,         1-[N-[4-[1-[4-(1,1,2,2,2-pentafluoroethoxy)phenyl]-1H-1,2,4-triazol-3-yl]phenyl]carbamate]-α-L-mannopyranose         (known from US 2014/0275503 A1) (CAS 1181213-14-8);         8-(2-cyclopropylmethoxy-4-trifluoromethyl-phenoxy)-3-(6-trifluoromethyl-pyridazin-3-yl)-3-aza-bicyclo[3.2.1]octane         (CAS 1253850-56-4),         (8-anti)-8-(2-cyclopropylmethoxy-4-trifluoromethyl-phenoxy)-3-(6-trifluoromethyl-pyridazin-3-yl)-3-aza-bicyclo[3.2.1]octane         (CAS 933798-27-7),         (8-syn)-8-(2-cyclopropylmethoxy-4-trifluoromethyl-phenoxy)-3-(6-trifluoromethyl-pyridazin-3-yl)-3-aza-bicyclo[3.2.1]octane         (known from WO 2007040280 A1, WO 2007040282 A1) (CAS         934001-66-8),         N-[3-chloro-1-(3-pyridinyl)-1H-pyrazol-4-yl]-N-ethyl-3-[(3,3,3-trifluoropropyl)thio]-propanamide         (known from WO 2015/058021 A1, WO 2015/058028 A1) (CAS         1477919-27-9) and         N-[4-(aminothioxomethyl)-2-methyl-6-[(methylamino)carbonyl]phenyl]-3-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxamide         (known from CN 103265527 A) (CAS 1452877-50-7),         5-(1,3-dioxan-2-yl)-4-[[4-(trifluoromethyl)phenyl]methoxy]-pyrimidine         (known from WO 2013/115391 A1) (CAS 1449021-97-9),         3-(4-chloro-2,6-dimethylphenyl)-4-hydroxy-8-methoxy-1-methyl-1,8-diazaspiro[4.5]dec-3-en-2-one         (known from WO 2010/066780 A1, WO 2011/151146 A1) (CAS         1229023-34-0),         3-(4-chloro-2,6-dimethylphenyl)-8-methoxy-1-methyl-1,8-diazaspiro[4.5]decane-2,4-dione         (known from WO 2014/187846 A1) (CAS 1638765-58-8),         3-(4-chloro-2,6-dimethylphenyl)-8-methoxy-1-methyl-2-oxo-1,8-diazaspiro[4.5]dec-3-en-4-yl-carbonic         acid ethyl ester (known from WO 2010/066780 A1, WO 2011151146         A1) (CAS 1229023-00-0),         N-[1-[(6-chloro-3-pyridinyl)methyl]-2(1H)-pyridinylidene]-2,2,2-trifluoro-acetamide         (known from DE 3639877 A1, WO 2012029672 A1) (CAS 1363400-41-2),         [N(E)]-N-[1-[(6-chloro-3-pyridinyl)methyl]-2(1H)-pyridinylidene]-2,2,2-trifluoro-acetamide,         (known from WO 2016005276 A1) (CAS 1689566-03-7),         [N(Z)]—N-[1-[(6-chloro-3-pyridinyl)methyl]-2(1H)-pyridinylidene]-2,2,2-trifluoro-acetamide,         (CAS 1702305-40-5),         3-endo-3-[2-propoxy-4-(trifluoromethyl)phenoxy]-9-[[5-(trifluoromethyl)-2-pyridinyl]oxy]-9-azabicyclo[3.3.1]nonane         (known from WO 2011/105506 A1, WO 2016/133011 A1) (CAS         1332838-17-1).

Examples of safeners which could be mixed with the compound combination of the invention are, for example, benoxacor, cloquintocet (-mexyl), cyometrinil, cyprosulfamide, dichlormid, fenchlorazole (-ethyl), fenclorim, flurazole, fluxofenim, furilazole, isoxadifen (-ethyl), mefenpyr (-diethyl), naphthalic anhydride, oxabetrinil, 2-methoxy-N-({4-[(methylcarbamoyl)amino]phenyl}-sulphonyl)benzamide (CAS 129531-12-0), 4-(dichloroacetyl)-1-oxa-4-azaspiro[4.5]decane (CAS 71526-07-3), 2,2,5-trimethyl-3-(dichloroacetyl)-1,3-oxazolidine (CAS 52836-31-4).

Examples of herbicides which could be mixed with the compound combination of the invention are:

Acetochlor, acifluorfen, acifluorfen-sodium, aclonifen, alachlor, allidochlor, alloxydim, alloxydim-sodium, ametryn, amicarbazone, amidochlor, amidosulfuron, 4-amino-3-chloro-5-fluoro-6-(7-fluoro-1H-indol-6-yl)pyridine-2-carboxylic acid, aminocyclopyrachlor, aminocyclopyrachlor-potassium, aminocyclo-pyrachlor-methyl, aminopyralid, amitrole, ammoniumsulfamate, anilofos, asulam, atrazine, azafenidin, azimsulfuron, beflubutamid, benazolin, benazolin-ethyl, benfluralin, benfuresate, bensulfuron, bensulfuron-methyl, bensulide, bentazone, benzobicyclon, benzofenap, bicyclopyron, bifenox, bilanafos, bilanafos-sodium, bispyribac, bispyribac-sodium, bixlozone, bromacil, bromobutide, bromofenoxim, bromoxynil, bromoxynil-butyrate, -potassium, -heptanoate, and -octanoate, busoxinone, butachlor, butafenacil, butamifos, butenachlor, butralin, butroxydim, butylate, cafenstrole, carbetamide, carfentrazone, carfentrazone-ethyl, chloramben, chlorbromuron, 1-{2-chloro-3-[(3-cyclopropyl-5-hydroxy-1-methyl-1H-pyrazol-4-yl)carbonyl]-6-(trifluormethyl)phenyl}piperidin-2-on, 4-{2-chloro-3-[(3,5-dimethyl-1H-pyrazol-1-yl)methyl]-4-(methylsulfonyl)benzoyl}-1,3-dimethyl-1H-pyrazol-5-yl-1,3-dimethyl-1H-pyrazol-4-carboxylat, chlorfenac, chlorfenac-sodium, chlorfenprop, chlorflurenol, chlorflurenol-methyl, chloridazon, chlorimuron, chlorimuron-ethyl, 2-[2-chloro-4-(methylsulfonyl)-3-(morpholin-4ylmethyl)benzoyl}-3-hydroxycyclohex-2-en-1-on, 4-{2-chloro-4-(methylsulfonyl)-3-[(2,2,2-trifluorethoxy)methyl]benzoyl}-1-ethyl-1H-pyrazol-5-yl-1,3-dimethyl-1H,pyrazol-4-carboxylat, chlorophthalim, chlorotoluron, chlorthal-dimethyl, 3-[5-chloro-4-(trifluormethyl)pyridine-2-yl]-4-hydroxy-1-methylimidazolidine-2-on, chlorsulfuron, cinidon, cinidon-ethyl, cinmethylin, cinosulfuron, clacyfos, clethodim, clodinafop, clodinafop-propargyl, clomazone, clomeprop, clopyralid, cloransulam, cloransulam-methyl, cumyluron, cyanamide, cyanazine, cycloate, cyclopyranil, cyclopyrimorate, cyclosulfamuron, cycloxydim, cyhalofop, cyhalofop-butyl, cyprazine, 2,4-D, 2,4-D-butotyl, -butyl, -dimethylammonium, -diolamin, -ethyl, -2-ethylhexyl, -isobutyl, -isooctyl, -isopropylammonium, -potassium, -triisopropanolammonium, and -trolamine, 2,4-DB, 2,4-DB-butyl, -dimethylammonium, -isooctyl, -potassium, and -sodium, daimuron (dymron), dalapon, dazomet, n-decanol, desmedipham, detosyl-pyrazolate (DTP), dicamba, dichlobenil, 2-(2,4-dichlorobenzyl)-4,4-dimethyl-1,2-oxazolidin-3-one, 2-(2,5-dichlorobenzyl)-4,4-dimethyl-1,2-oxazolidin-3-one, dichlorprop, dichlorprop-P, diclofop, diclofop-methyl, diclofop-P-methyl, diclosulam, difenzoquat, diflufenican, diflufenzopyr, diflufenzopyr-sodium, dimefuron, dimepiperate, dimethachlor, dimethametryn, dimethenamid, dimethenamid-P, 3-(2,6-dimethylphenyl)-6-[(2-hydroxy-6-oxocyclohex-1-en-1-yl)carbonyl]-1-methylchinazolin-2,4(1H,3H)-dion, 1,3-dimethyl-4-[2-(methylsulfonyl)-4-(trifluormethyl)benzoyl]-1H-pyrazol-5-yl-1,3-dimethyl-1H-pyrazol-4-carboxylat, dimetrasulfuron, dinitramine, dinoterb, diphenamid, diquat, diquat-dibromid, dithiopyr, diuron, DMPA, DNOC, endothal, EPTC, esprocarb, ethalfluralin, ethametsulfuron, ethametsulfuron-methyl, ethiozin, ethofumesate, ethoxyfen, ethoxyfen-ethyl, ethoxysulfuron, etobenzanid, ethyl-[(3-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluormethyl)-3,6-dihydropyrimidin-1(2H)-yl]phenoxy}pyridine-2-yl)oxy]acetat, F-9960, F-5231, i.e. N-{2-chloro-4-fluoro-5-[4-(3-fluoropropyl)-5-oxo-4,5-dihydro-1H-tetrazol-1-yl]phenyl}ethanesulfonamide, F-7967, i. e. 3-[7-chloro-5-fluoro-2-(trifluoromethyl)-1H-benzimidazol-4-yl]-1-methyl-6-(trifluoromethyl)pyrimidine-2,4(1H,3H)-dione, fenoxaprop, fenoxaprop-P, fenoxaprop-ethyl, fenoxaprop-P-ethyl, fenoxasulfone, fenquinotrione, fentrazamide, flamprop, flamprop-M-isopropyl, flamprop-M-methyl, flazasulfuron, florasulam, fluazifop, fluazifop-P, fluazifop-butyl, fluazifop-P-butyl, flucarbazone, flucarbazone-sodium, flucetosulfuron, fluchloralin, flufenacet, flufenpyr, flufenpyr-ethyl, flumetsulam, flumiclorac, flumiclorac-pentyl, flumioxazin, fluometuron, flurenol, flurenol-butyl, -dimethylammonium and -methyl, fluoroglycofen, fluoroglycofen-ethyl, flupropanate, flupyrsulfuron, flupyrsulfuron-methyl-sodium, fluridone, flurochloridone, fluroxypyr, fluroxypyr-meptyl, flurtamone, fluthiacet, fluthiacet-methyl, fomesafen, fomesafen-sodium, foramsulfuron, fosamine, glufosinate, glufosinate-ammonium, glufosinate-P-sodium, glufosinate-P-ammonium, glufosinate-P-sodium, glyphosate, glyphosate-ammonium, -isopropylammonium, -diammonium, -dimethylammonium, -potassium, -sodium, and -trimesium, H-9201, i.e. O-(2,4-dimethyl-6-nitrophenyl)O-ethyl isopropylphosphoramidothioate, halauxifen, halauxifen-methyl, halosafen, halosulfuron, halosulfuron-methyl, haloxyfop, haloxyfop-P, haloxyfop-ethoxyethyl, haloxyfop-P-ethoxyethyl, haloxyfop-methyl, haloxyfop-P-methyl, hexazinone, HW-02, i.e. 1-(dimethoxyphosphoryl) ethyl-(2,4-dichlorophenoxy)acetate, 4-hydroxy-1-methoxy-5-methyl-3-[4-trifluormethyl)pyridine-2-yl]imidazolidine-2-on, 4-hydroxy-1-methyl-3-[4-trifluormethyl)pyridine-2-yl]imidazolidine-2-on, (5-hydroxy-1-methyl-1H-pyrazol-4-yl)(3,3,4-trimethyl-1,1-dioxido-2,3-dihydro-1-benzothiophen-5-yl)methanon, 6-[(2-hydroxy-6-oxocyclohex-1-en-1-yl)carbonyl]-1,5-dimethyl-3-(2-methylphenyl)chinazolin-2,4(1H,3H)-dion, imazamethabenz, imazamethabenz-methyl, imazamox, imazamox-ammonium, imazapic, imazapic-ammonium, imazapyr, imazapyr-isopropylammonium, imazaquin, imazaquin-ammonium, imazethapyr, imazethapyr-immonium, imazosulfuron, indanofan, indaziflam, iodosulfuron, iodosulfuron-methyl-sodium, ioxynil, ioxynil-octanoate, -potassium and -sodium, ipfencarbazone, isoproturon, isouron, isoxaben, isoxaflutole, karbutilate, KUH-043, i.e. 3-({[5-(difluoromethyl)-1-methyl-3-(trifluoromethyl)-1H-pyrazol-4-yl]methyl}sulfonyl)-5,5-dimethyl-4,5-dihydro-1,2-oxazole, ketospiradox, lactofen, lenacil, linuron, MCPA, MCPA-butotyl, -dimethylammonium, -2-ethylhexyl, -isopropylammonium, -potassium, and -sodium, MCPB, MCPB-methyl, -ethyl, and -sodium, mecoprop, mecoprop-sodium, and -butotyl, mecoprop-P, mecoprop-P-butotyl, -dimethylammonium, -2-ethylhexyl, and -potassium, mefenacet, mefluidide, mesosulfuron, mesosulfuron-methyl, mesotrione, methabenzthiazuron, metam, metamifop, metamitron, metazachlor, metazosulfuron, methabenzthiazuron, methiopyrsulfuron, methiozolin, 2-({2-[(2-methoxyethoxy)methyl]-6-(trifluormethyl)pyridine-3-yl}carbonyl)cyclohexan-1,3-dion, methyl isothiocyanate, 1-methyl-4-[(3,3,4-trimethyl-1,1-dioxido-2,3-dihydro-1-benzothiophen-5-yl)carbonyl]-1H-pyrazol-5-ylpropan-1-sulfonat, metobromuron, metolachlor, S-metolachlor, metosulam, metoxuron, metribuzin, metsulfuron, metsulfuron-methyl, molinat, monolinuron, monosulfuron, monosulfuron-ester, MT-5950, i.e. N-(3-chloro-4-isopropylphenyl)-2-methylpentan amide, NGGC-011, napropamide, NC-310, i.e. [5-(benzyloxy)-1-methyl-1H-pyrazol-4-yl](2,4-dichlorophenyl)methanone, neburon, nicosulfuron, nonanoic acid (pelargonic acid), norflurazon, oleic acid (fatty acids), orbencarb, orthosulfamuron, oryzalin, oxadiargyl, oxadiazon, oxasulfuron, oxaziclomefon, oxyfluorfen, paraquat, paraquat dichloride, pebulate, pendimethalin, penoxsulam, pentachlorphenol, pentoxazone, pethoxamid, petroleum oils, phenmedipham, picloram, picolinafen, pinoxaden, piperophos, pretilachlor, primisulfuron, primisulfuron-methyl, prodiamine, profoxydim, prometon, prometryn, propachlor, propanil, propaquizafop, propazine, propham, propisochlor, propoxycarbazone, propoxycarbazone-sodium, propyrisulfuron, propyzamide, prosulfocarb, prosulfuron, pyraclonil, pyraflufen, pyraflufen-ethyl, pyrasulfotole, pyrazolynate (pyrazolate), pyrazosulfuron, pyrazosulfuron-ethyl, pyrazoxyfen, pyribambenz, pyribambenz-isopropyl, pyribambenz-propyl, pyribenzoxim, pyributicarb, pyridafol, pyridate, pyriftalid, pyriminobac, pyriminobac-methyl, pyrimisulfan, pyrithiobac, pyrithiobac-sodium, pyroxasulfone, pyroxsulam, quinclorac, quinmerac, quinoclamine, quizalofop, quizalofop-ethyl, quizalofop-P, quizalofop-P-ethyl, quizalofop-P-tefuryl, QYM-201, QYR-301, rimsulfuron, saflufenacil, sethoxydim, siduron, simazine, simetryn, SL-261, sulcotrion, sulfentrazone, sulfometuron, sulfometuron-methyl, sulfosulfuron, SYN-523, SYP-249, i.e. 1-ethoxy-3-methyl-1-oxobut-3-en-2-yl 5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoate, SYP-300, i.e. 1-[7-fluoro-3-oxo-4-(prop-2-yn-1-yl)-3,4-dihydro-2H-1,4-benzoxazin-6-yl]-3-propyl-2-thioxoimidazolidine-4,5-dione, 2,3,6-TBA, TCA (trichloroacetic acid), TCA-sodium, tebuthiuron, tefuryltrione, tembotrione, tepraloxydim, terbacil, terbucarb, terbumeton, terbuthylazin, terbutryn, tetflupyrolimet, thenylchlor, thiazopyr, thiencarbazone, thiencarbazone-methyl, thifensulfuron, thifensulfuron-methyl, thiobencarb, tiafenacil, tolpyralate, topra-mezone, tralkoxydim, triafamone, tri-allate, triasulfuron, triaziflam, tribenuron, tribenuron-methyl, triclopyr, trietazine, trifloxysulfuron, trifloxysulfuron-sodium, trifludimoxazin, trifluralin, triflusulfuron, triflusulfuron-methyl, tritosulfuron, urea sulfate, vernolate, XDE-848, ZJ-0862, i.e. 3,4-dichloro-N-{2-[(4,6-dimethoxypyrimidin-2-yl)oxy]benzyl}aniline.

Examples for plant growth regulators are:

Acibenzolar, acibenzolar-S-methyl, 5-aminolevulinic acid, ancymidol, 6-benzylaminopurine, Brassinolid, catechine, chlormequat chloride, cloprop, cyclanilide, 3-(cycloprop-1-enyl) propionic acid, daminozide, dazomet, n-decanol, dikegulac, dikegulac-sodium, endothal, endothal-dipotassium, -disodium, and -mono(N,N-dimethylalkylammonium), ethephon, flumetralin, flurenol, flurenol-butyl, flurprimidol, forchlorfenuron, gibberellic acid, inabenfide, indol-3-acetic acid (IAA), 4-indol-3-ylbutyric acid, isoprothiolane, probenazole, jasmonic acid, maleic hydrazide, mepiquat chloride, 1-methylcyclopropene, methyl jasmonate, 2-(1-naphthyl)acetamide, 1-naphthylacetic acid, 2-naphthyloxyacetic acid, nitrophenolate-mixture, paclobutrazol, N-(2-phenylethyl)-beta-alanine, N-phenylphthalamic acid, prohexadione, prohexadione-calcium, prohydrojasmone, salicylic acid, strigolactone, tecnazene, thidiazuron, triacontanol, trinexapac, trinexapac-ethyl, tsitodef, uniconazole, uniconazole-P.

Methods and Uses

The compound combination and the composition of the invention have potent microbicidal activity and/or plant defense modulating potential. They can be used for controlling unwanted microorganisms, such as unwanted fungi and bacteria, on plants. They can be particularly useful in crop protection (they control microorganisms that cause plants diseases) or for protecting materials (e.g. industrial materials, timber, storage goods) as described in more details herein below. More specifically, compound combination and the composition of the invention can be used to protect seeds, germinating seeds, emerged seedlings, plants, plant parts, fruits, harvest goods and/or the soil in which the plants grow from unwanted microorganisms.

Control or controlling as used herein encompasses protective, curative and eradicative treatment of unwanted microorganisms. Unwanted microorganisms may be pathogenic bacteria, pathogenic virus, pathogenic oomycetes or pathogenic fungi, more specifically phytopathogenic bacteria, phytopathogenic virus, phytopathogenic oomycetes or phytopathogenic fungi. As detailed herein below, these phytopathogenic microorganisms are the causal agents of a broad spectrum of plants diseases.

More specifically, the compound combination and the composition of the invention can be used as fungicides. For the purpose of the specification, the term “fungicide” refers to a compound or composition that can be used in crop protection for the control of unwanted fungi, such as Plasmodiophoromycetes, Chytridiomycetes, Zygomycetes, Ascomycetes, Basidiomycetes and Deuteromycetes and/or for the control of Oomycetes.

The compound combination and the composition of the invention may also be used as antibacterial agent. In particular, they may be used in crop protection, for example for the control of unwanted bacteria, such as Pseudomonadaceae, Rhizobiaceae, Xanthomonadaceae, Enterobacteriaceae, Corynebacteriaceae and Streptomycetaceae.

The present invention also relates to a method for controlling unwanted microorganisms, such as unwanted fungi, oomycetes and bacteria, on plants comprising the step of applying the compound combination or the composition of the invention to the microorganisms and/or their habitat (to the plants, plant parts, seeds, fruits or to the soil in which the plants grow), wherein the compounds (A) and (B) may be applied in a simultaneous, separate or sequential manner. If the single compounds are applied in a sequential manner, i.e. at different times, they are applied one after the other within a reasonably short period, such as a few hours or days.

Typically, when the compound combination and the composition of the invention are used in curative or protective methods for controlling phytopathogenic fungi and/or phytopathogenic oomycetes, an effective and plant-compatible amount thereof is applied to the plants, plant parts, fruits, seeds or to the soil or substrates in which the plants grow. Suitable substrates that may be used for cultivating plants include inorganic based substrates, such as mineral wool, in particular stone wool, perlite, sand or gravel; organic substrates, such as peat, pine bark or sawdust; and petroleum based substrates such as polymeric foams or plastic beads. Effective and plant-compatible amount means an amount that is sufficient to control or destroy the fungi present or liable to appear on the cropland and that does not entail any appreciable symptom of phytotoxicity for said crops. Such an amount can vary within a wide range depending on the fungus to be controlled, the type of crop, the crop growth stage, the climatic conditions and the respective compound or composition of the invention used. This amount can be determined by systematic field trials that are within the capabilities of a person skilled in the art.

Plants and Plant Parts

The compound combination and the composition of the invention may be applied to any plants or plant parts.

Plants mean all plants and plant populations, such as desired and undesired wild plants or crop plants (including naturally occurring crop plants). Crop plants may be plants which can be obtained by conventional breeding and optimization methods or by biotechnological and genetic engineering methods or combinations of these methods, including the genetically modified plants (GMO or transgenic plants) and the plant cultivars which are protectable and non-protectable by plant breeders' rights.

Genetically Modified Plants (GMO)

Genetically modified plants (GMO or transgenic plants) are plants in which a heterologous gene has been stably integrated into the genome. The expression “heterologous gene” essentially means a gene which is provided or assembled outside the plant and when introduced in the nuclear, chloroplastic or mitochondrial genome. This gene gives the transformed plant new or improved agronomic or other properties by expressing a protein or polypeptide of interest or by downregulating or silencing other gene(s) which are present in the plant (using for example, antisense technology, cosuppression technology, RNA interference—RNAi—technology or microRNA—miRNA—technology). A heterologous gene that is located in the genome is also called a transgene. A transgene that is defined by its particular location in the plant genome is called a transformation or transgenic event.

Plant cultivars are understood to mean plants which have new properties (“traits”) and have been obtained by conventional breeding, by mutagenesis or by recombinant DNA techniques. They can be cultivars, varieties, bio- or genotypes.

Plant parts are understood to mean all parts and organs of plants above and below the ground, such as shoots, leaves, needles, stalks, stems, flowers, fruit bodies, fruits, seeds, roots, tubers and rhizomes. The plant parts also include harvested material and vegetative and generative propagation material, for example cuttings, tubers, rhizomes, slips and seeds.

Plants which may be treated in accordance with the methods of the invention include the following: cotton, flax, grapevine, fruit, vegetables, such as Rosaceae sp. (for example pome fruits such as apples and pears, but also stone fruits such as apricots, cherries, almonds and peaches, and soft fruits such as strawberries), Ribesioidae sp., Juglandaceae sp., Betulaceae sp., Anacardiaceae sp., Fagaceae sp., Moraceae sp., Oleaceae sp., Actinidaceae sp., Lauraceae sp., Musaceae sp. (for example banana trees and plantations), Rubiaceae sp. (for example coffee), Theaceae sp., Sterculiceae sp., Rutaceae sp. (for example lemons, oranges and grapefruit); Solanaceae sp. (for example tomatoes), Liliaceae sp., Asteraceae sp. (for example lettuce), Umbelliferae sp., Cruciferae sp., Chenopodiaceae sp., Cucurbitaceae sp. (for example cucumber), Alliaceae sp. (for example leek, onion), Papilionaceae sp. (for example peas); major crop plants, such as Gramineae sp. (for example maize, turf, cereals such as wheat, rye, rice, barley, oats, millet and triticale), Asteraceae sp. (for example sunflower), Brassicaceae sp. (for example white cabbage, red cabbage, broccoli, cauliflower, Brussels sprouts, pak choi, kohlrabi, radishes, and oilseed rape, mustard, horseradish and cress), Fabacae sp. (for example bean, peanuts), Papilionaceae sp. (for example soya bean), Solanaceae sp. (for example potatoes), Chenopodiaceae sp. (for example sugar beet, fodder beet, swiss chard, beetroot); useful plants and ornamental plants for gardens and wooded areas; and genetically modified varieties of each of these plants.

Plants and plant cultivars which may be treated by the above disclosed methods include plants and plant cultivars which are resistant against one or more biotic stresses, i.e. said plants show a better defense against animal and microbial pests, such as against nematodes, insects, mites, phytopathogenic fungi, bacteria, viruses and/or viroids.

Plants and plant cultivars which may be treated by the above disclosed methods include those plants which are resistant to one or more abiotic stresses. Abiotic stress conditions may include, for example, drought, cold temperature exposure, heat exposure, osmotic stress, flooding, increased soil salinity, increased mineral exposure, ozone exposure, high light exposure, limited availability of nitrogen nutrients, limited availability of phosphorus nutrients, shade avoidance.

Plants and plant cultivars which may be treated by the above disclosed methods include those plants characterized by enhanced yield characteristics. Increased yield in said plants may be the result of, for example, improved plant physiology, growth and development, such as water use efficiency, water retention efficiency, improved nitrogen use, enhanced carbon assimilation, improved photosynthesis, increased germination efficiency and accelerated maturation. Yield may furthermore be affected by improved plant architecture (under stress and non-stress conditions), including but not limited to, early flowering, flowering control for hybrid seed production, seedling vigor, plant size, internode number and distance, root growth, seed size, fruit size, pod size, pod or ear number, seed number per pod or ear, seed mass, enhanced seed filling, reduced seed dispersal, reduced pod dehiscence and lodging resistance. Further yield traits include seed composition, such as carbohydrate content and composition for example cotton or starch, protein content, oil content and composition, nutritional value, reduction in anti-nutritional compounds, improved processability and better storage stability.

Plants and plant cultivars which may be treated by the above disclosed methods include plants and plant cultivars which are hybrid plants that already express the characteristic of heterosis or hybrid vigor which results in generally higher yield, vigor, health and resistance towards biotic and abiotic stresses.

Plants and plant cultivars (obtained by plant biotechnology methods such as genetic engineering) which may be treated by the above disclosed methods include plants and plant cultivars which are herbicide-tolerant plants, i.e. plants made tolerant to one or more given herbicides. Such plants can be obtained either by genetic transformation, or by selection of plants containing a mutation imparting such herbicide tolerance.

Plants and plant cultivars (obtained by plant biotechnology methods such as genetic engineering) which may be treated by the above disclosed methods include plants and plant cultivars which are insect-resistant transgenic plants, i.e. plants made resistant to attack by certain target insects. Such plants can be obtained by genetic transformation, or by selection of plants containing a mutation imparting such insect resistance.

Plants and plant cultivars (obtained by plant biotechnology methods such as genetic engineering) which may be treated by the above disclosed methods include plants and plant cultivars which are disease-resistant transgenic plants, i.e. plants made resistant to attack by certain target insects. Such plants can be obtained by genetic transformation, or by selection of plants containing a mutation imparting such insect resistance.

Plants and plant cultivars (obtained by plant biotechnology methods such as genetic engineering) which may be treated by the above disclosed methods include plants and plant cultivars which are tolerant to abiotic stresses. Such plants can be obtained by genetic transformation, or by selection of plants containing a mutation imparting such stress resistance.

Plants and plant cultivars (obtained by plant biotechnology methods such as genetic engineering) which may be treated by the above disclosed methods include plants and plant cultivars which show altered quantity, quality and/or storage-stability of the harvested product and/or altered properties of specific ingredients of the harvested product.

Plants and plant cultivars (obtained by plant biotechnology methods such as genetic engineering) which may be treated by the above disclosed methods include plants and plant cultivars, such as cotton plants, with altered fiber characteristics. Such plants can be obtained by genetic transformation, or by selection of plants contain a mutation imparting such altered fiber characteristics.

Plants and plant cultivars (obtained by plant biotechnology methods such as genetic engineering) which may be treated by the above disclosed methods include plants and plant cultivars, such as oilseed rape or related Brassica plants, with altered oil profile characteristics. Such plants can be obtained by genetic transformation, or by selection of plants contain a mutation imparting such altered oil profile characteristics.

Plants and plant cultivars (obtained by plant biotechnology methods such as genetic engineering) which may be treated by the above disclosed methods include plants and plant cultivars, such as oilseed rape or related Brassica plants, with altered seed shattering characteristics. Such plants can be obtained by genetic transformation, or by selection of plants contain a mutation imparting such altered seed shattering characteristics and include plants such as oilseed rape plants with delayed or reduced seed shattering.

Plants and plant cultivars (obtained by plant biotechnology methods such as genetic engineering) which may be treated by the above disclosed methods include plants and plant cultivars, such as Tobacco plants, with altered post-translational protein modification patterns.

Pathogens

Non-limiting examples of pathogens of fungal diseases which may be treated in accordance with the invention include:

diseases caused by powdery mildew pathogens, for example Blumeria species, for example Blumeria graminis; Podosphaera species, for example Podosphaera leucotricha; Sphaerotheca species, for example Sphaerotheca fuliginea; Uncinula species, for example Uncinula necator; diseases caused by rust disease pathogens, for example Gymnosporangium species, for example Gymnosporangium sabinae; Hemileia species, for example Hemileia vastatrix; Phakopsora species, for example Phakopsora pachyrhizi or Phakopsora meibomiae; Puccinia species, for example Puccinia recondita, Puccinia graminis oder Puccinia striiformis; Uromyces species, for example Uromyces appendiculatus; diseases caused by pathogens from the group of the Oomycetes, for example Albugo species, for example Albugo candida; Bremia species, for example Bremia lactucae; Peronospora species, for example Peronospora pisi or P. brassicae; Phytophthora species, for example Phytophthora infestans; Plasmopara species, for example Plasmopara viticola; Pseudoperonospora species, for example Pseudoperonospora humuli or Pseudoperonospora cubensis; Pythium species, for example Pythium ultimum; leaf blotch diseases and leaf wilt diseases caused, for example, by Alternaria species, for example Alternaria solani and Alternaria alternate; Cercospora species, for example Cercospora beticola; Cladiosporium species, for example Cladiosporium cucumerinum; Cochliobolus species, for example Cochliobolus sativus (conidial form: Drechslera, syn: Helminthosporium) or Cochliobolus miyabeanus; Colletotrichum species, for example Colletotrichum lindemuthanium; Cordana species, for example Cordana musae; Corynespora species, for example Corynespora cassiicola; Cycloconium species, for example Cycloconium oleaginum; Diaporthe species, for example Diaporthe citri; Elsinoe species, for example Elsinoe fawcettii; Gloeosporium species, for example Gloeosporium laeticolor; Glomerella species, for example Glomerella cingulata; Guignardia species, for example Guignardia bidwelli; Leptosphaeria species, for example Leptosphaeria maculans; Magnaporthe species, for example Magnaporthe grisea; Microdochium species, for example Microdochium nivale; Mycosphaerella species, for example Mycosphaerella graminicola, Mycosphaerella arachidicola or Mycosphaerella fijiensis; Parastagonospora species, for example Parastagonospora nodorum; Phaeosphaeria species, for example Phaeosphaeria nodorum; Pyrenophora species, for example Pyrenophora teres or Pyrenophora tritici repentis; Ramularia species, for example Ramularia collo-cygni or Ramularia areola; Rhynchosporium species, for example Rhynchosporium secalis; Septoria species, for example Septoria apii or Septoria lycopersici; Stagonospora species, for example Stagonospora nodorum; Typhula species, for example Typhula incarnata; Ustilago species, for example Ustilago segetum; Venturia species, for example Venturia inaequalis; root and stem diseases caused, for example, by Corticium species, for example Corticium graminearum; Fusarium species, for example Fusarium oxysporum; Gaeumannomyces species, for example Gaeumannomyces graminis; Plasmodiophora species, for example Plasmodiophora brassicae; Rhizoctonia species, for example Rhizoctonia solani; Sarocladium species, for example Sarocladium oryzae; Sclerotium species, for example Sclerotium oryzae; Tapesia species, for example Tapesia acuformis; Thielaviopsis species, for example Thielaviopsis basicola; ear and panicle diseases (including corn cobs) caused, for example, by Alternaria species, for example Alternaria spp.; Aspergillus species, for example Aspergillus flavus; Cladosporium species, for example Cladosporium cladosporioides; Claviceps species, for example Claviceps purpurea; Fusarium species, for example Fusarium culmorum; Gibberella species, for example Gibberella zeae; Monographella species, for example Monographella nivalis; Stagnospora species, for example Stagnospora nodorum; diseases caused by smut fungi, for example Sphacelotheca species, for example Sphacelotheca reiliana; Tilletia species, for example Tilletia caries or Tilletia controversa; Urocystis species, for example Urocystis occulta; Ustilago species, for example Ustilago nuda; fruit rot caused, for example, by Aspergillus species, for example Aspergillus flavus; Botrytis species, for example Botrytis cinerea; Monilinia species, for example Monilinia laxa; Penicillium species, for example Penicillium expansum or Penicillium purpurogenum; Rhizopus species, for example Rhizopus stolonifer; Sclerotinia species, for example Sclerotinia sclerotiorum; Verticilium species, for example Verticilium alboatrum; seed- and soil-borne rot and wilt diseases, and also diseases of seedlings, caused, for example, by Alternaria species, for example Alternaria brassicicola; Aphanomyces species, for example Aphanomyces euteiches; Ascochyta species, for example Ascochyta lentis; Aspergillus species, for example Aspergillus flavus; Cladosporium species, for example Cladosporium herbarum; Cochliobolus species, for example Cochliobolus sativus (conidial form: Drechslera, Bipolaris Syn: Helminthosporium); Colletotrichum species, for example Colletotrichum coccodes; Fusarium species, for example Fusarium culmorum; Gibberella species, for example Gibberella zeae; Macrophomina species, for example Macrophomina phaseolina; Microdochium species, for example Microdochium nivale; Monographella species, for example Monographella nivalis; Penicillium species, for example Penicillium expansum; Phoma species, for example Phoma lingam; Phomopsis species, for example Phomopsis sojae; Phytophthora species, for example Phytophthora cactorum; Pyrenophora species, for example Pyrenophora graminea; Pyricularia species, for example Pyricularia oryzae; Pythium species, for example Pythium ultimum; Rhizoctonia species, for example Rhizoctonia solani; Rhizopus species, for example Rhizopus oryzae; Sclerotium species, for example Sclerotium rolfsii; Septoria species, for example Septoria nodorum; Typhula species, for example Typhula incarnata; Verticillium species, for example Verticillium dahliae; cancers, galls and witches' broom caused, for example, by Nectria species, for example Nectria galligena; wilt diseases caused, for example, by Verticillium species, for example Verticillium longisporum; Fusarium species, for example Fusarium oxysporum; deformations of leaves, flowers and fruits caused, for example, by Exobasidium species, for example Exobasidium vexans; Taphrina species, for example Taphrina deformans; degenerative diseases in woody plants, caused, for example, by Esca species, for example Phaeomoniella chlamydospora, Phaeoacremonium aleophilum or Fomitiporia mediterranea; Ganoderma species, for example Ganoderma boninense; diseases of plant tubers caused, for example, by Rhizoctonia species, for example Rhizoctonia solani; Helminthosporium species, for example Helminthosporium solani; diseases caused by bacterial pathogens, for example Xanthomonas species, for example Xanthomonas campestris pv. oryzae; Pseudomonas species, for example Pseudomonas syringae pv. lachrymans; Erwinia species, for example Erwinia amylovora; Liberibacter species, for example Liberibacter asiaticus; Xyella species, for example Xylella fastidiosa; Ralstonia species, for example Ralstonia solanacearum; Dickeya species, for example Dickeya solani; Clavibacter species, for example Clavibacter michiganensis; Streptomyces species, for example Streptomyces scabies. diseases of soya beans: Fungal diseases on leaves, stems, pods and seeds caused, for example, by Alternaria leaf spot (Alternaria spec. atrans tenuissima), Anthracnose (Colletotrichum gloeosporoides dematium var. truncatum), brown spot (Septoria glycines), cercospora leaf spot and blight (Cercospora kikuchii), choanephora leaf blight (Choanephora infundibulifera trispora (Syn.)), dactuliophora leaf spot (Dactuliophora glycines), downy mildew (Peronospora manshurica), drechslera blight (Drechslera glycini), frogeye leaf spot (Cercospora sojina), leptosphaerulina leaf spot (Leptosphaerulina trifolii), phyllostica leaf spot (Phyllosticta sojaecola), pod and stem blight (Phomopsis sojae), powdery mildew (Microsphaera diffusa), pyrenochaeta leaf spot (Pyrenochaeta glycines), rhizoctonia aerial, foliage, and web blight (Rhizoctonia solani), rust (Phakopsora pachyrhizi, Phakopsora meibomiae), scab (Sphaceloma glycines), stemphylium leaf blight (Stemphylium botryosum), sudden death syndrome (Fusarium virguliforme), target spot (Corynespora cassiicola).

Fungal diseases on roots and the stem base caused, for example, by black root rot (Calonectria crotalariae), charcoal rot (Macrophomina phaseolina), fusarium blight or wilt, root rot, and pod and collar rot (Fusarium oxysporum, Fusarium orthoceras, Fusarium semitectum, Fusarium eauiseti), mycoleptodiscus root rot (Mycoleptodiscus terrestris), neocosmospora (Neocosmospora vasinfecta), pod and stem blight (Diaporthe phaseolorum), stem canker (Diaporthe phaseolorum var. caulivora), phytophthora rot (Phytophthora megasperma), brown stem rot (Phialophora gregata), pythium rot (Pythium aphanidermatum, Pythium irregulare, Pythium debaryanum, Pythium myriotylum, Pythium ultimum), rhizoctonia root rot, stem decay, and damping-off (Rhizoctonia solani), sclerotinia stem decay (Sclerotinia sclerotiorum), sclerotinia southern blight (Sclerotinia rolfsii), thielaviopsis root rot (Thielaviopsis basicola).

Mycotoxins

In addition, the compound combination and the composition of the invention may reduce the mycotoxin content in the harvested material and the foods and feeds prepared therefrom. Mycotoxins include particularly, but not exclusively, the following: deoxynivalenol (DON), nivalenol, 15-Ac-DON, 3-Ac-DON, T2- and HT2-toxin, fumonisins, zearalenon, moniliformin, fusarin, diaceotoxyscirpenol (DAS), beauvericin, enniatin, fusaroproliferin, fusarenol, ochratoxins, patulin, ergot alkaloids and aflatoxins which can be produced, for example, by the following fungi: Fusarium spec., such as F. acuminatum, F. asiaticum, F. avenaceum, F. crookwellense, F. culmorum, F. graminearum (Gibberella zeae), F. equiseti, F. fujikoroi, F. musarum, F. oxysporum, F. proliferatum, F. poae, F. pseudograminearum, F. sambucinum, F. scirpi, F. semitectum, F. solani, F. sporotrichoides, F. langsethiae, F. subglutinans, F. tricinctum, F. verticillioides, and also by Aspergillus spec., such as A. flavus, A. parasiticus, A. nomius, A. ochraceus, A. clavatus, A. terreus, A. versicolor, Penicillium spec., such as P. verrucosum, P. viridicatum, P. citrinum, P. expansum, P. claviforme, P. roqueforti, Claviceps spec., such as C. purpurea, C. fusiformis, C. paspali, C. africana, Stachybotrys spec. and others.

Material Protection

The compound combination and the composition of the invention may also be used in the protection of materials, especially for the protection of industrial materials against attack and destruction by phytopathogenic fungi.

In addition, the compound combination and the composition of the invention may be used as antifouling compositions, alone or in combinations with other active ingredients.

Industrial materials in the present context are understood to mean inanimate materials which have been prepared for use in industry. For example, industrial materials which are to be protected from microbial alteration or destruction may be adhesives, glues, paper, wallpaper and board/cardboard, textiles, carpets, leather, wood, fibers and tissues, paints and plastic articles, cooling lubricants and other materials which can be infected with or destroyed by microorganisms. Parts of production plants and buildings, for example cooling-water circuits, cooling and heating systems and ventilation and air-conditioning units, which may be impaired by the proliferation of microorganisms may also be mentioned within the scope of the materials to be protected. Industrial materials within the scope of the present invention preferably include adhesives, sizes, paper and card, leather, wood, paints, cooling lubricants and heat transfer fluids, more preferably wood.

The compound combination and the composition of the invention may prevent adverse effects, such as rotting, decay, discoloration, decoloration or formation of mould.

In the case of treatment of wood the compound combination and the composition of the invention may also be used against fungal diseases liable to grow on or inside timber.

Timber means all types of species of wood, and all types of working of this wood intended for construction, for example solid wood, high-density wood, laminated wood, and plywood. In addition, the compound and the composition of the invention may be used to protect objects which come into contact with saltwater or brackish water, especially hulls, screens, nets, buildings, moorings and signalling systems, from fouling.

The compound combination and the composition of the invention may also be employed for protecting storage goods. Storage goods are understood to mean natural substances of vegetable or animal origin or processed products thereof which are of natural origin, and for which long-term protection is desired. Storage goods of vegetable origin, for example plants or plant parts, such as stems, leaves, tubers, seeds, fruits, grains, may be protected freshly harvested or after processing by (pre)drying, moistening, comminuting, grinding, pressing or roasting. Storage goods also include timber, both unprocessed, such as construction timber, electricity poles and barriers, or in the form of finished products, such as furniture. Storage goods of animal origin are, for example, hides, leather, furs and hairs. The compound combination and the composition of the invention may prevent adverse effects, such as rotting, decay, discoloration, decoloration or formation of mould.

Microorganisms capable of degrading or altering industrial materials include, for example, bacteria, fungi, yeasts, algae and slime organisms. The compound combination and the composition of the invention preferably act against fungi, especially moulds, wood-discoloring and wood-destroying fungi (Ascomycetes, Basidiomycetes, Deuteromycetes and Zygomycetes), and against slime organisms and algae. Examples include microorganisms of the following genera: Alternaria, such as Alternaria tenuis; Aspergillus, such as Aspergillus niger; Chaetomium, such as Chaetomium globosum; Coniophora, such as Coniophora puetana; Lentinus, such as Lentinus tigrinus; Penicillium, such as Penicillium glaucum; Polyporus, such as Polyporus versicolor; Aureobasidium, such as Aureobasidium pullulans; Sclerophoma, such as Sclerophoma pityophila; Trichoderma, such as Trichoderma viride; Ophiostoma spp., Ceratocystis spp., Humicola spp., Petriella spp., Trichurus spp., Coriolus spp., Gloeophyllum spp., Pleurotus spp., Poria spp., Serpula spp. and Tyromyces spp., Cladosporium spp., Paecilomyces spp. Mucor spp., Escherichia, such as Escherichia coli; Pseudomonas, such as Pseudomonas aeruginosa; Staphylococcus, such as Staphylococcus aureus, Candida spp. and Saccharomyces spp., such as Saccharomyces cerevisae.

Seed Treatment

The compound combination and the composition of the invention may also be used to protect seeds from unwanted microorganisms, such as phytopathogenic microorganisms, for instance phytopathogenic fungi or phytopathogenic oomycetes. The term seed(s) as used herein include dormant seeds, primed seeds, pregerminated seeds and seeds with emerged roots and leaves.

Thus, the present invention also relates to a method for protecting seeds from unwanted microorganisms which comprises the step of treating the seeds with the compound combination or the composition of the invention, wherein the seeds may be treated simultaneously, separately or sequentially with the compounds (A) and (B).

The treatment of seeds with the compound combination or the composition of the invention protects the seeds from phytopathogenic microorganisms, but also protects the germinating seeds, the emerging seedlings and the plants after emergence from the treated seeds. Therefore, the present invention also relates to a method for protecting seeds, germinating seeds and emerging seedlings.

The seeds treatment may be performed prior to sowing, at the time of sowing or shortly thereafter.

When the seeds treatment is performed prior to sowing (e.g. so-called on-seed applications), the seeds treatment may be performed as follows: the seeds may be placed into a mixer with a desired amount of the compound combination or the composition of the invention, the seeds and the compound combination or the composition of the invention are mixed until an homogeneous distribution on seeds is achieved. If appropriate, the seeds may then be dried.

The invention also relates to seeds coated with the compound combination or the composition of the invention.

Preferably, the seeds are treated in a state in which it is sufficiently stable for no damage to occur in the course of treatment. In general, seeds can be treated at any time between harvest and shortly after sowing. It is customary to use seeds which have been separated from the plant and freed from cobs, shells, stalks, coats, hairs or the flesh of the fruits. For example, it is possible to use seeds which have been harvested, cleaned and dried down to a moisture content of less than 15% by weight. Alternatively, it is also possible to use seeds which, after drying, for example, have been treated with water and then dried again, or seeds just after priming, or seeds stored in primed conditions or pre-germinated seeds, or seeds sown on nursery trays, tapes or paper.

The amount of the compound combination or the composition of the invention applied to the seeds is typically such that the germination of the seed is not impaired, or that the resulting plant is not damaged. This must be ensured particularly in case the compounds contained in the compound combination of the invention would exhibit phytotoxic effects at certain application rates. The intrinsic phenotypes of transgenic plants should also be taken into consideration when determining the amount of the compound combination of the invention to be applied to the seed in order to achieve optimum seed and germinating plant protection with a minimum amount of compound being employed.

The compounds contained in the compound combination of the invention can be applied as such, directly to the seeds, i.e. without the use of any other components and without having been diluted. They can be applied in a simultaneous, separate or sequential manner. Also compositions containing the compounds contained in the compound combination of the invention, such as the composition of the invention, can be applied to the seeds.

The compound combination and the composition of the invention are suitable for protecting seeds of any plant variety. Preferred seeds are that of cereals (such as wheat, barley, rye, millet, triticale, and oats), oilseed rape, maize, cotton, soybean, rice, potatoes, sunflower, beans, coffee, peas, beet (e.g. sugar beet and fodder beet), peanut, vegetables (such as tomato, cucumber, onions and lettuce), lawns and ornamental plants. More preferred are seeds of wheat, soybean, oilseed rape, maize and rice.

The compound combination and the composition of the invention may be used for treating transgenic seeds, in particular seeds of plants capable of expressing a polypeptide or protein which acts against pests, herbicidal damage or abiotic stress, thereby increasing the protective effect. Seeds of plants capable of expressing a polypeptide or protein which acts against pests, herbicidal damage or abiotic stress may contain at least one heterologous gene which allows the expression of said polypeptide or protein. These heterologous genes in transgenic seeds may originate, for example, from microorganisms of the species Bacillus, Rhizobium, Pseudomonas, Serratia, Trichoderma, Clavibacter, Glomus or Gliocladium. These heterologous genes preferably originate from Bacillus sp., in which case the gene product is effective against the European corn borer and/or the Western corn rootworm. Particularly preferably, the heterologous genes originate from Bacillus thuringiensis.

Application

The compound combination of the invention can be applied as such, or for example in the form of as ready-to-use solutions, emulsions, water- or oil-based suspensions, powders, wettable powders, pastes, soluble powders, dusts, soluble granules, granules for broadcasting, suspoemulsion concentrates, natural products impregnated with the compound combination of the invention, synthetic substances impregnated with the compound combination of the invention, fertilizers or microencapsulations in polymeric substances.

Application is accomplished in a customary manner, for example by watering, spraying, atomizing, broadcasting, dusting, foaming or spreading-on. It is also possible to deploy the compound combination of the invention by the ultra-low volume method, via a drip irrigation system or drench application, to apply it in-furrow or to inject it into the soil stem or trunk. It is further possible to apply the compound combination of the invention by means of a wound seal, paint or other wound dressing. The effective and plant-compatible amount of the compound combination of the invention which is applied to the plants, plant parts, fruits, seeds or soil will depend on various factors, such as the compound/composition employed, the subject of the treatment (plant, plant part, fruit, seed or soil), the type of treatment (dusting, spraying, seed dressing), the purpose of the treatment (curative and protective), the type of microorganisms, the development stage of the microorganisms, the sensitivity of the microorganisms, the crop growth stage and the environmental conditions.

When the compound combination of the invention is used as a fungicide, the application rates can vary within a relatively wide range, depending on the kind of application. For the treatment of plant parts, such as leaves, the application rate may range from 0.1 to 10 000 g/ha, preferably from 10 to 1000 g/ha, more preferably from 50 to 300 g/ha (in the case of application by watering or dripping, it is even possible to reduce the application rate, especially when inert substrates such as rockwool or perlite are used). For the treatment of seeds, the application rate may range from 0.1 to 200 g per 100 kg of seeds, preferably from 1 to 150 g per 100 kg of seeds, more preferably from 2.5 to 25 g per 100 kg of seeds, even more preferably from 2.5 to 12.5 g per 100 kg of seeds. For the treatment of soil, the application rate may range from 0.1 to 10 000 g/ha, preferably from 1 to 5000 g/ha. The outlined application rates refer to the total application rates of compounds (A) and (B) present in the compound combination of the present invention.

These application rates are merely examples and are not intended to limit the scope of the present invention.

The compound combination of the invention can be used in combination with models e.g. embedded in computer programs for site specific crop management, satellite farming, precision farming or precision agriculture. Such models support the site specific management of agricultural sites with data from various sources such as soils, weather, crops (e.g. type, growth stage, plant health), weeds (e.g. type, growth stage), diseases, pests, nutrients, water, moisture, biomass, satellite data, yield etc. with the purpose to optimize profitability, sustainability and protection of the environment. In particular, such models can help to optimize agronomical decisions, control the precision of pesticide applications and record the work performed.

As an example, the compound of the invention can be applied to a crop plant according to appropriate dose regime if a model models the development of a fungal disease and calculates that a threshold has been reached for which it is recommendable to apply the compound of the invention to the crop plant.

Commercially available systems which include agronomic models are e.g. FieldScripts™ from The Climate Corporation, Xarvio™ from BASF, AGLogic™ from John Deere, etc.

The compounds of the invention can also be used in combination with smart spraying equipment such as e.g. spot spraying or precision spraying equipment attached to or housed within a farm vehicle such as a tractor, robot, helicopter, airplane, unmanned aerial vehicle (UAV) such as a drone, etc. Such an equipment usually includes input sensors (such as e.g. a camera) and a processing unit configured to analyze the input data and configured to provide a decision based on the analysis of the input data to apply the compound of the invention to the crop plants (respectively the weeds) in a specific and precise manner. The use of such smart spraying equipment usually also requires positions systems (e.g. GPS receivers) to localize recorded data and to guide or to control farm vehicles; geographic information systems (GIS) to represent the information on intelligible maps, and appropriate farm vehicles to perform the required farm action such as the spraying.

In an example, fungal diseases can be detected from imagery acquired by a camera. In an example fungal diseases can be identified and/or classified based on that imagery. Such identification and/classification can make use of image processing algorithms. Such image processing algorithms can utilize machine learning algorithms, such as trained neutral networks, decision trees and utilize artificial intelligence algorithms. In this manner, the compounds described herein can be applied only where needed.

EXAMPLES

Generality

Measurement of Log P values

Measurement of Log P values as provided herein was performed according to EEC directive 79/831 Annex V.A8 by HPLC (High Performance Liquid Chromatography) on reversed phase columns with the following methods:

-   -   ^([a]) Log P value is determined by measurement of LC-UV, in an         acidic range, with 0.1% formic acid in water and acetonitrile as         eluent (linear gradient from 10% acetonitrile to 95%         acetonitrile).     -   ^([b]) Log P value is determined by measurement of LC-UV, in a         neutral range, with 0.001 molar ammonium acetate solution in         water and acetonitrile as eluent (linear gradient from 10%         acetonitrile to 95% acetonitrile).     -   ^([c]) Log P value is determined by measurement of LC-UV, in an         acidic range, with 0.1% phosphoric acid and acetonitrile as         eluent (linear gradient from 10% acetonitrile to 95%         acetonitrile).

If more than one Log P value is available within the same method, all the values are given and separated by “+”.

Calibration was done with straight-chain alkan2-ones (with 3 to 16 carbon atoms) with known Log P values (measurement of Log P values using retention times with linear interpolation between successive alkanones). Lambda-max-values were determined using UV-spectra from 200 nm to 400 nm and the peak values of the chromatographic signals

¹H-NMR Data

¹H-NMR data of selected examples as provided herein are written in form of 1H-NMR-peak lists. To each signal peak are listed the δ-value in ppm and the signal intensity in round brackets. Between the δ-value —signal intensity pairs are semicolons as delimiters.

The peak list of an example has therefore the form:

δ₁ (intensity₁); δ₂ (intensity₂); . . . ; δ_(i) (intensity_(i)); . . . ; δ_(n) (intensity_(n))

Intensity of sharp signals correlates with the height of the signals in a printed example of a NMR spectrum in cm and shows the real relations of signal intensities. From broad signals several peaks or the middle of the signal and their relative intensity in comparison to the most intensive signal in the spectrum can be shown. For calibrating chemical shift for 1H spectra, we use tetramethylsilane and/or the chemical shift of the solvent used, especially in the case of spectra measured in DMSO. Therefore in NMR peak lists, tetramethylsilane peak can occur but not necessarily.

The 1H-NMR peak lists are similar to classical 1H-NMR prints and contains therefore usually all peaks, which are listed at classical NMR-interpretation.

Additionally they can show like classical 1H-NMR prints signals of solvents, stereoisomers of the target compounds, which are also object of the invention, and/or peaks of impurities.

To show compound signals in the delta-range of solvents and/or water the usual peaks of solvents, for example peaks of DMSO in DMSO-D₆ and the peak of water are shown in our 1H-NMR peak lists and have usually on average a high intensity.

The peaks of stereoisomers of the target compounds and/or peaks of impurities have usually on average a lower intensity than the peaks of target compounds (for example with a purity >90%).

Such stereoisomers and/or impurities can be typical for the specific preparation process. Therefore their peaks can help to recognize the reproduction of our preparation process via “side-products-fingerprints”.

An expert, who calculates the peaks of the target compounds with known methods (MestreC, ACD-simulation, but also with empirically evaluated expectation values) can isolate the peaks of the target compounds as needed optionally using additional intensity filters. This isolation would be similar to relevant peak picking at classical 1H-NMR interpretation.

Further details of NMR-data description with peak lists you find in the publication “Citation of NMR Peaklist Data within Patent Applications” of the Research Disclosure Database Number 564025.

Separation of Enantiomers

Enantiomeric separations of racemates are performed by preparative supercritical fluid chromatography using supercritical carbon dioxide as mobile phase and lower alcohols as modifier, more preferably methanol, ethanol or isopropanol in a ratio comprised between 15 and 30% by volume. Total flow rates are in a range 70-100 ml/min and chromatographic separations are done at a temperature in a range of between 30° C. and 50° C. and a back pressure in a range of between 70 bar to 130 bar on one of the thermostated chiral stationary phases, commercially available and known as follows:

-   -   ChiralPak® IA, 250×20 mm from Daicel Chemical Industries, Ltd.     -   Lux® Amylose-1, 250×21.2 mm 5 μm, Axia packed from Phenomenex         Inc.     -   Lux® Cellulose-1, 250×21.2 mm 5 μm, Axia packed from Phenomenex         Inc.     -   Lux® i-Cellulose-5, 250×21.2 mm 5 μm, Axia packed from         Phenomenex Inc.

The separations on preparative scale were performed on apparatus SFC-PICLAB Hybrid 10-150 from Pic Solution with UV-detection in a range of between 210 nm and 280 nm, preferably 220 and 254 nm.

The following examples illustrate in a non-limiting manner the preparation and biological activity of the compounds of formula (I) according to the invention.

Synthesis of Compounds of Formula (I) and Intermediates

Synthesis of Compounds of Formula (I)

Preparation of Example 1: Preparation of rac-3-[6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazin-4-yl]-5-[(2,4-dimethylphenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazine (Compound 1.059) Step 1: Preparation of ethyl 6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboxylate

Under argon, sodium hydride (2.8 g, 70 mmol) was added to a solution of 3-(trifluoromethyl)phenol (9.7 g, 60 mmol) in DMF (30 mL). The reaction mixture was stirred 1 h at room temperature, then ethyl 3,6-dichloropyridazine-4-carboxylate (13.8 g, 50 mmol) was added portionwise to the solution. The reaction mixture was stirred for 18 h at room temperature, then diluted with water and extracted with ether (3×200 mL). The organic extracts were washed with water and brine, dried over magnesium sulfate, filtered and concentrated under reduced pressure. Purification of the residue by column chromatography on silica gel (gradient heptane/EtOAc) afforded, after evaporation of the solvents, 20 g (90% purity, 100% yield) of ethyl 6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboxylate as an oil.

Step 2: Preparation of 6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboxylic acid

To a solution of ethyl 6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboxylate (15 g, 35 mmol) in dioxane/water 2:1 (75 mL) was added lithium hydroxide (2.5 g, 105 mmol). The reaction was stirred for 4 h at room temperature then diluted with water. The aqueous phase was acidified with 1M aqueous HCl solution and extracted with ethyl acetate (3×200 mL). The organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure. Evaporation of the solvents afforded 9.7 g (98% purity, 85% yield) of 6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboxylic acid as a solid.

Step 3: Preparation of 6-chloro-N-[rac-1-[(2,4-dimethylphenyl)methyl]-2-(1,3-dioxoisoindolin-2-yl)oxy-ethyl]-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboxamide (Compound 3-16)

Under argon, to a solution of 6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboxylic acid (5.0 g, 15.7 mmol) and HATU (6.56 g, 17.26 mmol) in DMF (100 mL) were successively added at 0° C., 2-[rac-2-amino-3-(2,4-dimethylphenyl)propoxy]isoindoline-1,3-dione; 2,2,2-trifluoroacetic acid (7.57 g, 17.26 mmol) and N,N-Diisopropylethylamine (8.2 mL, 47.07 mmol). After 15 min at 0° C., the reaction mixture was stirred for 3 h at room temperature. It was then diluted with water and extracted with ethyl acetate (2×200 mL). The organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure. Purification of the residue by column chromatography on silica gel (gradient heptane/EtOAc) afforded, after evaporation of the solvents, 7.95 g (100% purity, 81% yield) of 6-chloro-N-[rac-1-[(2,4-dimethylphenyl)methyl]-2-(1,3-dioxoisoindolin-2-yl)oxy-ethyl]-3-[3-(trifluoro-methyl)phenoxy]pyridazine-4-carboxamide as a white solid.

Step 4: Preparation of 6-chloro-N-[rac-1-(aminooxymethyl)-2-(2,4-dimethylphenyl)ethyl]-3-[3-(trifluoro-methyl)phenoxy]pyridazine-4-carboxamide (Compound 4-17)

Under argon, hydrazine monohydrate (2.31 mL, 37.92 mmol) was added to a solution of 6-chloro-N-[rac-1-[(2,4-dimethylphenyl)methyl]-2-(1,3-dioxoisoindolin-2-yl)oxy-ethyl]-3-[3-(trifluoro-methyl)phenoxy]pyridazine-4-carboxamide (7.9 g, 12.64 mmol) in DCM/MeOH (110 mL, 1:1). The reaction mixture was stirred for 4 h at room temperature and concentrated. It was then diluted with water and extracted with ethyl acetate (2×200 mL). The organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure. Evaporation of the solvents afforded 6.35 g (97% purity, 98% yield) of 6-chloro-N-[rac-1-(aminooxymethyl)-2-(2,4-dimethylphenyl)ethyl]-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboxamide as a yellow oil.

Step 5: Preparation of rac-3-[6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazin-4-yl]-5-[(2,4-dimethyl-phenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazine

Under argon, POCl₃ (3.56 mL, 38.19 mmol) was added at 80° C. to a solution 6-chloro-N-[rac-1-(aminooxymethyl)-2-(2,4-dimethylphenyl)ethyl]-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboxamide (6.3 g, 12.73 mmol) in AcCN (114 mL). The reaction mixture was stirred for 18 h at 80° C. After cooling to room temperature, the mixture was poured into a saturated sodium bicarbonate solution, then extracted with ethyl acetate (2×200 mL). The organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure. Purification of the residue by column chromatography on silica gel (gradient heptane/EtOAc) afforded, after evaporation of the solvents, 2.52 g (98% purity, 41% yield) of rac-3-[6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazin-4-yl]-5-[(2,4-dimethylphenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazine as a yellow solid.

Preparation of Example 2: Preparation of rac-3-[6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazin-4-yl]-5-[(2,4-dimethylphenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazine (Compound 1.059) Step 1: Preparation of 6-chloro-N-[1-(chloromethyl)-2-(2,4-dimethylphenyl)ethyl]-3-[3-(trifluoro-methyl)phenoxy]pyridazine-4-carboxamide (Compound 21-01)

To a solution of 6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboxylic acid (100 mg, 0.31 mmol) in dichloromethane (2 mL) was added at room temperature oxalyl chloride (119 mg, 0.94 mmol) and a drop of dimethylformamide. After 30 min, the reaction was concentrated under reduced pressure. The residue was dissolved in dichloromethane (2 ml) and added at 0° C. to a suspension of 1-chloro-3-(2,4-dimethylphenyl)propan-2-amine; hydrochloride (73 mg, 0.31 mmol) in dichloromethane (1 mL), followed by addition of N,N-diisopropylethylamine (0.16 mL, 0.94 mmol). The reaction mixture was stirred at room temperature for 1 h, then concentrated under reduced pressure. Purification of the residue by column chromatography on silica gel (gradient heptane/EtOAc) afforded, after evaporation of the solvents, 142 mg (87% purity, 79% yield) of 6-chloro-N-[1-(chloromethyl)-2-(2,4-dimethylphenyl)ethyl]-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboxamide as a colourless oil.

Step 2: Preparation of 6-chloro-N-[1-(chloromethyl)-2-(2,4-dimethylphenyl)ethyl]-N′-hydroxy-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboxamidine (Compound 20-01)

To a solution of 6-chloro-N-[1-(chloromethyl)-2-(2,4-dimethylphenyl)ethyl]-3-[3-(trifluoro-methyl)phenoxy]pyridazine-4-carboxamide (130 mg, 0.23 mmol) in AcCN (2 mL) was added phosphorous pentachloride (205 mg, 0.99 mmol). The reaction mixture was stirred at room temperature for 18 h, then concentrated under reduced pressure. The residue was dissolved in AcCN (5 mL) and a solution of hydroxylamine in water (300 mg, 4.53 mmol, 50% in water) was added to the reaction mixture. After stirring at room temperature for 1 h the reaction mixture was diluted with water and toluene, and extracted with ethyl acetate (3×50 mL). The organic extracts were washed with water and brine, dried over sodium sulfate, filtered and concentrated under reduced pressure. Evaporation of the solvents, afforded 150 mg (65% purity, 83% yield) of 6-chloro-N-[1-(chloromethyl)-2-(2,4-dimethylphenyl)ethyl]-N′-hydroxy-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboxamidine as a yellow oil.

Step 3: Preparation of rac-3-[6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazin-4-yl]-5-[(2,4-dimethyl-phenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazine

To a solution of 6-chloro-N-[1-(chloromethyl)-2-(2,4-dimethylphenyl)ethyl]-N′-hydroxy-3-[3-(trifluoro-methyl)phenoxy]pyridazine-4-carboxamidine (150 mg, 0.23 mmol) in AcCN (2 mL) was added potassium tert-butoxide (47.3 mg, 0.42 mmol). The reaction mixture was stirred at room temperature for 1 h30, then diluted with a saturated ammonium chloride solution and extracted with dichloromethane (2×50 mL). The organic extracts were dried over sodium sulfate, filtered and concentrated under reduced pressure. Purification of the residue by column chromatography on silica gel (gradient heptane/EtOAc) afforded, after evaporation of the solvents, 56 mg (87% purity, 43% yield) of rac-3-[6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazin-4-yl]-5-[(2,4-dimethylphenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazine as a yellow solid.

Preparation of Example 3: Preparation of rac-5-(4-chlorophenyl)-3-[6-methyl-3-[3-(trifluoro-methyl)phenoxy]pyridazin-4-yl]-5,6-dihydro-4H-1,2,4-oxadiazine (Compound 1.040) Step 1: Preparation of 6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carbonitrile (Compound 9-03)

Under argon, sodium hydride (1.30 g, 32 mmol) was added at 0° C. to a solution of 3-(trifluoromethyl)phenol (4.6 g, 28 mmol) in THF (100 mL). After 30 min, 3,6-dichloropyridazine-4-carbonitrile (5.0 g, 28.7 mmol) was added portionwise to the solution. The reaction mixture was stirred for 3 h at room temperature, then diluted with saturated ammonium chloride solution and extracted with EtOAc (3×200 mL). The organic extracts were washed with water and brine, dried over magnesium sulfate, filtered and concentrated under reduced pressure. Purification of the residue by column chromatography on silica gel (gradient heptane/EtOAc) afforded, after evaporation of the solvents, 6.1 g (95% purity, 67% yield) of 6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carbonitrile as an oil.

Step 2: Preparation of 6-methyl-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carbonitrile (Compound 9-02)

Under argon, 2,4,6-trimethyl-1,3,5,2,4,6-trioxatriborinane (12.57 g, 50.0 mmol) was added to a stirred solution of 6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carbonitrile (3.0 g, 10.0 mmol), [1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium(II) complex with dichloromethane (64 mg, 0.10 mmol) and cesium carbonate (4.89 g, 15.0 mmol) in dioxane (30 mL). The reaction mixture was stirred at 100° C. for 4 h, then diluted with water and extracted with ethyl acetate (2×200 mL). The organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure. Purification of the residue by column chromatography on silica gel (gradient heptane/EtOAc) afforded, after evaporation of the solvents, 1.82 g (100% purity, 65% yield) of 6-methyl-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carbonitrile as a solid.

Step 3: preparation of N′-hydroxy-6-methyl-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboxamidine (Compound 10-02)

To a solution of 6-methyl-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carbonitrile (1.82 g, 6.52 mmol) in EtOH (32 mL) was added hydroxylamine hydrochloride (1.13 g, 16.29 mmol) and potassium carbonate (2.25 g, 16.29 mmol). The reaction mixture was stirred at 60° C. for 2 h. The precipitate was filtered off. The filtrate was concentrated, diluted with water and extracted with EtOAc (2×100 mL). The organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure. Purification of the residue by column chromatography on silica gel (gradient heptane/EtOAc) afforded, after evaporation of the solvents, 1.38 g (91% purity, 62% yield) of N′-hydroxy-6-methyl-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboxamidine as a yellow solid.

Step 4: preparation of N′-[2-(4-chlorophenyl)-2-oxo-ethoxy]-6-methyl-3-[3-(trifluoro-methyl)phenoxy]pyridazine-4-carboxamidine (Compound 12-03)

Under argon, 2-tert-butylimino-N,N-diethyl-1,3-dimethyl-1,3,2lambda5-diazaphosphinan-2-amine (BEMP) (210.9 mg, 0.77 mmol) was added at room temperature to a solution of N′-hydroxy-6-methyl-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboxamidine (200 mg, 0.64 mmol) in AcCN (2.7 mL). After 15 min, 2-bromo-1-(4-chlorophenyl)ethanone (224 mg, 0.96 mmol) was added, the reaction was stirred further for 3 h, then concentrated under reduced pressure. Purification of the residue by column chromatography on silica gel (gradient heptane/EtOAc) afforded, after evaporation of the solvents, 65.6 mg (91% purity, 20% yield) of N′-[2-(4-chlorophenyl)-2-oxo-ethoxy]-6-methyl-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboxamidine as an oil.

Step 5: Preparation of rac-5-(4-chlorophenyl)-3-[6-methyl-3-[3-(trifluoromethyl)phenoxy]pyridazin-4-yl]-5,6-dihydro-4H-1,2,4-oxadiazine

Under argon, N′-[2-(4-chlorophenyl)-2-oxo-ethoxy]-6-methyl-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboxamidine (69.2 mg, 0.13 mmol) was dissolved in MeOH (0.94 mL) and acetic acid (0.21 mL) and heated to 60° C. After 1 h, sodium cyanoborohydride (9.3 mg, 0.15 mmol) was added and the reaction was stirred further for 2 h. After cooling to room temperature, the mixture was poured into a 1M NaOH solution and extracted with ethyl acetate (2×20 mL). The organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure. Purification of the residue by PREP-HPLC afforded, after evaporation of the solvents, 29 mg (100% purity, 47% yield) of rac-5-(4-chlorophenyl)-3-[6-methyl-3-[3-(trifluoromethyl)phenoxy]pyridazin-4-yl]-5,6-dihydro-4H-1,2,4-oxadiazine as a solid.

Preparation of Example 4: Preparation of rac-5-(1-methylindol-3-yl)-3-[6-methyl-3-[3-(trifluoro-methyl)phenoxy]pyridazin-4-yl]-5,6-dihydro-4H-1,2,4-oxadiazine (Compound 1.011) Step 1: preparation of N′-allyloxy-6-methyl-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboxamidine (Compound 13-01)

Under argon, O-allylhydroxylamine hydrochloride (658 mg, 5.4 mmol) was added at room temperature to a stirred solution of 6-methyl-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carbonitrile (500 mg, 1.79 mol) and NaHCO₃ (752.1 mg, 8.95 mmol) in MeOH. The resulting mixture was stirred at 60° C. for 36 h, cooled to room temperature and concentrated under vacuum. The resulting mixture was extracted with dichloromethane (3×200 mL). The organic extracts were washed with brine, dried over sodium sulfate, filtered and concentrated under reduced pressure. Purification of the residue by column chromatography on silica gel (gradient PE/EtOAc) afforded, after evaporation of the solvents, 400 mg (98% purity, 63% yield) of N′-allyloxy-6-methyl-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboxamidine as a brown oil.

Step 2: Preparation of rac-3-[6-methyl-3-[3-(trifluoromethyl)phenoxy]pyridazin-4-yl]-5,6-dihydro-4H-1,2,4-oxadiazin-5-ol (Compound 14-01)

In a 50 mL round bottom flask OSO₄ (902 mg, 0.14 mmol, 4% wt in water) and NaIO₄ (759 mg, 3.55 mmol) were added at room temperature to a solution of N′-allyloxy-6-methyl-3-[3-(trifluoro-methyl)phenoxy]pyridazine-4-carboxamidine (500 mg, 1.42 mmol) in THF (20 ml) and water (5 mL). The reaction mixture was stirred for 2 h at room temperature, then diluted with a saturated ammonium chloride solution and extracted with ethyl acetate (2×100 mL). The organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure. Purification of the residue by column chromatography on silica gel (gradient heptane/EtOAc) afforded, after evaporation of the solvents, 260 mg (100% purity, 51% yield) of rac-3-[6-methyl-3-[3-(trifluoromethyl)phenoxy]pyridazin-4-yl]-5,6-dihydro-4H-1,2,4-oxadiazin-5-ol as a white solid.

Step 3: Preparation of rac-5-(1-methylindol-3-yl)-3-[6-methyl-3-[3-(trifluoromethyl)phenoxy]pyridazin-4-yl]-5,6-dihydro-4H-1,2,4-oxadiazine

In a 50 mL round bottom flask, 1-methylindole (37 mg, 0.28 mmol) was added to a solution of rac-3-[6-methyl-3-[3-(trifluoromethyl)phenoxy]pyridazin-4-yl]-5,6-dihydro-4H-1,2,4-oxadiazin-5-ol (50 mg, 0.14 mmol) in formic acid (2 mL). The reaction mixture was stirred for 45 min at 50° C. then cooled to room temperature and stirred further for 3 h. The solvent was removed under reduced pressure. Purification of the residue by column chromatography on silica gel (gradient heptane/EtOAc) afforded, after evaporation of the solvents, 59 mg (100% purity, 89% yield) of rac-5-(1-methylindol-3-yl)-3-[6-methyl-3-[3-(trifluoromethyl)phenoxy]pyridazin-4-yl]-5,6-dihydro-4H-1,2,4-oxadiazine as a pink solid.

Preparation of Example 5: Preparation of rac-5-[(4-bromo-2-chloro-phenyl)methyl]-3-[6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazin-4-yl]-5,6-dihydro-4H-1,2,4-oxadiazine (Compound 1.016) Step 1: Preparation of methyl 6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboximidate (Compound 25-02)

Under argon, sodium methanolate (32 mg, 0.59 mmol) was added at 0° C. to a solution of 6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carbonitrile (160 mg, 0.33 mmol) in MeOH (1.5 mL). The reaction mixture was stirred at 0° C. for 30 min. The crude solution contained 53% of methyl 6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboximidate and was used without further purification in the next step.

Step 2: Preparation of rac-5-[(4-bromo-2-chloro-phenyl)methyl]-3-[6-chloro-3-[3-(trifluoro-methyl)phenoxy]pyridazin-4-yl]-5,6-dihydro-4H-1,2,4-oxadiazine

To the previous solution was added O-[rac-2-amino-3-(4-bromo-2-chloro-phenyl)propyl]hydroxylamine (157 mg, 0.51 mmol) dissolved in MeOH/acetic acid (1 mL, 1:1). The reaction mixture was stirred at room temperature for 3 h then heated at 100° C. for 7 h. After cooling to room temperature, the mixture was poured into a saturated sodium bicarbonate solution and extracted with ethyl acetate (2×50 mL). The organic extracts were washed with brine, dried over sodium sulfate, filtered and concentrated under reduced pressure. Purification of the residue by preparative HPLC afforded, after evaporation of the solvents, 5 mg (93% purity, 2% yield) of rac-5-[(4-bromo-2-chloro-phenyl)methyl]-3-[6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazin-4-yl]-5,6-dihydro-4H-1,2,4-oxadiazine as an oil.

Preparation of Example 6: Preparation of rac-3-[6-chloro-3-(2-fluoro-3-methoxy-phenoxy)pyridazin-4-yl]-5-[(2,4-dimethylphenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazine (Compound 1.005) Step 1: Preparation of 3,6-dichloro-N-[rac-1-[(2,4-dimethylphenyl)methyl]-2-(1,3-dioxoisoindolin-2-yl)oxy-ethyl]pyridazine-4-carboxamide (Compound 6-01)

Under argon, to a solution of 3,6-dichloropyridazine-4-carboxylic acid (700 mg, 3.62 mmol) and HATU (1.52 g, 3.99 mmol) in DMF (25 mL) were successively added at 0° C., 2-[rac-2-amino-3-(2,4-dimethylphenyl)propoxy]isoindoline-1,3-dione; 2,2,2-trifluoroacetic acid (1.75 g, 4.0 mmol) and N,N-Diisopropylethylamine (1.89 mL, 10.88 mmol). After 15 min at 0° C., the reaction mixture was stirred for 18 h at room temperature. It was then diluted with water and extracted with ethyl acetate (2×200 mL). The organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure. Purification of the residue by column chromatography on silica gel (gradient heptane/EtOAc) afforded, after evaporation of the solvents, 1.15 g (87% purity, 55% yield) of 3,6-dichloro-N-[rac-1-[(2,4-dimethylphenyl)methyl]-2-(1,3-dioxoisoindolin-2-yl)oxy-ethyl]pyridazine-4-carboxamide as a white solid.

Step 2: Preparation of 3,6-dichloro-N-[rac-1-(aminooxymethyl)-2-(2,4-dimethylphenyl)ethyl]pyridazine-4-carboxamide (Compound 6-02)

Under argon, hydrazine monohydrate (0.42 mL, 6.91 mmol) was added to a solution of 3,6-dichloro-N-[rac-1-[(2,4-dimethylphenyl)methyl]-2-(1,3-dioxoisoindolin-2-yl)oxy-ethyl]pyridazine-4-carboxamide (1.15 g, 2.3 mmol) in DCM/MeOH (15 mL, 1:1). The reaction mixture was stirred for 3 h at room temperature and concentrated. It was then diluted with water and extracted with ethyl acetate (2×200 mL). The organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure. Evaporation of the solvents afforded 900 mg (74% purity, 78% yield) of 3,6-dichloro-N-[rac-1-(aminooxymethyl)-2-(2,4-dimethylphenyl)ethyl]pyridazine-4-carboxamide as a yellow solid.

Step 3: Preparation of rac-3-(3,6-dichloropyridazin-4-yl)-5-[(2,4-dimethylphenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazine (Compound 7-01)

Under argon, POCl₃ (0.56 mL, 6.0 mmol) was added at 80° C. to a solution of 3,6-dichloro-N-[rac-1-(aminooxymethyl)-2-(2,4-dimethylphenyl)ethyl]pyridazine-4-carboxamide (738 mg, 2.0 mmol) in AcCN (15 mL). The reaction mixture was stirred for 18 h at 80° C. After cooling to room temperature, the mixture was poured into a saturated sodium bicarbonate solution, then extracted with ethyl acetate (2×200 mL). The organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure. Purification of the residue by PREP-HPLC afforded, after evaporation of the solvents, 90 mg (92% purity, 17% yield) of rac-3-(3,6-dichloropyridazin-4-yl)-5-[(2,4-dimethylphenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazine as a yellow solid.

Step 4: Preparation of rac-3-[6-chloro-3-(2-fluoro-3-methoxy-phenoxy)pyridazin-4-yl]-5-[(2,4-dimethyl-phenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazine

To a solution of rac-3-(3,6-dichloropyridazin-4-yl)-5-[(2,4-dimethylphenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazine (60 mg, 0.17 mmol) in AcCN (1 mL) were added 2-fluoro-3-methoxy-phenol (27 mg, 0.19 mmol) and potassium carbonate (47 mg, 0.34 mmol). The reaction mixture was stirred at 50° C. for 5 h, then concentrated under reduced pressure. Purification of the residue by column chromatography on silica gel (gradient heptane/EtOAc) afforded, after evaporation of the solvents, 74 mg (97% purity, 90% yield) of rac-3-[6-chloro-3-(2-fluoro-3-methoxy-phenoxy)pyridazin-4-yl]-5-[(2,4-dimethylphenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazine as a yellow oil.

Preparation of Example 7: Preparation of 1-[5-[rac-5-[(2,4-dimethylphenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazin-3-yl]-6-[3-(trifluoromethyl)phenoxy]pyridazin-3-yl]ethanone (Compound 1.042) Step 1: Preparation of rac-5-[(2,4-dimethylphenyl)methyl]-3-[6-(1-ethoxyvinyl)-3-[3-(trifluoro-methyl)phenoxy]pyridazin-4-yl]-5,6-dihydro-4H-1,2,4-oxadiazine (Compound 1.009)

In a microwave vial, rac-3-[6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazin-4-yl]-5-[(2,4-dimethyl-phenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazine (500 mg, 1.05 mmol), tributyl(1-ethoxyvinyl)stannane (473 mg, 1.31 mmol) and bis(triphenylphosphine)palladium dichloride (73 mg, 0.103 mmol) were dissolved under argon in DMF (0.5 mL). The tube was sealed and the reaction mixture was heated in the microwave at 120° C. for 20 min. The reaction mixture was diluted with water and extracted with ethyl acetate (2×50 mL). The organic extracts were washed with water and brine, dried over magnesium sulfate, filtered and concentrated under reduced pressure. Purification of the residue by column chromatography on silica gel (gradient heptane/EtOAc) afforded, after evaporation of the solvents, 435 mg (100% purity, 80% yield) of rac-5-[(2,4-dimethylphenyl)methyl]-3-[6-(1-ethoxyvinyl)-3-[3-(trifluoromethyl)phenoxy]pyridazin-4-yl]-5,6-dihydro-4H-1,2,4-oxadiazine as an oil.

Step 2: Preparation of 1-[5-[rac-5-[(2,4-dimethylphenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazin-3-yl]-6-[3-(trifluoromethyl)phenoxy]pyridazin-3-yl]ethanone

To a solution of rac-5-[(2,4-dimethylphenyl)methyl]-3-[6-(1-ethoxyvinyl)-3-[3-(trifluoro-methyl)phenoxy]pyridazin-4-yl]-5,6-dihydro-4H-1,2,4-oxadiazine (100 mg, 0.19 mmol) in THF (1 mL) was added at room temperature a 2M aqueous HCl solution (0.15 mL, 0.30 mmol). The reaction was stirred for 30 min then diluted with water and extracted with ethyl acetate (2×50 mL). The organic extracts were washed with water and brine, dried over magnesium sulfate, filtered and concentrated under reduced pressure. Purification of the residue by column chromatography on silica gel (gradient heptane/EtOAc) afforded, after evaporation of the solvents, 35 mg (100% purity, 37% yield) of 1-[5-[rac-5-[(2,4-dimethylphenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazin-3-yl]-6-[3-(trifluoromethyl)phenoxy]pyridazin-3-yl]ethanone as a oil.

Preparation of Example 8: Preparation of 3-chloro-N-cyclopropyl-5-[rac-5-[(2,4-dimethylphenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazin-3-yl]-6-[3-(trifluoromethyl)phenoxy]pyridazin-4-amine (Compound 1.041) Step 1: Preparation of rac-3-[6-chloro-5-iodo-3-[3-(trifluoromethyl)phenoxy]pyridazin-4-yl]-5-[(2,4-dimethylphenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazine (Compound 1.065)

Under argon, a solution of TMPZnCl·LiCl (2.77 mmol, 5.1 mL, 17% in THF, CAS number 109-99-9) was added to rac-3-[6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazin-4-yl]-5-[(2,4-dimethylphenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazine (600 mg, 1.26 mmol) in THF (60 mL). After stirring 1 h at room temperature, NIS (566 mg, 2.52 mmol) was added portionwise. The reaction mixture was stirred 2 h at room temperature, then it was diluted with a saturated sodium thiosulfate solution and saturated sodium bicarbonate solution, and extracted with ethyl acetate (2×250 mL). The organic extracts were washed with brine, dried over magnesium sulfate, filtered and concentrated under reduced pressure. Purification of the residue by PREP-HPLC afforded, after evaporation of the solvents, 178 mg (70% purity, 16% yield) of rac-3-[6-chloro-5-iodo-3-[3-(trifluoromethyl)phenoxy]pyridazin-4-yl]-5-[(2,4-dimethylphenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazine as a yellow solid.

Step 2: Preparation of 3-chloro-N-cyclopropyl-5-[rac-5-[(2,4-dimethylphenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazin-3-yl]-6-[3-(trifluoromethyl)phenoxy]pyridazin-4-amine

Under argon, cyclopropylamine (6 mg, 0.10 mmol) and N,N-diisopropylethylamine (0.017 mL, 0.10 mmol) were added at room temperature to a solution of rac-3-[6-chloro-5-iodo-3-[3-(trifluoro-methyl)phenoxy]pyridazin-4-yl]-5-[(2,4-dimethylphenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazine (50 mg, 0.08 mmol) in AcCN (0.7 mL). The reaction mixture was stirred at 50° C. for 18 h, then it was diluted with water and extracted with ethyl acetate (2×50 mL). The organic extracts were washed with brine, dried over magnesium sulfate, filtered and concentrated under reduced pressure. Evaporation of the solvent afforded 42 mg (98% purity, 93% yield) of 3-chloro-N-cyclopropyl-5-[rac-5-[(2,4-dimethylphenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazin-3-yl]-6-[3-(trifluoromethyl)phenoxy]pyridazin-4-amine as an oil.

Preparation of Example 9: Preparation of 6-chloro-4-[rac-5-[(2,4-dichlorophenyl)methyl]-4,5-dihydro-1H-imidazol-2-yl]-3-[3-(trifluoromethyl)phenoxy]pyridazine (Compound 1.007)

A solution of POCl₃ (1.05 mL, 11.3 mmol) was added at room temperature to a mixture of 6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboxylic acid (400 mg, 1.25 mmol) and 3-(2,4-dichlorophenyl)propane-1,2-diamine (550 mg, 2.51 mmol) in 1,4-dioxane (10 mL). The reaction was heated to reflux and stirred for 36 h. After cooling, the reaction mixture was poured into a saturated sodium bicarbonate solution at 0° C., then extracted with ethyl acetate (2×100 mL). The organic extracts were washed with brine, dried over magnesium sulfate, filtered and concentrated under reduced pressure. Purification of the residue by PREP-HPLC afforded, after evaporation of the solvents, 90 mg (98% purity, 14% yield) of 6-chloro-4-[rac-5-[(2,4-dichlorophenyl)methyl]-4,5-dihydro-1H-imidazol-2-yl]-3-[3-(trifluoromethyl)phenoxy]pyridazine as a yellow oil.

Preparation of Example 10: preparation of (5S)-5-benzyl-3-[6-chloro-3-[3-(trifluoro-methyl)phenoxy]pyridazin-4-yl]-5,6-dihydro-4H-1,2,4-oxadiazine (compound I-070) Step 1: Preparation of 6-chloro-N-methoxy-N-methyl-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboxamide (Compound 1.03)

To a suspension of 6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboxylic acid (5.0 g, 16.7 mmol) in dichloromethane (75 mL) was added oxalyl chloride (3.19 g, 25.14 mmol) followed by two drops of DMF.

The reaction mixture was stirred at room temperature for 1 h. To the pre-formed acyl chloride was added N-methoxymethanamine; hydrochloride (2.12 g, 21.79 mmol) and triethylamine (8.17 mL, 58.68 mmol). The reaction mixture was stirred at room temperature for 2 h, then it was diluted with water and extracted with dichloromethane (2×200 mL). The organic extracts were washed with water and brine, dried over magnesium sulfate, filtered and concentrated under reduced pressure. The residue was diluted in dichloromethane and filtered over silica gel. Evaporation of the solvent afforded 3.38 g (95% purity, 56% yield) of 6-chloro-N-methoxy-N-methyl-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboxamide as a oil.

Step 2: Preparation of 6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carbaldehyde (Compound 16-01)

Under argon, a solution of DIBAL-H (0.88 mL, 0.88 mmol, 1M in hexan) was added at −50° C. to a solution of 6-chloro-N-methoxy-N-methyl-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboxamide (100 mg, 0.29 mmol) in THF (1.8 mL). After 4 h at −30° C., the reaction was stopped by addition of saturated ammonium chloride solution then the mixture was extracted with ethyl acetate (2×50 mL). The organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure. Purification of the residue by column chromatography on silica gel (gradient heptane/EtOAc) afforded, after evaporation of the solvents, 43.6 mg (90% purity, 47% yield) of 6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carbaldehyde as an oil.

Step 3: Preparation of 6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carbaldehyde oxime (Compound 17-01)

Under argon, hydroxylamine; hydrochloride (156 mg, 2.24 mmol) and potassium acetate (415 mg, 4.23 mmol) were added to 6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carbaldehyde (400 mg, 1.32 mmol) in EtOH (40 mL). The reaction mixture was stirred at reflux for 2 h, diluted in water and extracted with ethyl acetate (2×50 mL). The organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure. Evaporation of the solvents afforded 215 mg (90% purity, 47% yield) of 6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carbaldehyde oxime as a solid.

Step 4: preparation of (5S)-5-benzyl-3-[6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazin-4-yl]-5,6-dihydro-4H-1,2,4-oxadiazine

To a solution of 6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carbaldehyde oxime (10 mg, 0.031 mmol) in AcCN (0.2 mL) was added NCS (5.4 mg, 0.04 mmol) at room temperature. The reaction mixture was stirred for 1 h, then a solution of (2S)-1-bromo-3-phenyl-propan-2-amine; 2,2,2-trifluoroacetic acid (15.4 mg, 0.047 mmol) in AcCN/water (0.3 mL, 2:1) was added. The reaction was stirred at room temperature for 5 h then 1,2-bis(dimethylamino)ethane (18.3 mg, 0.16 mmol) was added to the reaction mixture. After 30 min, a solution of sodium carbonate (34 mg, 0.31 mmol, 1M in water) was added and the reaction was further stirred for 1 h at room temperature. The reaction mixture was diluted with water and dichloromethane and the aqueous phase was extracted with dichloromethane (2×50 mL). The organic layer was dried over sodium sulfate, filtered and concentrated under reduced pressure. Purification of the residue by preparative HPLC afforded, after evaporation of the solvents, 10.9 mg (85% purity, 65% yield) of (5S)-5-benzyl-3-[6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazin-4-yl]-5,6-dihydro-4H-1,2,4-oxadiazine as a yellow solid.

Preparation of Example 11: Preparation of rac-3-[6-chloro-5-(2-methoxyethoxy)-3-[3-(trifluoro-methyl)phenoxy]pyridazin-4-yl]-5-[(2,4-dimethylphenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazine (Compound 1.072)

Under argon, 2-methoxyethanol (0.15 mL, 0.30 mmol) and sodium hydride (11 mg, 0.27 mmol) were added at room temperature to a solution of rac-3-[6-chloro-5-iodo-3-[3-(trifluoromethyl)phenoxy]pyridazin-4-yl]-5-[(2,4-dimethylphenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazine (150 mg, 0.25 mmol) in AcCN (2 mL). The reaction mixture was stirred at room temperature for 1 h, then it was diluted with water and extracted with ethyl acetate (2×50 mL). The organic extracts were washed with brine, dried over magnesium sulfate, filtered and concentrated under reduced pressure. Purification of the residue by column chromatography on silica gel (gradient heptane/EtOAc) afforded, after evaporation of the solvents, 30 mg (90% purity, 19% yield) of rac-3-[6-chloro-5-(2-methoxyethoxy)-3-[3-(trifluoromethyl)phenoxy]pyridazin-4-yl]-5-[(2,4-dimethylphenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazine as a colorless oil.

Preparation of Example 12: Preparation of rac-3-[6-chloro-5-(4-pyridyl)-3-[3-(trifluoro-methyl)phenoxy]pyridazin-4-yl]-5-[(2,4-dimethylphenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazine (Compound 1.088)

Under argon, a solution of TMPZnCl·LiCl (0.22 mmol, 0.40 mL, 17% in THF, CAS number 109-99-9) was added to rac-3-[6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazin-4-yl]-5-[(2,4-dimethylphenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazine (50 mg, 0.10 mmol) in THF (3 mL), followed by addition of 4-bromopyridine (20 mg, 0.12 mmol), Pd(dba)₂ (18 mg, 0.031 mmol) and trifurylphosphine (15 m, 0.063 mmol). The reaction mixture was stirred 4 h at 60° C., then diluted with saturated ammonium chloride solution and saturated sodium bicarbonate solution, and extracted with ethyl acetate (2×100 mL). The organic extracts were washed with brine, dried over magnesium sulfate, filtered and concentrated under reduced pressure. Purification of the residue by PREP-HPLC afforded, after evaporation of the solvents, 32 mg (86% purity, 47% yield) of rac-3-[6-chloro-5-(4-pyridyl)-3-[3-(trifluoromethyl)phenoxy]pyridazin-4-yl]-5-[(2,4-dimethylphenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazine as an oil.

Preparation of Example 13: Preparation of rac-5-[(2,4-dimethylphenyl)methyl]-3-[6-(2-methoxyethylsulfanyl)-5-methyl-3-[3-(trifluoromethyl)phenoxy]pyridazin-4-yl]-5,6-dihydro-4H-1,2,4-oxadiazine (Compound 1.187)

Under argon, 2-methoxyethanethiol (20 mg, 0.22 mmol) and sodium hydride (8 mg, 0.22 mmol) were added at 0° C. to a solution of rac-3-[6-chloro-5-methyl-3-[3-(trifluoromethyl)phenoxy]pyridazin-4-yl]-5-[(2,4-dimethylphenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazine (100 mg, 0.20 mmol) in THF (2 mL). The reaction mixture was stirred at 0° C. for 2 h, then it was diluted with water and extracted with ethyl acetate (2×50 mL). The organic extracts were washed with brine, dried over magnesium sulfate, filtered and concentrated under reduced pressure. Purification of the residue by column chromatography on silica gel (gradient heptane/EtOAc) afforded, after evaporation of the solvents, 21 mg (96% purity, 18% yield) of rac-5-[(2,4-dimethylphenyl)methyl]-3-[6-(2-methoxyethylsulfanyl)-5-methyl-3-[3-(trifluoromethyl)phenoxy]pyridazin-4-yl]-5,6-dihydro-4H-1,2,4-oxadiazine as a colorless oil.

Preparation of Example 14: Preparation of rac-2-[6-chloro-3-(3-cyclopropylphenoxy)pyridazin-4-yl]-6-[(2,4-dimethylphenyl)methyl]-5,6-dihydro-1H-pyrimidin-4-one (Compound 1.078) Step 1: preparation of methyl 6-chloro-3-(3-cyclopropylphenoxy)pyridazine-4-carboximidate (compound 25-01)

Under argon, sodium methanolate (43 mg, 0.81 mmol) was added at 0° C. to a solution of 6-chloro-3-(3-cyclopropylphenoxy)pyridazine-4-carbonitrile (200 mg, 0.74 mmol) in MeOH (2 mL). The reaction mixture was stirred at 0° C. for 30 min. The crude solution contained 48% of methyl 6-chloro-3-(3-cyclopropylphenoxy)pyridazine-4-carboximidate and was used without further purification in the next step.

Step 2: Preparation of rac-2-[6-chloro-3-(3-cyclopropylphenoxy)pyridazin-4-yl]-6-[(2,4-dimethyl-phenyl)methyl]-5,6-dihydro-1H-pyrimidin-4-one

To the previous solution was added rac-3-amino-4-(2,4-dimethylphenyl)butanamide (93 mg, 0.45 mmol) dissolved in MeOH (0.5 mL) and acetic acid (17 μL). The reaction mixture was stirred at room temperature for 15 min then heated at 60° C. for 18 h. After cooling to room temperature, the mixture was poured into a saturated sodium bicarbonate solution and extracted with ethyl acetate (2×50 mL). The organic extracts were washed with brine, dried over sodium sulfate, filtered and concentrated under reduced pressure. Purification of the residue by preparative HPLC afforded, after evaporation of the solvents, 40.7 mg (100% purity, 29% yield) of rac-2-[6-chloro-3-(3-cyclopropylphenoxy)pyridazin-4-yl]-6-[(2,4-dimethylphenyl)methyl]-5,6-dihydro-1H-pyrimidin-4-one as an oil.

Preparation of Example 15: Preparation of rac-5-[(2,4-dimethylphenoxy)methyl]-3-[6-methyl-3-[3-(trifluoromethyl)phenoxy]pyridazin-4-yl]-5,6-dihydro-4H-1,2,4-oxadiazine (Compound 1.144) Step 1: preparation of tert-butyl rac-4-[(2,4-dimethylphenoxy)methyl]-2,2-dimethyl-oxazolidine-3-carboxylate

Under argon, diisopropyl azodicarboxylate (1.92 g, 9.51 mmol) was added to a solution of tert-butyl rac-4-(hydroxymethyl)-2,2-dimethyl-oxazolidine-3-carboxylate (2.0 g, 8.64 mmol), 2,4-dimethylphenol (1.16 g, 9.51 mmol) and triphenylphosphine (2.49 g, 9.51 mmol) in 2-methyltetrahydrofuran (30 mL). The reaction mixture was heated at 80° C. for 3 h, cooled to room temperature and extracted with ethyl acetate (2×200 mL). The organic layer was washed with 1M aqueous NaOH solution and brine, dried over magnesium sulfate, filtered and concentrated under reduced pressure. Purification of the residue by column chromatography on silica gel (gradient heptane/EtOAc) afforded, after evaporation of the solvents, 1.82 g (95% purity, 59% yield) of tert-butyl rac-4-[(2,4-dimethylphenoxy)methyl]-2,2-dimethyl-oxazolidine-3-carboxylate as a colorless oil.

Step 2: Preparation of rac-2-amino-3-(2,4-dimethylphenoxy)propan-1-ol

A solution of tert-butyl rac-4-[(2,4-dimethylphenoxy)methyl]-2,2-dimethyl-oxazolidine-3-carboxylate (1.8 g, 5.37 mmol) was dissolved in MeOH (25 mL) and aqueous 1M HCl solution (15 mL). The reaction mixture was stirred at 50° C. for 2 h. After cooling to room temperature, the solvents were evaporated and the residue was poured into a saturated sodium bicarbonate solution and extracted with ethyl acetate (2×200 mL). The organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure. Evaporation of the solvents afforded 833 mg (87% purity, 69% yield) of rac-2-amino-3-(2,4-dimethylphenoxy)propan-1-ol as a yellow oil.

Step 3: preparation of tert-butyl N-[rac-1-[(2,4-dimethylphenoxy)methyl]-2-hydroxy-ethyl]carbamate

Di-tert-butyl dicarbonate (1.02 mL, 4.46 mmol) and N,N-Diisopropylethylamine (1.55 mL, 8.93 mmol) were successively added to a solution of rac-2-amino-3-(2,4-dimethylphenoxy)propan-1-ol (830 mg, 4.25 mmol) in 2-methyltetrahydrofuran (5.5 mL). The reaction mixture was stirred at room temperature for 1 h30, then it was diluted with brine and extracted with ethyl acetate (2×200 mL). The organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure. Purification of the residue by column chromatography on silica gel (gradient heptane/EtOAc) afforded, after evaporation of the solvents, 909 mg (97% purity, 70% yield) of tert-butyl N-[rac-1-[(2,4-dimethylphenoxy)methyl]-2-hydroxy-ethyl]carbamate as a colorless oil.

Step 4: Preparation of tert-butyl N-[rac-1-[(2,4-dimethylphenoxy)methyl]-2-(1,3-dioxoisoindolin-2-yl)oxy-ethyl]carbamate (Compound 2-13)

Under argon, diisopropyl azodicarboxylate (684 mg, 3.38 mmol) was added to a solution of tert-butyl N-[rac-1-[(2,4-dimethylphenoxy)methyl]-2-hydroxy-ethyl]carbamate (909 mg, 3.0 mmol), N-hydroxyphthalimide (552.2 mg, 3.38 mmol) and triphenylphosphine (888 mg, 3.38 mmol) in 2-methyltetrahydrofuran (10 mL). The reaction mixture was stirred at room temperature for 2 h, then extracted with ethylacetate (2×200 mL). The organic layer was washed with 1M aqueous NaOH solution and brine, dried over magnesium sulfate, filtered and concentrated under reduced pressure. Purification of the residue by column chromatography on silica gel (gradient heptane/EtOAc) afforded, after evaporation of the solvents, 1.16 g (92% purity, 79% yield) of tert-butyl N-[rac-1-[(2,4-dimethylphenoxy)methyl]-2-(1,3-dioxoisoindolin-2-yl)oxy-ethyl]carbamate as a colorless oil.

Step 5: Preparation of 2-[rac-2-amino-3-(2,4-dimethylphenoxy)propoxy]isoindoline-1,3-dione 2,2,2-trifluoroacetate (Compound 2-12)

To a solution of tert-butyl N-[rac-1-[(2,4-dimethylphenoxy)methyl]-2-(1,3-dioxoisoindolin-2-yl)oxy-ethyl]carbamate (1.16 g, 2.63 mmol) in 1,2-dichloroethane (15 mL) was added trifluoroacetic acid (1.014 mL, 13.17 mmol). The reaction mixture was stirred at room temperature for 4 h. Evaporation of the solvents afforded 1.4 g (79% purity, 93% yield) of 2-[rac-2-amino-3-(2,4-dimethylphenoxy)propoxy]isoindoline-1,3-dione; 2,2,2-trifluoroacetic acid as a yellow oil.

Step 6: Preparation of 6-methyl-N-[rac-1-[(2,4-dimethylphenoxy)methyl]-2-(1,3-dioxoisoindolin-2-yl)oxy-ethyl]-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboxamide (Compound 3-33)

Under argon, to a solution of 6-methyl-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboxylic acid (405 mg, 1.36 mmol) and HATU (542 mg, 1.42 mmol) in DMF (10 mL) were successively added 2-[rac-2-amino-3-(2,4-dimethylphenoxy)propoxy]isoindoline-1,3-dione; 2,2,2-trifluoroacetic acid (647 mg, 1.42 mmol) and N,N-Diisopropylethylamine (0.71 mL, 4.07 mmol). The reaction mixture was stirred for 1 h at room temperature. It was then diluted with water and extracted with ethyl acetate (2×200 mL). The organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure. Purification of the residue by column chromatography on silica gel (gradient heptane/EtOAc) afforded, after evaporation of the solvents, 550 mg (93% purity, 60% yield) of 6-methyl-N-[rac-1-[(2,4-dimethylphenoxy)methyl]-2-(1,3-dioxoisoindolin-2-yl)oxy-ethyl]-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboxamide as a colorless oil.

Step 7: Preparation of 6-methyl-N-[rac-1-(aminooxymethyl)-2-(2,4-dimethylphenoxy)ethyl]-3-[3-(trifluoro-methyl)phenoxy]pyridazine-4-carboxamide (Compound 4-33)

Under argon, hydrazine monohydrate (0.16 mL, 2.66 mmol) was added to a solution of 6-methyl-N-[rac-1-[(2,4-dimethylphenoxy)methyl]-2-(1,3-dioxoisoindolin-2-yl)oxy-ethyl]-3-[3-(trifluoro-methyl)phenoxy]pyridazine-4-carboxamide (550 mg, 0.89 mmol) in DCM/MeOH (16 mL, 1:1). The reaction mixture was stirred for 2 h at room temperature then concentrated. The residue was diluted with water and extracted with dichloromethane (2×200 mL). The organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure. Evaporation of the solvents afforded 490 mg (75% purity, 84% yield) of 6-methyl-N-[rac-1-(aminooxymethyl)-2-(2,4-dimethylphenoxy)ethyl]-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboxamide as a white oil.

Step 8: Preparation of rac-5-[(2,4-dimethylphenoxy)methyl]-3-[6-methyl-3-[3-(trifluoro-methyl)phenoxy]pyridazin-4-yl]-5,6-dihydro-4H-1,2,4-oxadiazine

Under argon, POCl₃ (0.22 mL, 2.39 mmol) was added at 80° C. to a solution of 6-methyl-N-[rac-1-(aminooxymethyl)-2-(2,4-dimethylphenoxy)ethyl]-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboxamide (490 mg, 0.80 mmol) in AcCN (10 mL). The reaction mixture was stirred for 4 h at 80° C. After cooling to room temperature, the mixture was poured into a saturated sodium bicarbonate solution, then extracted with ethyl acetate (2×200 mL). The organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure. Purification of the residue by column chromatography on silica gel (gradient heptane/EtOAc) afforded, after evaporation of the solvents, 89 mg (95% purity, 22% yield) of rac-5-[(2,4-dimethylphenoxy)methyl]-3-[6-methyl-3-[3-(trifluoromethyl)phenoxy]pyridazin-4-yl]-5,6-dihydro-4H-1,2,4-oxadiazine as a brown oil.

Preparation of Example 16: Preparation of rac-5-(1-methylindol-5-yl)-3-[6-methyl-3-[3-(trifluoro-methyl)phenoxy]pyridazin-4-yl]-4,5,6,7-tetrahydro-1,2,4-oxadiazepine (Compound 1.062) Step 1: preparation of N′-allyloxy-6-methyl-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboxamidine

In analogy to step 1 of example 4.

Step 2: Preparation of 6-methyl-N′-[3-(1-methylindol-5-yl)allyloxy]-3-[3-(trifluoro-methyl)phenoxy]pyridazine-4-carboxamidine (Compound 30-01)

Under argon, a mixture of N′-allyloxy-6-methyl-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboxamidine (500 mg, 1.42 mmol), 5-bromo-1-methyl-indole (596 mg, 2.83 mmol), triethylamine (0.40 mL, 2.84 mmol), palladium(II) acetate (32 mg, 0.14 mmol) and tri-2tolylphosphine (86 mg, 0.28 mmol) in AcCN (5 mL) was stirred at reflux for 18 h. After cooling to room temperature, the reaction mixture was diluted with a saturated ammonium chloride solution and extracted with ethyl acetate (3×30 mL). Purification of the residue by column chromatography on silica gel (gradient heptane/EtOAc) afforded, after evaporation of the solvents, 203 mg (93% purity, 27% yield) of 6-methyl-N′-[3-(1-methylindol-5-yl)allyloxy]-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboxamidine as an oil.

Step 3: Preparation of rac-5-(1-methylindol-5-yl)-3-[6-methyl-3-[3-(trifluoromethyl)phenoxy]pyridazin-4-yl]-4,5,6,7-tetrahydro-1,2,4-oxadiazepine

A solution of iodine (13.2 mg, 0.052 mmol) and phenylsilane (11.2 mg, 0.104 mmol) in dichloromethane (5 mL) was stirred at room temperature for 30 min, then 6-methyl-N′-[3-(1-methylindol-5-yl)allyloxy]-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboxamidine (25.0 mg, 0.052 mmol) was added. The reaction mixture was stirred for 1 h, then diluted with a saturated sodium thiosulfate solution and extracted with ethyl acetate (2×50 mL). The organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure. Purification of the residue by PREP-HPLC afforded, after evaporation of the solvents, 8 mg (88% purity, 28% yield) of rac-5-(1-methylindol-5-yl)-3-[6-methyl-3-[3-(trifluoromethyl)phenoxy]pyridazin-4-yl]-4,5,6,7-tetrahydro-1,2,4-oxadiazepine as an oil.

Preparation of Example 17: Preparation of rac-3-[6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazin-4-yl]-5-[(2,4-dimethylphenyl)methyl]-1,4,5,6-tetrahydro-1,2,4-triazine (Compound I.173) Step 1: Preparation of 6-chloro-N-[1-(chloromethyl)-2-(2,4-dimethylphenyl)ethyl]-3-[3-(trifluoro-methyl)phenoxy]pyridazine-4-carboxamide

See step 1 of example 2.

Step 2: Preparation of rac-3-[6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazin-4-yl]-5-[(2,4-dimethyl-phenyl)methyl]-1,4,5,6-tetrahydro-1,2,4-triazine

To a solution of 6-chloro-N-[1-(chloromethyl)-2-(2,4-dimethylphenyl)ethyl]-3-[3-(trifluoro-methyl)phenoxy]pyridazine-4-carboxamide (339 mg, 0.68 mmol) in toluene (6 mL) was added phosphorous pentachloride (425 mg, 2.04 mmol). The reaction mixture was stirred at 75° C. for 1 h30, then concentrated under reduced pressure. The residue was dissolved in AcCN (4 mL) and a solution of hydrazine hydrate (170.27 mg, 3.40 mmol) was added at room temperature to the reaction mixture. After stirring at room temperature for 1 h the reaction mixture was diluted with water and extracted with ethyl acetate (2×100 mL). The organic extracts were washed with water and brine, dried over sodium sulfate, filtered and concentrated under reduced pressure. Purification of the residue by column chromatography on silica gel (gradient heptane/EtOAc) afforded, after evaporation of the solvents, 197 mg (100% purity, 60% yield) of rac-3-[6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazin-4-yl]-5-[(2,4-dimethylphenyl)methyl]-1,4,5,6-tetrahydro-1,2,4-triazine.

Preparation of Example 18: Preparation of 6-chloro-4-[rac-6-[(2,4-dimethylphenyl)methyl]-1,4,5,6-tetrahydropyrimidin-2-yl]-3-[3-(trifluoromethyl)phenoxy]pyridazine (Compound 1.117) Step 1: preparation of tert-butyl N-[rac-1-[(2,4-dimethylphenyl)methyl]-3-hydroxy-propyl]carbamate

Di-tert-butyl dicarbonate (2.13 g, 9.79 mmol) and triethylamine (2.73 mL, 19.6 mmol) were successively added at 0° C. to a suspension of rac-3-amino-4-(2,4-dimethylphenyl)butan-1-ol hydrochloride (1.5 g, 6.52 mmol) in tetrahydrofuran (10 mL). The reaction mixture was stirred at room temperature for 18 h, then concentrated under reduced pressure. Purification of the residue by column chromatography on silica gel (gradient heptane/EtOAc) afforded, after evaporation of the solvents, 1.8 g (97% purity, 91% yield) of tert-butyl N-[rac-1-[(2,4-dimethylphenyl)methyl]-3-hydroxy-propyl]carbamate as a white solid.

Step 2: preparation of tert-butyl N-[rac-1-[(2,4-dimethylphenyl)methyl]-3-(1,3-dioxoisoindolin-2-yl)propyl]carbamate

Under argon, diethyl azodicarboxylate (6.87 g, 15.3 mmol) was added at 0° C. to a solution of tert-butyl N-[rac-1-[(2,4-dimethylphenyl)methyl]-3-hydroxy-propyl]carbamate (1.8 g, 6.13 mmol), phthalimide (5.41 g, 36.8 mmol) and triphenylphosphine (9.65 g, 36.8 mmol) in tetrahydrofuran (200 mL). The reaction mixture was stirred at room temperature for 24 h, diluted with water and extracted with ethylacetate (3×200 mL). The organic layer was washed with brine, dried over magnesium sulfate, filtered and concentrated under reduced pressure. Purification of the residue by column chromatography on silica gel (gradient heptane/EtOAc) afforded, after evaporation of the solvents, 2.0 g (84% purity, 60% yield) of tert-butyl N-[rac-1-[(2,4-dimethylphenyl)methyl]-3-(1,3-dioxoisoindolin-2-yl)propyl]carbamate as a colorless oil.

Step 3: Preparation of 2-[rac-3-amino-4-(2,4-dimethylphenyl)butyl]isoindoline-1,3-dione; 2,2,2-trifluoroacetate

To a solution of tert-butyl N-[rac-1-[(2,4-dimethylphenyl)methyl]-3-(1,3-dioxoisoindolin-2-yl)propyl]carbamate (1.2 g, 2.84 mmol) in dichloromethane (20 mL) was added trifluoroacetic acid (0.65 mL, 8.52 mmol). The reaction mixture was stirred at room temperature for 3 days. Evaporation of the solvents afforded 1.2 g (54% purity, 52% yield) of 2-[rac-3-amino-4-(2,4-dimethylphenyl)butyl]isoindoline-1,3-dione; 2,2,2-trifluoroacetic acid as a solid.

Step 4: Preparation of rac-4-(2,4-dimethylphenyl)butane-1,3-diamine

Under argon, hydrazine monohydrate (3.73 mL, 41.24 mmol) was added to a solution of 2-[rac-3-amino-4-(2,4-dimethylphenyl)butyl]isoindoline-1,3-dione; 2,2,2-trifluoroacetic acid (1.2 g, 2.75 mmol) in EtOH (5 mL). The reaction mixture was stirred for 3 days at room temperature then concentrated. It was then diluted with water and extracted with dichloromethane (2×200 mL). The organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure. The residue was stirred in MTBE and the white solid that formed was filtered off. Concentration of the filtrate afforded 520 mg (95% purity, 93% yield) of rac-4-(2,4-dimethylphenyl)butane-1,3-diamine as a white solid.

Step 5: Preparation of methyl 6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboximidate

See step 1 of example 5 starting from 6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carbonitrile (100 mg, 0.33 mmol)

Step 6: Preparation of 6-chloro-4-[rac-6-[(2,4-dimethylphenyl)methyl]-1,4,5,6-tetrahydropyrimidin-2-yl]-3-[3-(trifluoromethyl)phenoxy]pyridazine

To the previous solution of methyl 6-chloro-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboximidate was added at 0° C. rac-4-(2,4-dimethylphenyl)butane-1,3-diamine (124 mg, 0.45 mmol) dissolved in MeOH (0.5 mL) and acetic acid (9 μL). The reaction mixture was stirred at room temperature for 5 h, then the mixture was poured into a saturated sodium bicarbonate solution and extracted with ethyl acetate (2×50 mL). The organic extracts were washed with brine, dried over sodium sulfate, filtered and concentrated under reduced pressure. Purification of the residue by column chromatography on silica gel (gradient heptane/EtOAc) afforded, after evaporation of the solvents, 26 mg (90% purity, 16% yield) of 6-chloro-4-[rac-6-[(2,4-dimethylphenyl)methyl]-1,4,5,6-tetrahydropyrimidin-2-yl]-3-[3-(trifluoromethyl)phenoxy]pyridazine as a yellow oil.

Preparation of Example 19: Preparation of rac-6,6-difluoro-5-(4-methoxyphenyl)-3-[6-methyl-3-[3-(trifluoromethyl)phenoxy]pyridazin-4-yl]-4,5-dihydro-1,2,4-oxadiazine (Compound I.154) Step 1: preparation of N′-hydroxy-6-methyl-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboxamidine (Compound 10-02)

See step 3 of example 3

Step 2: Preparation of N′-[1,1-difluoro-2-(4-methoxyphenyl)-2-oxo-ethoxy]-6-methyl-3-[3-(trifluoro-methyl)phenoxy]pyridazine-4-carboxamidine (Compound 12-14)

Under argon, 2-tert-butylimino-N,N-diethyl-1,3-dimethyl-1,3,2lambda5-diazaphosphinan-2-amine (BEMP) (105 mg, 0.38 mmol) was added at room temperature to a solution of N′-hydroxy-6-methyl-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboxamidine (100 mg, 0.32 mmol) in AcCN (1.5 mL). After 15 min, 2-bromo-2,2-difluoro-1-(4-methoxyphenyl)ethanone (127 mg, 0.48 mmol) was added and the reaction was stirred further for 15 min. The reaction mixture was diluted with a saturated ammonium chloride solution and extracted with ethyl acetate (2×50 mL). The organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure. Evaporation of the solvents afforded 222 mg (27% purity, 80% yield) of N′-[1,1-difluoro-2-(4-methoxyphenyl)-2-oxo-ethoxy]-6-methyl-3-[3-(trifluoromethyl)phenoxy]pyridazine-4-carboxamidine as an oil.

Step 3: Preparation of rac-6,6-difluoro-5-(4-methoxyphenyl)-3-[6-methyl-3-[3-(trifluoro-methyl)phenoxy]pyridazine-4-yl]-4,5-dihydro-1,2,4-oxadiazine

Under argon, N′-[1,1-difluoro-2-(4-methoxyphenyl)-2-oxo-ethoxy]-6-methyl-3-[3-(trifluoro-methyl)phenoxy]pyridazine-4-carboxamidine (222 mg, 0.25 mmol) was dissolved in tert-butanol (6.4 mL) and acetic acid (1.6 mL) and heated to 80° C. After 30 min, sodium cyanoborohydride (21 mg, 0.34 mmol) was added and the reaction was stirred further for 2 h. After cooling to room temperature, the mixture was poured into a 1M aqueous NaOH solution and extracted with ethyl acetate (2×20 mL). The organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure. Purification of the residue by PREP-HPLC afforded, after evaporation of the solvents, 4 mg (96% purity, 3% yield) of rac-6,6-difluoro-5-(4-methoxyphenyl)-3-[6-methyl-3-[3-(trifluoromethyl)phenoxy]pyridazin-4-yl]-4,5-dihydro-1,2,4-oxadiazine as a yellow solid.

Preparation of Example 20: Preparation of rac-3-[6-chloro-3-(3-cyclopropyl-2-fluoro-phenoxy)-5-methyl-pyridazin-4-yl]-5-[(2,4-dimethylphenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazine (Compound 1.058) Step 1: preparation of isopropyl 6-chloro-3-(3-cyclopropyl-2-fluoro-phenoxy)-5-methyl-pyridazine-4-carboxylate (Compound 1-24)

To a solution of isopropyl 6-chloro-3-(3-cyclopropyl-2-fluoro-phenoxy)pyridazine-4-carboxylate (800 mg, 2.28 mmol) in dimethyl sulfoxide (2.5 mL) was added nitromethane (0.62 mL, 11.40 mmol). The reaction was stirred at room temperature for 30 min, then triethylamine (0.48 mL, 3.42 mmol) was added. The reaction was stirred at room temperature for 24 h, then it was diluted with water and extracted with ethyl acetate (2×100 mL). The organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure. Evaporation of the solvents afforded 917 mg (76% purity, 84% yield) of isopropyl 6-chloro-3-(3-cyclopropyl-2-fluoro-phenoxy)-5-methyl-pyridazine-4-carboxylate as an orange oil.

Step 2: Preparation of 6-chloro-3-(3-cyclopropyl-2-fluoro-phenoxy)-5-methyl-pyridazine-4-carboxylic acid (Compound 1-02)

To a solution of isopropyl 6-chloro-3-(3-cyclopropyl-2-fluoro-phenoxy)-5-methyl-pyridazine-4-carboxylate (927 mg, 2.5 mmol) in tetrahydrofuran (4 mL) was added a 2M aqueous solution of lithium hydroxide (182 mg, 7.62 mmol). The reaction was stirred for 4 days at room temperature then it was diluted with water. The aqueous phase was acidified with 1M aqueous HCl solution and extracted with ethyl acetate (3×200 mL). The organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure. Evaporation of the solvents afforded 617 mg (81% purity, 60% yield) of 6-chloro-3-(3-cyclopropyl-2-fluoro-phenoxy)-5-methyl-pyridazine-4-carboxylic acid as a solid.

Step 3: Preparation of 6-chloro-3-(3-cyclopropyl-2-fluoro-phenoxy)-5-methyl-N-[rac-1-[(2,4-dimethyl-phenyl)methyl]-2-(1,3-dioxoisoindolin-2-yl)oxy-ethyl]pyridazine-4-carboxamide

Under argon, to a solution of 6-chloro-3-(3-cyclopropyl-2-fluoro-phenoxy)-5-methyl-pyridazine-4-carboxylic acid (500 mg, 1.55 mmol) and HATU (648 mg, 1.70 mmol) in DMF (10 mL) were successively added at 0° C., 2-[rac-2-amino-3-(2,4-dimethylphenyl)propoxy]isoindoline-1,3-dione 2,2,2-trifluoroacetate (747 mg, 1.70 mmol) and N,N-Diisopropylethylamine (0.80 mL, 4.64 mmol). After 15 min at 0° C., the reaction mixture was stirred for 18 h at room temperature. It was then diluted with water and extracted with ethyl acetate (2×200 mL). The organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure. Purification of the residue by column chromatography on silica gel (gradient heptane/EtOAc) afforded, after evaporation of the solvents, 639.5 g (100% purity, 65% yield) of 6-chloro-3-(3-cyclopropyl-2-fluoro-phenoxy)-5-methyl-N-[rac-1-[(2,4-dimethylphenyl)methyl]-2-(1,3-dioxoisoindolin-2-yl)oxy-ethyl]pyridazine-4-carboxamide as a solid.

Step 4: Preparation of 6-chloro-3-(3-cyclopropyl-2-fluoro-phenoxy)-5-methyl-N-[rac-1-(aminooxymethyl)-2-(2,4-dimethylphenyl)ethyl]pyridazine-4-carboxamide

Under argon, hydrazine monohydrate (0.18 mL, 3.0 mmol) was added to a solution of 6-chloro-3-(3-cyclopropyl-2-fluoro-phenoxy)-5-methyl-N-[rac-1-[(2,4-dimethylphenyl)methyl]-2-(1,3-dioxoisoindolin-2-yl)oxy-ethyl]pyridazine-4-carboxamide (639 mg, 1.0 mmol) in DCM/MeOH (12 mL, 1:1). The reaction mixture was stirred for 18 h at room temperature and concentrated. It was then diluted with water and extracted with dichloromethane (2×200 mL). The organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure. Evaporation of the solvents afforded 453 mg (100% purity, 89% yield) of 6-chloro-3-(3-cyclopropyl-2-fluoro-phenoxy)-5-methyl-N-[rac-1-(aminooxymethyl)-2-(2,4-dimethylphenyl)ethyl]pyridazine-4-carboxamide as a white oil.

Step 5: Preparation of rac-3-[6-chloro-3-(3-cyclopropyl-2-fluoro-phenoxy)-5-methyl-pyridazin-4-yl]-5-[(2,4-dimethylphenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazine

Under argon, POCl₃ (0.25 mL, 2.72 mmol) was added at 80° C. to a solution 6-chloro-3-(3-cyclopropyl-2-fluoro-phenoxy)-5-methyl-N-[rac-1-(aminooxymethyl)-2-(2,4-dimethylphenyl)ethyl]pyridazine-4-carboxamide (453 mg, 0.90 mmol) in AcCN (5 mL). The reaction mixture was stirred for 18 h at 80° C. After cooling to room temperature, the mixture was poured into a saturated sodium bicarbonate solution, then extracted with ethyl acetate (2×200 mL). The organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure. Purification of the residue by column chromatography on silica gel (gradient heptane/EtOAc) afforded, after evaporation of the solvents, 196 mg (100% purity, 44% yield) of rac-3-[6-chloro-3-(3-cyclopropyl-2-fluoro-phenoxy)-5-methyl-pyridazin-4-yl]-5-[(2,4-dimethylphenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazine as a yellow solid.

The compounds as shown in table 1 below were prepared in analogy with the examples provided above or following methods described herein. ¹H-NMR data of these compounds is shown in table 2.

TABLE 1 Compounds according to formula (I)

wherein

in table 1 has the following meanings:

In table 1, “#” denotes the point of attachment to the L—R⁶ group and “*” denotes the point of attachment to the pyridazin-4-yl group. Ex N^(o) R⁷ R⁸ Q

L—R⁶ LogP I-001 chloro H 3-cyclopropyl-2-fluorophenyl Ring 1 (2,4-dimethylphenyl)methyl 4.61^([a]) I-002 methylamino H 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 2.84^([a]) I-003 chloro H 3-(trifluoromethyl)phenyl Ring 1 (4-chlorophenyl)methyl 3.99^([a]); 3.96^([b]) I-004 methyl H 2-fluoro-3-(trifluoromethyl) Ring 1 (2,4-dimethylphenyl)methyl 3.99^([a]) phenyl I-005 chloro H 2-fluoro-3-methoxyphenyl Ring 1 (2,4-dimethylphenyl)methyl 3.91^([a]) I-006 methyl methoxy 3-chlorophenyl Ring 1 (2,4-dimethylphenyl)methyl 3.50^([a]) I-007 chloro H 3-(trifluoromethyl)phenyl Ring 2 (2,4-dichlorophenyl)methyl 2.39^([a]) I-008 cyclopropyl- H 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 3.17^([a]) amino I-009 1-ethoxyethen- H 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.98^([a]) 1-yl I-010 methyl H 3-(trifluoromethyl)phenyl Ring 1 2,4-dichlorophenyl 3.85^([a]); 3.80^([b]) I-011(*) methyl H 3-(trifluoromethyl)phenyl Ring 1 1-methyl-1H-indol-3-yl 3.23^([a]) I-012 ethyl H 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.20^([a]) I-013(*) methyl H 3-(difluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 3.29^([a]) I-014 vinyl H 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.25^([a]) I-015 methyl H 3-(trifluoromethyl)phenyl Ring 1 naphthalen-2-yl 3.48^([a]) I-016(*) chloro H 3-(trifluoromethyl)phenyl Ring 1 (4-bromo-2-chlorophenyl)methyl 4.61^([a]) I-017(*) chloro H 3-(trifluoromethyl)phenyl Ring 1 (4-bromo-2-methylphenyl)methyl 4.49^([a]) I-018 methyl H 3-(trifluoromethyl)phenyl Ring 1 3,4-dimethylphenyl 3.58^([a]) I-019 chloro H 3-(trifluoromethyl)phenyl Ring 1 (4-cyclopropyl-2-methylphenyl)methyl 4.67^([a]) I-020 chloro H 3-(trifluoromethyl)phenyl Ring 1 (2-chloro-4-cyclopropylphenyl)methyl 4.74^([a]) I-021 chloro H 3-(trifluoromethyl)phenyl Ring 1 (2-chloro-4-isopropylphenyl)methyl 5.11^([a]) I-022 chloro H 3-(trifluoromethyl)phenyl Ring 1 (3,4-dimethylphenyl)methyl 4.41^([a]) I-023 chloro H 3-(trifluoromethyl)phenyl Ring 1 (4-isopropyl-2-methylphenyl)methyl 5.03^([a]) I-024 chloro H 3-(difluoromethyl)-2- Ring 1 (2,4-dimethylphenyl)methyl 4.08^([a]) fluorophenyl I-025(*) chloro H 3-(trifluoromethyl)phenyl Ring 1 (2,4-dichlorophenyl)methyl 4.51^([a]) I-026 methyl H 3-(trifluoromethyl)phenyl Ring 3 3-methylphenyl 3.30^([a]) I-027(*) methyl H 3-cyclopropyl-2-fluorophenyl Ring 1 (4-bromo-2-chlorophenyl)methyl 4.28^([a]) I-028 methyl H 3-(difluoromethyl)phenyl Ring 1 (2,4-dichlorophenyl)methyl 3.50^([a]) I-029 methyl H 3-(trifluoromethyl)phenyl Ring 1 furan-2-yl 2.62^([a]) I-030(*) methyl H 3-cyclopropyl-2-fluorophenyl Ring 1 (2,4-dichlorophenyl)methyl 4.23^([a]) I-031 methyl H 3-(trifluoromethyl)phenyl Ring 1 phenyl 2.94^([a]) I-032 methyl H 3-(trifluoromethyl)phenyl Ring 1 (2-chloro-4-isopropylphenyl)methyl 4.56^([a]) I-033 chloro H 3-(2,2-difluorocyclopropyl) Ring 1 (4-bromo-2-chlorophenyl)methyl 4.42^([a]) phenyl I-034 chloro methyl 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.12^([a]) I-035 methyl H 3-(trifluoromethyl)phenyl Ring 1 (4-isopropyl-2-methylphenyl)methyl 4.49^([a]) I-036 methyl H 2-fluoro-3-(trifluoromethyl) Ring 1 (2,4-dichlorophenyl)methyl 4.03^([a]) phenyl I-037 chloro methylamino 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 3.69^([a]) I-038 methyl H 3-(trifluoromethyl)phenyl Ring 1 (2-chloro-4-cyclopropylphenyl)methyl 4.18^([a]) I-039 chloro H 3-(1-fluorocyclopropyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.34^([a]) I-040 methyl H 3-(trifluoromethyl)phenyl Ring 1 4-chlorophenyl 3.29^([a]) I-041 chloro cyclopropylamino 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.03^([a]) I-042 acetyl H 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.27^([a]) I-043 methyl chloro 3-chlorophenyl Ring 1 (2,4-dimethylphenyl)methyl 3.83^([a]) I-044 chloro H 3-(2,2-difluorocyclopropyl) Ring 1 (2,4-dimethylphenyl)methyl 4.24^([a]) phenyl I-045 methyl H 3-cyclopropyl-2-fluorophenyl Ring 1 (3,4-dimethylphenyl)methyl 4.01^([a]) I-046 pyridin-4-yl H 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 3.37^([a]) I-047 chloro H 2-fluoro-3-methylsulfanylphenyl Ring 1 (2,4-dimethylphenyl)methyl 4.33^([a]) I-048 chloro H 2-fluoro-3-(trifluoromethoxy) Ring 1 (2,4-dimethylphenyl)methyl 4.61^([a]) phenyl I-049 chloro H 3-(trifluoromethyl)phenyl Ring 1 2,4-dichlorophenyl 4.30^([a]); 4.23^([b]) I-050 methyl H 3-cyclopropylphenyl Ring 1 (2,4-dimethylphenyl)methyl 3.90^([a]) I-051(*) chloro H 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.39^([a]) I-052(*) methyl H 3-cyclopropyl-2-fluorophenyl Ring 1 (2,4-dimethylphenyl)methyl 4.01^([)ª^(]) I-053(*) chloro H 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.39^([a]) I-054 methyl H 3-(trifluoromethyl)phenyl Ring 1 indan-5-yl 3.67^([a]) I-055(*) methyl methyl 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 3.63^([a]) I-056(*) methyl H 3-cyclopropyl-2-fluorophenyl Ring 1 (4-bromo-2-methylphenyl)methyl 4.12^([a]) I-057 methyl H 3-cyclopropyl-2-fluorophenyl Ring 1 (4-cyclopropyl-2-methylphenyl)methyl 4.28^([a]) I-058 chloro methyl 3-cyclopropyl-2-fluorophenyl Ring 1 (2,4-dimethylphenyl)methyl 4.30^([a]) I-059(*) chloro H 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.39^([a]) I-060 3-chloropyridin- H 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.37^([)ª^(]) 4-yl I-061 methyl H 3-(trifluoromethyl)phenyl Ring 1 4-methoxyphenyl 2.90^([a]) I-062 methyl H 3-(trifluoromethyl)phenyl Ring 3 1-methyl-1H-indol-5-yl 1.92^([a]) I-063 (1Z)-1- H 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.53^([a]) (methoxyimino) ethyl I-064 (1E)-1- H 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.96^([a]) (methoxyimino) ethyl I-065 chloro iodo 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.37^([a]) I-066 1-hydroxyethyl H 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 3.55^([a]) I-067 1-fluoroethyl H 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.30^([a]) I-068 cyclopropyl H 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.47^([a]) I-069 2- H 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 5.54^([a]) trimethylsilyl- ethyn-1-yl I-070(*) chloro H 3-(trifluoromethyl)phenyl Ring 1 benzyl 3.81^([a]) I-071 ethynyl H 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 3.59^([a]) I-072 chloro 2-methoxyethoxy 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.18^([a]) I-073 1H-imidazol- H 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 3.11^([a]) 1-yl I-074 methyl H 3-(trifluoromethyl)phenyl Ring 1 2-hydroxy-3,5-dimethylphenyl 3.01^([a]) I-075 methyl H 3-cyclopropyl-2-fluorophenyl Ring 1 (2-chloro-4-cyclopropylphenyl)methyl 4.39^([a]) I-076 chloro methyl 3-cyclopropyl-2-fluorophenyl Ring 1 (2,4-dichlorophenyl)methyl 4.51^([)ª^(]) I-077 chloro H 3-cyclopropylphenyl Ring 4 2,4-dimethylphenyl 4.11^([a]) I-078 chloro H 3-cyclopropylphenyl Ring 4 (2,4-dimethylphenyl)methyl 4.31^([a]) I-079 methyl H 3-(trifluoromethyl)phenyl Ring 3 (2,4-dichlorophenyl)methyl 3.97^([a]) I-080 methyl H 3-(trifluoromethyl)phenyl Ring 13 4-chlorophenyl 3.35^([a]) I-081 methyl H 3-(trifluoromethyl)phenyl Ring 12 4-chlorophenyl 3.45^([a]) I-082 chloro H 5-bromopyridin-3-yl Ring 1 (2,4-dimethylphenyl)methyl 3.67^([a]) I-083 chloro H 6-chloro-5-(trifluoromethyl) Ring 1 (2,4-dimethylphenyl)methyl 4.41^([a]) pyridin-3-yl I-084 chloro methyl 3-cyclopropyl-2-fluorophenyl Ring 1 (4-bromo-2-chlorophenyl)methyl 4.61^([a]) I-085 chloro methyl 3-cyclopropyl-2-fluorophenyl Ring 1 (2-chloro-4-cyclopropylphenyl)methyl 4.69^([a]) I-086 chloro H 3-cyclopropylphenyl Ring 1 (2,4-dimethylphenyl)methyl 4.53^([a]) I-087 methyl H 3-(trifluoromethyl)phenyl Ring 1 2,3-dihydro-1-benzofuran-5-yl 2.88^([a]) I-088 chloro pyridin-4-yl 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 3.76^([a]) I-089 vinyl H 3-cyclopropyl-2-fluorophenyl Ring 1 (2,4-dimethylphenyl)methyl 4.46^([a]) I-090 methyl H 3-(trifluoromethyl)phenyl Ring 1 2,5-dimethyl-3-thienyl 3.44^([a]) I-091 methyl H 3-(trifluoromethyl)phenyl Ring 1 5-methyl-2-thienyl 3.11^([a]) I-092 methyl H 3-(trifluoromethyl)phenyl Ring 1 1-methyl-1H-pyrrolo[2,3-b] 2.25^([a]) pyridin-3-yl I-093 methyl H 3-(trifluoromethyl)phenyl Ring 1 2-(4-chloro-2,6-difluorophenyl)ethyl 3.96^([a]) I-094 methyl H 3-(trifluoromethyl)phenyl Ring 1 (4-methylphenyl)methyl 3.58^([a]) I-095 methyl H 3-(trifluoromethyl)phenyl Ring 14 2,4-difluorophenyl 3.13^([a]) I-096 methyl H 3-(trifluoromethyl)phenyl Ring 15 2,4-dichlorophenyl 4.56^([a]) I-097 chloro H 5-(difluoromethyl)pyridin-3-yl Ring 1 (2,4-dimethylphenyl)methyl 3.42^([a]) I-098 1-ethoxyethen- H 3-cyclopropylphenyl Ring 1 (2,4-dimethylphenyl)methyl 5.11^([a]) 1-yl I-099 methyl H 3-(trifluoromethyl)phenyl Ring 1 5-chloro-2-thienyl 3.25^([a]) I-100 methyl H 3-(trifluoromethyl)phenyl Ring 1 5-methyl-2-furyl 2.92^([a]) I-101 methyl H 3-(trifluoromethyl)phenyl Ring 1 2,5-dimethyl-3-furyl 3.13^([a]) I-102 methyl H 3-(trifluoromethyl)phenyl Ring 1 4,5-dimethyl-2-furyl 3.21^([a]) I-103 methyl H 3-(trifluoromethyl)phenyl Ring 1 5-chloro-2-methyl-3-thienyl 3.57^([a]) I-104 methyl H 3-(trifluoromethyl)phenyl Ring 1 6-chloro-1-methyl-1H-indol-3-yl 3.57^([a]) I-105 methyl H 3-(trifluoromethyl)phenyl Ring 1 thiophen-2-yl 2.80^([a]) I-106 methyl H 3-(trifluoromethyl)phenyl Ring 1 1-benzothiophen-3-yl 3.44^([a]) I-107 methyl H 3-(trifluoromethyl)phenyl Ring 1 5-chloro-4-methyl-2-thienyl 3.62^([a]) I-108 pyrrolidin-1-yl H 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 3.37^([a]) I-109 vinyl H 3-cyclopropylphenyl Ring 1 (2,4-dimethylphenyl)methyl 4.36^([a]) I-110 ethyl H 3-cyclopropyl-2-fluorophenyl Ring 1 (2,4-dimethylphenyl)methyl 4.44^([a]) I-111 ethyl H 3-cyclopropylphenyl Ring 1 (2,4-dimethylphenyl)methyl 4.29^([a]) I-112 1-ethoxyethen- H 3-cyclopropyl-2-fluorophenyl Ring 1 (2,4-dimethylphenyl)methyl 5.27^([a]) 1-yl I-113 chloro H 2-fluoro-3-vinylphenyl Ring 1 (2,4-dimethylphenyl)methyl 4.46^([a]) I-114 methyl H 3-(trifluoromethyl)phenyl Ring 1 1-benzofuran-2-yl 3.31^([a]) I-115 methyl H 3-(trifluoromethyl)phenyl Ring 1 3-methyl-2-thienyl 3.11^([a]) I-116 methyl H 3-(trifluoromethyl)phenyl Ring 1 4-methyl-2-thienyl 3.15^([a]) I-117 chloro H 3-(trifluoromethyl)phenyl Ring 5 (2,4-dimethylphenyl)methyl 2.56^([a]) I-118 chloro H 3-cyclopropylphenyl Ring 5 (2,4-dimethylphenyl)methyl 2.41^([a]) I-119(*) methyl H 3-cyclopropyl-2-fluorophenyl Ring 1 (2,4-dimethylphenyl)methyl 4.12^([a]) I-120 acetyl H 3-cyclopropyl-2-fluorophenyl Ring 1 (2,4-dimethylphenyl)methyl 4.49^([a]) I-121 acetyl H 3-cyclopropylphenyl Ring 1 (2,4-dimethylphenyl)methyl 4.37^([a]) I-122 1-hydroxyethyl H 3-cyclopropyl-2-fluorophenyl Ring 1 (2,4-dimethylphenyl)methyl 3.70^([a]) I-123 chloro H 3-cyclopropylphenyl Ring 1 (2,4-dichlorophenyl)methyl 4.67^([a]) I-124 1-fluoroethyl H 3-cyclopropyl-2-fluorophenyl Ring 1 (2,4-dimethylphenyl)methyl 4.59^([a]) I-125 1-fluoroethyl H 3-cyclopropylphenyl Ring 1 (2,4-dimethylphenyl)methyl 4.46^([a]) I-126 methyl H 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methoxy 3.55^([a]) I-127 vinyl H 3-cyclopropylphenyl Ring 1 (2,4-dichlorophenyl)methyl 4.44^([a]) I-128 chloro methyl 5-(difluoromethyl)pyridin-3-yl Ring 1 (2,4-dimethylphenyl)methyl 3.21^([a]) I-129 ethyl H 3-cyclopropylphenyl Ring 1 (2,4-dichlorophenyl)methyl 4.37^([a]) I-130(*) methyl H 3-cyclopropyl-2-fluorophenyl Ring 1 (2,4-dimethylphenyl)methyl 4.12^([a]) I-131 methyl H 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)thio 3.92^([a]) I-132 methyl H 3-(trifluoromethyl)phenyl Ring 1 2-(2,4-dichlorophenyl)propan-2-yl 4.49^([a]) I-133 methyl H 3-(trifluoromethyl)phenyl Ring 1 2-(4-chlorophenyl)ethyl 3.72^([a]) I-134 methyl H 3-(trifluoromethyl)phenyl Ring 16 3,4-dichlorophenyl 4.80^([a]) I-135 methyl H 3-(trifluoromethyl)phenyl Ring 17 (4-chlorophenoxy)methyl 3.89^([a]) I-136 acetyl H 3-cyclopropylphenyl Ring 1 (2,4-dichlorophenyl)methyl 4.49^([a]) I-137 1-hydroxyethyl H 3-cyclopropylphenyl Ring 1 (2,4-dichlorophenyl)methyl 3.71^([a]) I-138 methyl H 3-cyclopropyl-2-fluorophenyl Ring 1 (2-methyl-4-vinylphenyl)methyl 4.08^([a]) I-139 methyl H 3-(trifluoromethyl)phenyl Ring 1 (4-chlorophenoxy)methyl 3.64^([a]) I-140 methyl H 3-cyclopropyl-2-fluorophenyl Ring 1 (2-methyl-4-pyridin-3-ylphenyl) 2.28^([a]) methyl I-141 1-fluoroethyl H 3-cyclopropylphenyl Ring 1 (2,4-dichlorophenyl)methyl 4.56^([a]) I-142 methyl H 3-cyclopropyl-2-fluorophenyl Ring 1 (4-ethynyl-2-methylphenyl)methyl 3.67^([a]) I-143 methyl H 3-(trifluoromethyl)phenyl Ring 6 4-chlorophenyl 3.50^([a]) I-144 methyl H 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenoxy)methyl 3.98^([a]) I-145(*) methyl methyl 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 3.71^([a]) I-146(*) methyl methyl 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 3.71^([a]) I-147 chloro H 3-cyclopropyl-2-fluorophenyl Ring 1 (2,4-dichlorophenyl)methyl 4.81^([a]) I-148 3-methyl- H 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 3.37^([a]) pyridin- 4-yl I-149 3- H 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 3.72^([a]) methoxy- pyridin- 4-yl I-150 pyridin-4-yl methyl 3-cyclopropyl-2-fluorophenyl Ring 1 (2,4-dimethylphenyl)methyl 3.29^([a]) I-151(*) chloro H 3-(trifluoromethyl)phenyl Ring 1 (2,4-dichlorophenyl)methyl 4.59^([a]) I-152(*) chloro H 3-(trifluoromethyl)phenyl Ring 1 (2,4-dichlorophenyl)methyl 4.59^([a]) I-153 chloro H 2-fluoro-3-[rac-2,2- Ring 1 (2,4-dimethylphenyl)methyl 4.37^([a]) difluorocyclopropyl]phenyl I-154 methyl H 3-(trifluoromethyl)phenyl Ring 7 4-methoxyphenyl 3.60^([a]) I-155 methyl H 2-fluoro-3-[rac-2,2- Ring 1 (2,4-dimethylphenyl)methyl 3.81^([a]) difluorocyclopropyl]phenyl I-156 chloro H 3-(trifluoromethyl)phenyl Ring 8 benzyl 2.72^([a]) I-157 iodo methyl 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.37^([a]) I-158 1,3-thiazol-5-yl H 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.18^([a]) I-159 cyano H 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.30^([a]) I-160(*) methyl H 3-(difluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 3.47^([a]) I-161(*) methyl H 3-(difluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 3.47^([a]) I-162(*) chloro H 3-(trifluoromethyl)phenyl Ring 1 (4-bromo-2-chlorophenyl)methyl 4.70^([a]) I-163(*) chloro H 3-(trifluoromethyl)phenyl Ring 1 (4-bromo-2-chlorophenyl)methyl 4.70^([a]) I-164(*) chloro H 3-(trifluoromethyl)phenyl Ring 1 (4-bromo-2-methylphenyl)methyl 4.59^([a]) I-165(*) chloro H 3-(trifluoromethyl)phenyl Ring 1 (4-bromo-2-methylphenyl)methyl 4.59^([a]) I-166(*) methyl H 3-(trifluoromethyl)phenyl Ring 1 1-methyl-1H-indol-3-yl 3.31^([a]) I-167(*) methyl H 3-(trifluoromethyl)phenyl Ring 1 1-methyl-1H-indol-3-yl 3.31^([a]) I-168 methyl H 3-(trifluoromethyl)phenyl Ring 1 3,5-dichloropyridin-2-yl 3.54^([a]) I-169 (cyclopropyl- methyl 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 3.84^([a]) amino)carbonyl I-170 vinyl H 3-cyclopropyl-2-fluorophenyl Ring 1 (2,4-dichlorophenyl)methyl 4.66^([a]) I-171 acetyl H 3-cyclopropyl-2-fluorophenyl Ring 1 (2,4-dichlorophenyl)methyl 4.66^([a]) I-172 ethyl H 3-cyclopropyl-2-fluorophenyl Ring 1 (2,4-dichlorophenyl)methyl 4.59^([a]) I-173 chloro H 3-(trifluoromethyl)phenyl Ring 8 (2,4-dimethylphenyl)methyl 3.31^([a]) I-174 chloro methyl 2-fluoro-3-[rac-2,2- Ring 1 (2,4-dimethylphenyl)methyl 4.15^([a]) difluorocyclopropyl]phenyl I-175 chloro H 3-(trifluoromethyl)phenyl Ring 1 [4-(trifluoromethyl)phenyl]methyl 4.23^([a]) I-176 methylsulfanyl methyl 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.51^([a]) I-177 4-methyl-1H- H 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.55^([a]) pyrazol-1-yl I-178 allylthio methyl 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 5.00^([a]) I-179 chloro H 3-(trifluoromethyl)phenyl Ring 1 [(2,4-dimethylphenyl)thio]methyl 4.78^([a]) I-180 methylsulfonyl methyl 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.01^([a]) I-181 chloro H 3-(trifluoromethyl)phenyl Ring 9 (2,4-dimethylphenyl)methyl 5.00^([a]) I-182 chloro H 3-(trifluoromethyl)phenyl Ring 10 (2,4-dimethylphenyl)methyl 5.61^([a]) I-183 chloro H 3-(trifluoromethyl)phenyl Ring 1 [4-(trifluoromethoxy)phenyl]methyl 4.40^([a]) I-184 chloro H 3-(trifluoromethyl)phenyl Ring 11 2,4-dichlorophenyl 3.88^([a]) I-185 chloro H 3-(trifluoromethyl)phenyl Ring 4 4-chlorophenyl 4.13^([a]) I-186 chloro H 3-chloro-2-fluorophenyl Ring 1 (2,4-dimethylphenyl)methyl 4.40^([a]) I-187 2- methyl 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.51^([a]) methoxy- ethylthio I-188 chloro H 3-(trifluoromethyl)phenyl Ring 1 [4-(difluoromethoxy)phenyl]methyl 3.88^([a]) I-189 vinyl H 3-chloro-2-fluorophenyl Ring 1 (2,4-dimethylphenyl)methyl 4.19^([a]) I-190 methyl H 3-chloro-2-fluorophenyl Ring 1 (2,4-dimethylphenyl)methyl 3.81^([a]) I-191 methoxy methyl 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 3.56^([a]) I-192 methyl H 3-cyclopropyl-2-fluorophenyl Ring 1 (4-cyclopentyl-2-methylphenyl) 5.28^([a]) methyl I-193 methyl H 3-cyclopropyl-2-fluorophenyl Ring 1 (4-cyclobutyl-2-methylphenyl) 4.97^([a]) methyl I-194 chloro H 3-(trifluoromethyl)phenyl Ring 4 2,4-dichlorophenyl 4.77^([a]) I-195 chloro H 3-(trifluoromethyl)phenyl Ring 11 4-chlorophenyl 3.56^([a]) I-196 chloro H 5-(trifluoromethyl)-3-thienyl Ring 1 (2,4-dimethylphenyl)methyl 4.59^([a]) I-197 chloro H 5-chloro-4-fluoropyridin-3-yl Ring 1 (2,4-dimethylphenyl)methyl 3.84^([a]) I-198 chloro H 5-cyclopropylpyridin-3-yl Ring 1 (2,4-dimethylphenyl)methyl 3.34^([a]) I-199 chloro H phenyl Ring 1 (2,4-dimethylphenyl)methyl 3.91^([a]) I-200 chloro H 3-methylphenyl Ring 1 (2,4-dimethylphenyl)methyl 4.26^([a]) I-201 chloro H 3-ethynylphenyl Ring 1 (2,4-dimethylphenyl)methyl 4.05^([a]) I-202 chloro H 3-formylphenyl Ring 1 (2,4-dimethylphenyl)methyl 3.47^([a]) I-203 chloro H 3-ethylphenyl Ring 1 (2,4-dimethylphenyl)methyl 4.59^([a]) I-204 chloro H 3-methoxyphenyl Ring 1 (2,4-dimethylphenyl)methyl 3.91^([a]) I-205 chloro H 2-fluoro-3-methylphenyl Ring 1 (2,4-dimethylphenyl)methyl 4.33^([a]) I-206 chloro H 1-isopropyl-1H-pyrazol-4-yl Ring 1 (2,4-dimethylphenyl)methyl 3.40^([a]) I-207 chloro H 2,3-difluorophenyl Ring 1 (2,4-dimethylphenyl)methyl 4.08^([a]) I-208 chloro H 1H-indol-5-yl Ring 1 (2,4-dimethylphenyl)methyl 3.57^([a]) I-209 chloro H indan-4-yl Ring 1 (2,4-dimethylphenyl)methyl 4.74^([a]) I-210 chloro H indan-5-yl Ring 1 (2,4-dimethylphenyl)methyl 4.78^([a]) I-211 chloro H 6,7-dihydro-5H- Ring 1 (2,4-dimethylphenyl)methyl 3.14^([a]) cyclopenta[b]pyridin-3-yl I-212 chloro H 2,3-dihydro-1-benzofuran-5-yl Ring 1 (2,4-dimethylphenyl)methyl 3.81^([a]) I-213 chloro H 3-acetylphenyl Ring 1 (2,4-dimethylphenyl)methyl 3.54^([a]) I-214 chloro H 3-propylphenyl Ring 1 (2,4-dimethylphenyl)methyl 5.00^([a]) I-215 chloro H 3-(dimethylamino)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.12^([a]) I-216 chloro H 3-ethoxyphenyl Ring 1 (2,4-dimethylphenyl)methyl 4.26^([a]) I-217 chloro H 3-(methoxymethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 3.87^([a]) I-218 chloro H 3-nitrophenyl Ring 1 (2,4-dimethylphenyl)methyl 3.84^([a]) I-219 chloro H 2-fluoro-3-formylphenyl Ring 1 (2,4-dimethylphenyl)methyl 3.64^([a]) I-220 chloro H 3-ethyl-2-fluorophenyl Ring 1 (2,4-dimethylphenyl)methyl 4.70^([a]) I-221 chloro H 3-methylsulfanylphenyl Ring 1 (2,4-dimethylphenyl)methyl 4.26^([a]) I-222 chloro H 3-chloro-4-methylphenyl Ring 1 (2,4-dimethylphenyl)methyl 4.70^([a]) I-223 chloro H naphthalen-2-yl Ring 1 (2,4-dimethylphenyl)methyl 4.51^([a]) I-224 chloro H quinolin-3-yl Ring 1 (2,4-dimethylphenyl)methyl 3.57^([a]) I-225 chloro H 3-chloro-5-fluorophenyl Ring 1 (2,4-dimethylphenyl)methyl 4.47^([a]) I-226 chloro H 3-chloro-4-fluorophenyl Ring 1 (2,4-dimethylphenyl)methyl 4.37^([a]) I-227 chloro H 2,4,5-trifluorophenyl Ring 1 (2,4-dimethylphenyl)methyl 4.19^([a]) I-228 chloro H 3-cyclobutylphenyl Ring 1 (2,4-dimethylphenyl)methyl 5.12^([a]) I-229 chloro H 3-(oxetan-3-yl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 3.47^([a]) I-230 chloro H 1-benzothiophen-6-yl Ring 1 (2,4-dimethylphenyl)methyl 4.33^([a]) I-231 chloro H 3-(methoxycarbonyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 3.84^([a]) I-232 chloro H 3-(2-fluorocyclopropyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.15 & 4.26^([a]) I-233 chloro H 4-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.44^([a]) I-234 chloro H 3,4-dichlorophenyl Ring 1 (2,4-dimethylphenyl)methyl 4.74^([a]) I-235 chloro H 3-phenylphenyl Ring 1 (2,4-dimethylphenyl)methyl 4.89^([a]) I-236 chloro H 3-bromophenyl Ring 1 (2,4-dimethylphenyl)methyl 4.40^([a]) I-237 chloro H 3-(trifluoromethoxy)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.59^([a]) I-238 chloro H 4-(trifluoromethoxy)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.59^([a]) I-239(*) chloro H 3-bromo-2-fluorophenyl Ring 1 (2,4-dimethylphenyl)methyl 4.47^([a]) I-240 chloro H 3-(trifluoromethylthio)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.85^([a]) I-241 chloro H 3-iodophenyl Ring 1 (2,4-dimethylphenyl)methyl 4.55^([a]) I-242 chloro H 3-[3-(trifluoromethyl)-1H- Ring 1 (2,4-dimethylphenyl)methyl 4.66^([a]) pyrazol-1-yl]phenyl I-243 chloro H 3-methylsulfonylphenyl Ring 1 (2,4-dimethylphenyl)methyl 3.13^([a]) I-244 chloro H 5-methyl-2-(trifluoromethyl)-1,3- Ring 1 (2,4-dimethylphenyl)methyl 4.40^([a]) thiazol-4-yl I-245(*) methyl H 3-cyclopropyl-2-fluorophenyl Ring 1 (2,4-dichlorophenyl)methyl 4.19^([a]) I-246(*) methyl H 3-cyclopropyl-2-fluorophenyl Ring 1 (4-bromo-2-chlorophenyl)methyl 4.30^([a]) I-247(*) methyl H 3-cyclopropyl-2-fluorophenyl Ring 1 (4-bromo-2-chlorophenyl)methyl 4.30^([a]) I-248 methyl H 3-cyclopropyl-2-fluorophenyl Ring 1 [2-methyl-4-(oxetan-3-yl) 3.13^([a]) phenyl]methyl I-249 methyl H 3-cyclopropyl-2-fluorophenyl Ring 1 [2-methyl-4-(oxolan-3-yl) 3.97^([a]) phenyl]methyl I-250(*) methyl H 3-cyclopropyl-2-fluorophenyl Ring 1 (2,4-dichlorophenyl)methyl 4.19^([a]) I-251 2-methoxyethyl methyl 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 3.85^([a]) I-252 ethyl H 3-chloro-2-fluorophenyl Ring 1 (2,4-dimethylphenyl)methyl 4.15^([a]) I-253 oxetan-3-yl H 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 3.77^([a]) I-254 2-methoxyethyl H 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.05^([a]) I-255 oxolan-3-yl H 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.01^([a]) I-256 2-cyanoethyl H 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.01^([a]) I-257 cyclobutyl- H 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 5.08^([a]) methyl I-258 chloro H 3-cyano-2-fluorophenyl Ring 1 (2,4-dimethylphenyl)methyl 3.77^([a]) I-259 methyl H 3-cyclopropyl-2-fluorophenyl Ring 1 (2-bromo-4-methylphenyl)methyl 4.26^([a]) I-260 chloro H 5-(trifluoromethyl)-3-thienyl Ring 1 (2,4-dichlorophenyl)methyl 4.66^([a]) I-261 chloro H 5-(trifluoromethyl)-3-thienyl Ring 1 (4-bromo-2-chlorophenyl)methyl 4.74^([a]) I-262 chloro H 2-fluoro-3-(1- Ring 1 (2,4-dimethylphenyl)methyl 4.44^([a]) fluorocyclopropyl)phenyl I-263 chloro methyl 2-fluoro-3-(1- Ring 1 (2,4-dimethylphenyl)methyl 4.19^([a]) fluorocyclopropyl)phenyl I-264 chloro 2-methoxyethyl 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.47^([a]) I-265 chloro cyclopentyl 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 5.20^([a]) I-266 chloro (4-methoxy-4- 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.05^([a]) oxobutyl)amino I-267 chloro (2-hydroxy-2- 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 3.88^([a]) methyl- propyl)amino I-268 chloro 5- 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 5.04^([a]) (trifluoromethyl)- 1H-pyrazol-1-yl I-269 chloro 3-carboxy- 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 3.40^([a]) propylamino I-270 chloro H 3-(trifluoromethyl)phenyl Ring 1 [4-(difluoromethyl)phenyl]methyl 3.48^([a]) I-271 chloro H 3-(difluoromethoxy)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.08^([a]) I-272 chloro H 2,2-difluoro-1,3- Ring 1 (2,4-dimethylphenyl)methyl 4.55^([a]) benzodioxol-5-yl I-273 methyl H 3-cyclopropyl-2-fluorophenyl Ring 1 [2-chloro-4- 4.26^([a]) (trifluoromethyl)phenyl]methyl I-274 chloro H 3-(trifluoromethyl)phenyl Ring 1 (1-methyl-1H-indol-3-yl)methyl 4.12^([a]) I-275 chloro H 3-bicyclo[4.2.0]octa-1,3,5- Ring 1 (2,4-dimethylphenyl)methyl 4.44^([a]) trienyl I-276 chloro H 3-(difluoromethoxy)-2- Ring 1 (2,4-dimethylphenyl)methyl 4.12^([a]) fluorophenyl I-277 2-cyclopropyl- H 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 5.20^([a]) cyclopropyl I-278 chloro 2-cyclopropyl- 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 5.16^([a]) cyclopropyl I-279 chloro allyloxy 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.67^([a]) I-280 chloro (2-methyl-1,3- 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.19^([a]) dioxolan-4- yl)methylamino I-281 chloro 2-oxopyrrolidin- 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.12^([a]) 1-yl I-282 chloro 2-oxa-6-aza- 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 3.71^([a]) spiro[3.3]heptan- 6-yl I-283 chloro (1-methylcyclo- 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.44^([a]) propyl)amino I-284 chloro 2-cyclopropyl- 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.74^([a]) ethylamino I-285 chloro but-3-en-2-yl- 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.55^([a]) amino I-286 chloro oxetan-3-ylamino 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 3.71^([a]) I-287 chloro 3,3,3-trifluoro- 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.51^([a]) propylamino I-288 chloro (2-cyclopropyl- 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.78^([a]) cyclopropyl)amino I-289 chloro 2-methylsulfanyl- 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.40^([a]) ethylamino I-290 methyl H 3-cyclopropyl-2-fluorophenyl Ring 1 (2-chloro-4-methylphenyl)methyl 4.12^([a]) I-291 chloro 3-(oxolan-2-yl)- 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.55^([a]) 1H-pyrazol-1-yl I-292 chloro methylsulfanyl 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.51^([a]) I-293 4-methoxy-1H- 4-methoxy-1H- 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.40^([a]) pyrazol-1-yl pyrazol-1-yl I-294 chloro 1,3-thiazol-4-yl 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.17^([a]) I-295 methyl H 3-cyclopropyl-2-fluorophenyl Ring 1 (3,4-dichlorophenyl)methyl 4.08^([a]) I-296 chloro H 3-(trifluoromethyl)phenyl Ring 1 (4-nitrophenyl)methyl 3.54^([a]) I-297 chloro H 3-(trifluoromethyl)phenyl Ring 1 [4-(trifluoromethylthio)phenyl]methyl 4.67^([a]) I-298 methyl H 3-chloro-2-fluorophenyl Ring 1 (2-chloro-4-cyclopropylphenyl)methyl 4.14^([a]) I-299 methyl H 3-chloro-2-fluorophenyl Ring 1 (4-cyclopropyl-2-methylphenyl)methyl 4.12^([a]) I-300(*) methyl H 3-chloro-2-fluorophenyl Ring 1 (4-bromo-2-methylphenyl)methyl 3.94^([a]) I-301 methyl H 3-cyclopropyl-2-fluorophenyl Ring 1 (2-chloro-4-methoxyphenyl)methyl 3.73^([a]) I-302(*) methyl H 3-chloro-2-fluorophenyl Ring 1 (2-chloro-4-methylphenyl)methyl 3.94^([a]) I-303 methyl H 3-chloro-2-fluorophenyl Ring 1 (3,4-dimethylphenyl)methyl 3.87^([a]) I-304 chloro H 3-(trifluoromethyl)phenyl Ring 5 2,4-dichlorophenyl 2.76^([a]) I-305 methyl H 3-(difluoromethyl)phenyl Ring 1 (3,4-dimethylphenyl)methyl 3.46^([a]) I-306 methyl H 3-(difluoromethyl)phenyl Ring 1 (4-cyclopropyl-2-methylphenyl)methyl 3.72^([a]) I-307 chloro H 3-(trifluoromethyl)phenyl Ring 1 (5-chloropyridin-2-yl)methyl 3.43^([a]) I-308 chloro H 3-ethynyl-2-fluorophenyl Ring 1 (2,4-dichlorophenyl)methyl 4.16^([a]) I-309 methyl H 3-cyclopropyl-2-fluorophenyl Ring 1 (3-bromo-5-methylphenyl)methyl 4.26^([a]) I-310 chloro H 3-(trifluoromethyl)phenyl Ring 1 (4,5-dimethyl-3-thienyl)methyl 4.36^([a]) I-311 methyl H 3-(trifluoromethyl)phenyl Ring 1 2-phenylcyclopropyl 3.57^([a]) I-312(*) chloro H 3-bromo-2-fluorophenyl Ring 1 (2,4-dimethylphenyl)methyl 4.51^([a]) I-313(*) chloro H 3-bromo-2-fluorophenyl Ring 1 (2,4-dimethylphenyl)methyl 4.51^([a]) I-314 methyl H 3-cyclopropyl-2-fluorophenyl Ring 1 [4-methyl-2-(2-trimethylsilylethyn-1- 5.79^([a]) yl)phenyl]methyl I-315 methyl H 3-cyclopropyl-2-fluorophenyl Ring 1 (2-ethynyl-4-methylphenyl)methyl 3.88^([a]) I-316 methyl H 3-(difluoromethyl)-2- Ring 1 (2,4-dimethylphenyl)methyl 3.59^([a]) fluorophenyl I-317 methyl H 3-(difluoromethyl)-2- Ring 1 (3,4-dimethylphenyl)methyl 3.62^([a]) fluorophenyl I-318 methyl H 3-(trifluoromethyl)phenyl Ring 1 2,3-dihydro-1,4-benzodioxin-6-yl 2.89^([a]) I-319 chloro H 3-[rac-oxiran-2-yl]phenyl Ring 1 (2,4-dichlorophenyl)methyl 3.84^([a]) I-320 chloro 2-methoxy- 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.52^([a]) ethylthio I-321 chloro H 3-ethynyl-2-fluorophenyl Ring 1 (2,4-dimethylphenyl)methyl 4.17^([a]) I-322(*) methyl H 3-cyclopropyl-2-fluorophenyl Ring 1 (4-bromo-2-methylphenyl)methyl 4.23^([a]) I-323(*) methyl H 3-cyclopropyl-2-fluorophenyl Ring 1 (4-bromo-2-methylphenyl)methyl 4.23^([a]) I-324 methyl H 3-(difluoromethyl)-2- Ring 1 (4-cyclopropyl-2-methylphenyl)methyl 3.88^([a]) fluorophenyl I-325 methyl H 2-fluoro-3-vinylphenyl Ring 1 (2,4-dimethylphenyl)methyl 3.88^([a]) I-326 methyl H 2-fluoro-3-methylphenyl Ring 1 (2,4-dimethylphenyl)methyl 3.70^([a]) I-327 methyl H 3-cyclopropylphenyl Ring 1 (2-chloro-4-cyclopropylphenyl)methyl 4.36^([a]) I-328 methyl H 3-cyclopropylphenyl Ring 1 (4-cyclopropyl-2-methylphenyl)methyl 4.19^([a]) I-329 methyl H 3-cyclopropylphenyl Ring 1 (4-bromo-2-methylphenyl)methyl 4.03^([a]) I-330 methyl H 3-cyclopropylphenyl Ring 1 (3,4-dimethylphenyl)methyl 3.93^([a]) I-331 methyl H 3-cyclopropyl-2-fluorophenyl Ring 1 [2-chloro-4-(difluoro- 3.73^([a]) methyl)phenyl]methyl I-332 methyl H 3-cyclopropyl-2-fluorophenyl Ring 1 [2-chloro-4-(difluoro- 3.81^([a]) methoxy)phenyl]methyl I-333 methyl H 3-(difluoromethyl)phenyl Ring 1 (2-chloro-4-methylphenyl)methyl 3.49^([a]) I-334 methyl H 3-cyclopropyl-2-fluorophenyl Ring 1 [2-chloro-4-(trifluoro- 4.41^([a]) methoxy)phenyl]methyl I-335 methyl H 3-cyclopropyl-2-fluorophenyl Ring 1 (2-cyclopropyl-4-methylphenyl)methyl 4.51^([a]) I-336(*) methyl H 3-chloro-2-fluorophenyl Ring 1 (4-bromo-2-methylphenyl)methyl 3.94^([a]) I-337(*) methyl H 3-chloro-2-fluorophenyl Ring 1 (4-bromo-2-methylphenyl)methyl 3.94^([a]) I-338(*) methyl H 3-chloro-2-fluorophenyl Ring 1 (2-chloro-4-methylphenyl)methyl 3.87^([a]) I-339(*) methyl H 3-chloro-2-fluorophenyl Ring 1 (2-chloro-4-methylphenyl)methyl 3.87^([a]) I-340 chloro H 6-chloropyridin-2-yl Ring 1 (2,4-dichlorophenyl)methyl 3.77^([a]) I-341 chloro H 3-vinylphenyl Ring 1 (2,4-dichlorophenyl)methyl 4.44^([a]) I-342 chloro 4-methoxy-1H- 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.35^([a]) pyrazol-1-yl I-343 chloro cyclopropyl 3-(trifluoromethyl)phenyl Ring 1 (2,4-dimethylphenyl)methyl 4.46^([a]) I-344 methyl H 3-(difluoromethyl)-2- Ring 1 (2-chloro-4-methylphenyl)methyl 3.63^([a]) fluorophenyl I-345 methyl H 2-fluoro-3-formylphenyl Ring 1 (2,4-dimethylphenyl)methyl 3.09^([a]) I-346 methyl H 3-cyclopropylphenyl Ring 1 (2-chloro-4-methylphenyl)methyl 3.96^([a]) I-347 chloro H 3-(trifluoromethyl)phenyl Ring 1 (E)-2-phenylethen-1-yl 3.91^([a]) I-348 methyl H 3-ethynyl-2-fluorophenyl Ring 1 (2,4-dimethylphenyl)methyl 3.52^([a]) (*)Ex I-051 and I-053 are the two enantiomers of Ex I-059 Ex I-051: Optical rotation: +92.7° (c = 0.95, DCM, 25° C.); concentration c is expressed in g/100 mL. Ex I-053: Optical rotation: −86.6° (c = 1.04, DCM, 25° C.); concentration c is expressed in g/100 mL. (*)Ex I-119 and I-130 are the 2 enantiomers of Ex I-052 Ex I-119: Optical rotation: +95.3° (c = 1.05, CDCl3, 20° C.); concentration c is expressed in g/100 mL. Ex I-130: Optical rotation: −93.3° (c = 1.20, CDCl3, 20° C.); concentration c is expressed in g/100 mL. (*)Ex I-145 and I-146 are the 2 enantiomers of Ex I-055 Ex I-145: Optical rotation: +86.3° (c = 1.62, CDCl3, 20° C.); concentration c is expressed in g/100 mL. Ex I-146: Optical rotation: −90° (c = 1.60, CDCl3, 20° C.); concentration c is expressed in g/100 mL. (*)Ex I-151 and I-152 are the 2 enantiomers of Ex I-025 Ex I-151: Optical rotation: +54.8° (c = 1.1, CDCl3, 25° C.); concentration c is expressed in g/100 mL. Ex I-152: Optical rotation: −51.4° (c = 1.09, CDCl3, 25° C.); concentration c is expressed in g/100 mL. (*)Ex I-160 and I-161 are the 2 enantiomers of Ex I-013 Ex I-160: Optical rotation: +85.6° (c = 2.15, CDCl3, 25° C.); concentration c is expressed in g/100 mL. Ex I-161: Optical rotation: −78.1° (c = 2.15, CDCl3, 25° C.); concentration c is expressed in g/100 mL. (*)Ex I-162 and I-163 are the 2 enantiomers of Ex I-016 Ex I-162: Optical rotation: +52.2° (c = 1.15, CDCl3, 25° C.); concentration c is expressed in g/100 mL. Ex I-163: Optical rotation: −72° (c = 1.0, CDCl3, 25° C.); concentration c is expressed in g/100 mL. (*)Ex I-164 and I-165 are the 2 enantiomers of Ex I-017 Ex I-164: Optical rotation: +78.3° (c = 1.15, CDCl3, 25° C.); concentration c is expressed in g/100 mL. Ex I-165: Optical rotation: −85.5° (c = 1.1, CDCl3, 25° C.); concentration c is expressed in g/100 mL. (*)Ex I-166 and I-167 are the 2 enantiomers of Ex I-011 Ex I-166: Optical rotation: 0° (c = 0.95, CDCl3, 25° C.); concentration c is expressed in g/100 mL. Ex I-167: Optical rotation: −7.3° (c = 1.1, CDCl3, 25°C); concentration c is expressed in g/100 mL. (*)Ex I-245 and I-250 are the 2 enantiomers of Ex I-030 Ex I-245: Optical rotation: +57.1° (c = 0.67, CDCl3, 25° C.); concentration c is expressed in g/100 mL. Ex I-250: Optical rotation: −63.8° (c = 0.69, CDCl3, 25° C.); concentration c is expressed in g/100 mL. (*)Ex I-246 and I-247 are the 2 enantiomers of Ex I-027 Ex I-246: Optical rotation: +60° (c = 0.6, CDCl3, 25° C.); concentration c is expressed in g/100 mL. Ex I-247: Optical rotation: −55° (c = 0.8, CDCl3, 25° C.); concentration c is expressed in g/100 mL. (*)Ex I-312 and I-313 are the 2 enantiomers of Ex I-239 Ex I-312: Optical rotation: −88.6° (c = 3.50, DCM, 20° C.); concentration c is expressed in g/100 mL. Ex I-313: Optical rotation: +73.2° (c = 2.95, DCM, 20° C.); concentration c is expressed in g/100 mL. (*)Ex I-322 and I-323 are the 2 enantiomers of Ex I-056 (*)Ex I-336 and I-337 are the 2 enantiomers of Ex I-300 Ex I-336: Optical rotation: +71.6° (c = 1.01, CDCl3, 25° C.); concentration c is expressed in g/100 mL. Ex I-337: Optical rotation: −72.5° (c = 1.02, CDCl3, 25° C.); concentration c is expressed in g/100 mL. (*)Ex I-338 and I-339 are the 2 enantiomers of Ex I-302 Ex I-338: Optical rotation: +71.5° (c = 1.04, CDCl3, 25° C.); concentration c is expressed in g/100 mL. Ex I-339: Optical rotation: −75.2° (c = 1.01, CDCl3, 25° C.); concentration c is expressed in g/100 mL. (*)Ex I-070 is Single Stereoisomer Ex I-070: Optical rotation: −78.1° (c = 2.51, CDCl3, 25° C.); concentration c is expressed in g/100 mL.

TABLE 2 I-001: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1367 (6.2); 7.2983 (14.2); 7.1511 (0.6); 7.1469 (0.6); 7.1244 (1.4); 7.1206 (1.4); 7.0979 (1.0); 7.0941 (1.0); 7.0120 (2.6); 6.9870 (3.2); 6.9609 (0.6); 6.9557 (0.6); 6.9061 (2.1); 6.8920 (0.9); 6.8868 (0.8); 6.8649 (1.3); 6.8434 (0.6); 6.8386 (0.6); 6.6980 (1.2); 6.6728 (1.0); 6.2039 (1.4); 5.3372 (8.7); 4.3108 (0.7); 4.3024 (1.0); 4.2776 (1.1); 4.2677 (0.9); 3.9014 (0.6); 3.8854 (0.6); 3.8792 (0.5); 3.8620 (2.1); 3.8417 (0.6); 3.8275 (1.4); 3.8068 (0.8); 3.0515 (0.7); 3.0359 (0.7); 3.0069 (1.0); 2.9905 (1.0); 2.7798 (0.9); 2.7488 (0.9); 2.7346 (0.8); 2.7033 (0.7); 2.3087 (11.5); 2.1735 (10.9); 2.1492 (0.6); 2.1373 (0.6); 2.1204 (1.0); 2.1032 (0.6); 2.0921 (0.6); 2.0830 (1.5); 1.5870 (16.0); 1.3455 (0.4); 1.3211 (1.0); 1.3053 (2.5); 1.2976 (2.7); 1.2736 (0.5); 1.1084 (0.7); 1.0953 (1.4); 1.0884 (1.8); 1.0831 (1.1); 1.0802 (1.1); 1.0753 (1.1); 1.0665 (1.4); 1.0601 (1.7); 1.0472 (0.9); 0.9420 (0.8); 0.9203 (2.6); 0.8972 (1.1); 0.8445 (0.8); 0.8369 (0.9); 0.8279 (1.9); 0.8203 (1.6); 0.8124 (2.0); 0.8052 (1.2); 0.7949 (0.7); 0.1077 (3.9); 0.0489 (0.4); 0.0381 (12.7); 0.0272 (0.6) I-002: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.5046 (0.5); 7.4888 (2.4); 7.4771 (5.7); 7.4754 (5.5); 7.3398 (6.4); 7.2616 (4.9); 7.2520 (3.1); 7.1885 (1.0); 7.1827 (1.7); 7.1783 (1.6); 7.1702 (1.5); 7.1659 (1.0); 6.9515 (2.6); 6.9363 (3.0); 6.8897 (3.3); 6.7050 (1.8); 6.6901 (1.6); 6.1002 (2.2); 4.7630 (1.1); 4.7533 (1.2); 4.2173 (1.3); 4.2108 (1.5); 4.1958 (1.5); 4.1893 (1.6); 3.8515 (0.7); 3.8475 (0.7); 3.8417 (0.9); 3.8381 (0.9); 3.8319 (1.0); 3.8285 (0.9); 3.8249 (0.8); 3.8227 (0.8); 3.8122 (0.4); 3.7817 (2.0); 3.7692 (1.4); 3.7602 (1.8); 3.7476 (1.4); 2.9828 (8.6); 2.9727 (9.1); 2.9600 (1.6); 2.9503 (1.4); 2.9323 (1.5); 2.9228 (1.4); 2.7000 (1.5); 2.6804 (1.5); 2.6727 (1.4); 2.6529 (1.2); 2.6119 (12.8); 2.2491 (16.0); 2.1702 (15.0); 1.2548 (0.8); 0.8463 (0.4); 0.0712 (1.2); −0.0002 (5.3) I-003: ¹H-NMR(400.0 MHz, d₆-DMSO): δ = 8.0691 (16.0); 7.7706 (1.0); 7.7504 (3.4); 7.7303 (3.6); 7.7152 (4.4); 7.7016 (5.9); 7.6184 (2.8); 7.5984 (2.1); 7.4089 (3.5); 7.4013 (3.3); 7.2721 (7.1); 7.2511 (10.1); 7.1570 (11.0); 7.1361 (7.7); 5.7549 (6.2); 4.0558 (0.5); 4.0380 (1.6); 4.0202 (1.7); 4.0024 (0.6); 3.8298 (1.1); 3.8230 (2.0); 3.7994 (4.4); 3.7725 (2.0); 3.7605 (3.2); 3.7534 (1.9); 3.7365 (1.8); 3.7284 (0.8); 3.3217 (129.8); 2.8669 (0.5); 2.8538 (0.6); 2.8337 (2.9); 2.8215 (4.4); 2.8054 (2.6); 2.7907 (0.6); 2.7712 (0.5); 2.6753 (0.8); 2.6709 (1.0); 2.6663 (0.8); 2.6619 (0.4); 2.5240 (3.1); 2.5106 (63.6); 2.5063 (131.0); 2.5018 (174.2); 2.4973 (124.7); 2.4929 (59.8); 2.3331 (0.7); 2.3285 (1.0); 2.3241 (0.7); 2.0739 (3.3); 1.9886 (7.0); 1.3358 (0.4); 1.2983 (0.7); 1.2587 (1.1); 1.2346 (2.6); 1.1928 (2.2); 1.1750 (4.2); 1.1572 (2.1); 0.9404 (0.4); 0.9235 (0.4); 0.8534 (0.4); 0.0077 (0.6); −0.0003 (17.2); −0.0084 (0.6) I-004: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.9364 (5.2); 7.5605 (0.6); 7.5473 (1.0); 7.5342 (0.6); 7.4162 (0.5); 7.4138 (0.5); 7.3999 (1.1); 7.3861 (0.7); 7.3837 (0.6); 7.3215 (0.9); 7.3054 (1.3); 7.2893 (0.5); 7.2598 (4.4); 6.9781 (1.8); 6.9628 (2.0); 6.8688 (2.0); 6.6891 (1.1); 6.6741 (1.0); 6.0251 (1.2); 4.2657 (0.9); 4.2592 (1.0); 4.2442 (1.0); 4.2377 (1.0); 3.8922 (0.4); 3.8876 (0.4); 3.8818 (0.6); 3.8780 (0.5); 3.8721 (0.6); 3.8684 (0.5); 3.8655 (0.4); 3.8623 (0.4); 3.8302 (1.6); 3.8179 (1.0); 3.8087 (1.4); 3.7963 (1.0); 2.9979 (0.8); 2.9881 (0.8); 2.9706 (1.0); 2.9607 (0.9); 2.7425 (1.1); 2.7230 (1.1); 2.7152 (0.9); 2.6956 (0.9); 2.6411 (16.0); 2.2708 (11.4); 2.1118 (10.6); −0.0002 (5.4) I-005: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.0849 (8.6); 7.9524 (1.3); 7.4247 (1.5); 7.4167 (1.5); 7.2527 (0.5); 7.2484 (0.5); 7.2317 (1.4); 7.2276 (1.4); 7.2108 (1.1); 7.2070 (1.2); 7.1790 (0.9); 7.1751 (1.0); 7.1570 (1.4); 7.1390 (0.6); 7.1354 (0.5); 7.0574 (2.0); 7.0382 (2.4); 6.9707 (0.8); 6.9667 (0.9); 6.9537 (1.0); 6.9504 (1.5); 6.9466 (1.0); 6.9334 (3.1); 6.8353 (1.3); 6.8165 (1.1); 3.9038 (16.0); 3.7795 (0.3); 3.7611 (1.5); 3.7519 (3.0); 3.7482 (2.9); 3.7361 (0.7); 3.7264 (1.1); 3.7208 (0.9); 3.7084 (0.6); 3.6996 (0.4); 3.3316 (26.0); 2.8906 (9.7); 2.8112 (1.2); 2.7965 (2.0); 2.7804 (1.3); 2.7316 (8.4); 2.5249 (0.6); 2.5201 (0.8); 2.5114 (9.7); 2.5070 (19.6); 2.5025 (25.9); 2.4979 (19.2); 2.4934 (9.5); 2.2409 (11.6); 2.1940 (10.6); −0.0002 (5.1) I-006: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.3681 (1.0); 7.3416 (2.4); 7.3147 (1.8); 7.2998 (5.3); 7.2987 (5.2); 7.2380 (1.8); 7.2349 (1.8); 7.2048 (2.2); 7.1972 (2.7); 7.1910 (1.4); 7.1157 (1.3); 7.1113 (1.2); 7.0883 (1.0); 7.0847 (1.0); 7.0424 (2.7); 7.0212 (0.8); 6.9957 (3.7); 6.9854 (2.6); 6.9592 (0.6); 5.3371 (2.7); 5.3360 (2.6); 4.9524 (1.6); 4.2431 (16.0); 4.1684 (0.4); 4.1582 (0.9); 4.1461 (1.2); 4.1217 (1.2); 4.1102 (1.2); 3.9416 (0.5); 3.9328 (0.6); 3.9224 (0.7); 3.9135 (0.8); 3.9037 (0.7); 3.8945 (0.5); 3.8849 (0.4); 3.8417 (1.5); 3.8229 (1.0); 3.8052 (1.1); 3.7864 (0.9); 3.0132 (0.7); 2.9936 (0.7); 2.9671 (1.2); 2.9475 (1.1); 2.8402 (1.2); 2.8118 (1.1); 2.7942 (0.8); 2.7657 (0.7); 2.6456 (0.4); 2.5162 (15.1); 2.3298 (12.2); 2.3104 (13.5); 2.1655 (0.8); 2.0810 (1.2); 2.0433 (5.2); 2.0422 (5.1); 1.6617 (1.1); 1.3203 (0.4); 1.2952 (1.2); 1.2731 (0.6); 0.8981 (0.5); 0.8766 (0.6); 0.1081 (0.7); 0.0380 (5.1); 0.0368 (5.0) I-007: ¹H-NMR(499.9 MHz, d₆-DMSO): δ = 8.1831 (16.0); 8.1727 (0.4); 8.1431 (8.2); 7.7474 (6.8); 7.7330 (4.5); 7.7171 (3.9); 7.6924 (4.7); 7.6769 (2.4); 7.6446 (3.4); 7.6284 (2.5); 7.5820 (6.9); 7.5777 (7.3); 7.4682 (3.6); 7.4517 (4.4); 7.3128 (2.7); 7.3093 (2.8); 7.2965 (2.3); 7.2930 (2.3); 4.3091 (1.2); 3.7162 (1.2); 3.5268 (0.9); 3.3395 (6.1); 3.0209 (2.1); 3.0071 (2.1); 2.9934 (2.9); 2.9797 (2.8); 2.8882 (2.8); 2.8746 (2.9); 2.8608 (2.1); 2.8471 (2.0); 2.6402 (0.7); 2.6366 (0.9); 2.6330 (0.8); 2.5231 (2.8); 2.5195 (3.6); 2.5053 (81.5); 2.5017 (113.2); 2.4982 (87.2); 2.3664 (0.6); 2.3628 (0.8); 2.3593 (0.6) I-008: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.6575 (6.0); 7.5545 (0.4); 7.5258 (2.8); 7.5083 (5.3); 7.2989 (10.6); 7.2789 (2.8); 7.2264 (0.3); 7.2119 (1.0); 7.1998 (1.4); 7.1931 (1.4); 7.1819 (1.1); 7.1740 (0.8); 6.9976 (2.5); 6.9722 (3.0); 6.9358 (3.2); 6.7594 (1.8); 6.7339 (1.5); 6.1087 (2.1); 5.3656 (2.2); 5.3375 (0.6); 4.2843 (1.2); 4.2745 (1.4); 4.2495 (1.5); 4.2400 (1.4); 3.8933 (0.8); 3.8766 (0.9); 3.8683 (0.7); 3.8608 (0.8); 3.8446 (2.6); 3.8238 (0.9); 3.8099 (1.8); 3.7889 (1.1); 3.0177 (1.0); 3.0031 (1.0); 2.9725 (1.4); 2.9571 (1.3); 2.7530 (1.4); 2.7214 (1.3); 2.7080 (1.1); 2.6757 (1.0); 2.6232 (0.9); 2.6111 (1.2); 2.6036 (0.9); 2.3343 (0.5); 2.3261 (0.4); 2.2904 (16.0); 2.2529 (0.5); 2.2179 (15.0); 1.7901 (0.8); 1.2916 (0.8); 0.9108 (0.6); 0.8898 (3.1); 0.8734 (3.2); 0.8683 (2.8); 0.8527 (0.9); 0.6339 (0.9); 0.6189 (2.8); 0.6109 (3.2); 0.6009 (2.6); 0.5845 (0.8); 0.1074 (1.3); 0.0373 (11.6) I-009: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.4299 (6.8); 7.6093 (4.4); 7.5923 (4.4); 7.5654 (0.3); 7.3649 (2.6); 7.3138 (1.1); 7.2989 (10.8); 7.2760 (0.7); 7.0123 (2.5); 6.9868 (2.9); 6.9249 (3.1); 6.7230 (1.7); 6.6994 (1.4); 6.0943 (2.1); 5.5674 (3.4); 5.5594 (3.5); 5.3373 (0.8); 4.4552 (3.1); 4.4472 (3.2); 4.3387 (1.1); 4.3290 (1.4); 4.3041 (1.5); 4.2949 (1.4); 4.0408 (1.4); 4.0176 (4.4); 3.9943 (4.5); 3.9709 (1.6); 3.9480 (0.6); 3.9313 (0.8); 3.9151 (0.8); 3.9065 (0.7); 3.8992 (0.8); 3.8865 (2.7); 3.8659 (0.8); 3.8522 (1.8); 3.8312 (1.1); 3.0565 (1.0); 3.0426 (1.0); 3.0115 (1.4); 2.9963 (1.3); 2.7774 (1.3); 2.7456 (1.3); 2.7323 (1.1); 2.6998 (1.0); 2.3049 (16.0); 2.2389 (0.4); 2.1940 (14.9); 1.5999 (14.5); 1.4943 (4.7); 1.4710 (9.8); 1.4478 (4.6); 1.4067 (0.4); 1.3835 (0.4); 1.3610 (0.6); 1.3333 (0.5); 1.3069 (1.1); 0.9852 (0.6); 0.9610 (1.2); 0.9369 (0.7); 0.9201 (0.8); 0.8968 (0.4); 0.1087 (1.2); 0.0485 (0.4); 0.0382 (10.6) I-010: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.3149 (0.5); 8.0160 (1.7); 8.0061 (1.7); 7.8968 (6.8); 7.7408 (0.6); 7.7215 (1.8); 7.7004 (3.4); 7.6683 (3.9); 7.6630 (5.1); 7.6385 (2.1); 7.6175 (0.9); 7.6131 (0.9); 7.5242 (2.5); 7.5031 (3.3); 7.3900 (2.0); 7.3847 (1.9); 7.3690 (1.5); 7.3637 (1.4); 5.7548 (8.8); 5.0826 (0.6); 5.0741 (1.5); 5.0647 (1.5); 5.0558 (0.6); 4.0399 (0.9); 4.0314 (1.0); 4.0119 (1.5); 4.0035 (1.3); 3.9015 (1.2); 3.8933 (1.2); 3.8734 (0.9); 3.8650 (1.0); 3.3216 (143.7); 2.6751 (1.2); 2.6705 (1.7); 2.6660 (1.2); 2.6615 (0.6); 2.6263 (16.0); 2.5241 (5.2); 2.5192 (8.1); 2.5106 (99.3); 2.5061 (195.0); 2.5016 (253.0); 2.4970 (184.0); 2.4925 (90.1); 2.3375 (0.6); 2.3330 (1.2); 2.3284 (1.6); 2.3239 (1.2); 2.3195 (0.6); 2.0737 (0.3); 1.2352 (0.5); 0.8761 (0.4); 0.1460 (1.4); 0.1168 (3.2); 0.0899 (2.2); 0.0610 (2.0); 0.0080 (11.2); −0.0001 (308.4); −0.0084 (12.5); −0.1496 (1.4) I-011: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.9822 (5.1); 7.6532 (2.2); 7.6372 (2.1); 7.5021 (0.5); 7.4859 (2.9); 7.4759 (4.8); 7.3538 (2.8); 7.3316 (2.4); 7.3159 (3.8); 7.2585 (9.4); 7.2423 (1.9); 7.2272 (1.0); 7.0797 (4.9); 7.0568 (1.4); 7.0411 (2.1); 7.0267 (1.1); 6.1856 (2.1); 5.0888 (1.1); 5.0808 (1.2); 5.0732 (1.2); 5.0649 (1.0); 4.4325 (1.2); 4.4242 (1.2); 4.4105 (1.3); 4.4022 (1.2); 4.0366 (1.5); 4.0202 (1.6); 4.0147 (1.4); 3.9983 (1.2); 3.7438 (16.0); 2.6947 (15.5); 2.0428 (1.2); 1.5564 (2.7); 1.2723 (0.5); 1.2579 (0.9); 1.2437 (0.3); 0.0701 (0.6); −0.0002 (10.2) I-012: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.0009 (6.4); 7.5966 (4.6); 7.5798 (4.1); 7.5534 (0.3); 7.3519 (2.7); 7.2997 (14.2); 7.2981 (13.5); 7.2789 (1.4); 7.2726 (1.2); 7.2657 (1.0); 7.2574 (0.7); 7.0046 (2.5); 6.9790 (2.9); 6.9209 (3.1); 6.7152 (1.7); 6.6901 (1.4); 6.1644 (2.0); 4.3314 (1.2); 4.3213 (1.4); 4.2964 (1.5); 4.2863 (1.5); 4.1721 (0.9); 4.1483 (0.9); 4.1242 (0.4); 3.9181 (0.8); 3.9058 (0.9); 3.8987 (0.7); 3.8890 (0.7); 3.8818 (0.6); 3.8661 (2.3); 3.8450 (1.0); 3.8313 (1.8); 3.8101 (1.1); 3.0521 (1.1); 3.0377 (1.2); 3.0246 (1.6); 2.9992 (5.2); 2.9739 (4.9); 2.9485 (1.7); 2.7618 (1.4); 2.7295 (1.4); 2.7167 (1.2); 2.6837 (1.1); 2.3006 (16.0); 2.1898 (14.9); 2.0843 (4.1); 1.6221 (0.7); 1.3974 (5.0); 1.3725 (10.0); 1.3715 (9.9); 1.3470 (4.9); 1.3222 (1.2); 1.2967 (3.0); 1.2745 (1.2); 0.1082 (0.7); 0.0479 (0.6); 0.0386 (16.4); 0.0370 (15.8) I-013: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.9380 (5.2); 7.5220 (0.8); 7.5063 (1.8); 7.4904 (1.2); 7.4267 (1.6); 7.4113 (1.1); 7.2610 (11.8); 7.2063 (2.1); 7.1461 (1.1); 7.1439 (1.1); 7.1299 (1.1); 7.1276 (1.0); 6.9597 (2.0); 6.9444 (2.2); 6.8873 (2.4); 6.7791 (1.1); 6.6850 (1.3); 6.6665 (3.0); 6.5535 (1.1); 6.1534 (1.5); 5.2986 (7.8); 4.2586 (1.0); 4.2522 (1.1); 4.2371 (1.1); 4.2307 (1.2); 3.8749 (0.4); 3.8709 (0.5); 3.8654 (0.6); 3.8614 (0.6); 3.8552 (0.7); 3.8481 (0.5); 3.8455 (0.5); 3.8071 (1.6); 3.7945 (1.1); 3.7855 (1.4); 3.7729 (1.1); 2.9894 (0.8); 2.9800 (0.9); 2.9620 (1.0); 2.9526 (1.0); 2.7114 (1.1); 2.6916 (1.1); 2.6840 (1.0); 2.6642 (0.9); 2.6367 (16.0); 2.2594 (12.2); 2.1649 (11.5); 2.0445 (1.3); 1.5820 (9.2); 1.2586 (0.9); 1.2555 (0.9); 1.2446 (0.3); 0.9357 (0.4); 0.0062 (0.4); −0.0002 (11.4) I-014: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.2582 (3.2); 7.6116 (2.1); 7.5949 (1.7); 7.3622 (1.2); 7.2987 (8.5); 7.2881 (0.8); 7.2814 (0.6); 7.2679 (0.3); 7.0348 (0.7); 7.0072 (1.2); 6.9982 (0.9); 6.9815 (1.4); 6.9387 (0.9); 6.9231 (1.5); 6.7145 (0.8); 6.6896 (0.7); 6.2641 (1.5); 6.2049 (1.3); 6.1586 (1.0); 5.6878 (1.4); 5.6509 (1.4); 4.3449 (0.5); 4.3347 (0.6); 4.3096 (0.7); 4.2995 (0.7); 3.9299 (0.4); 3.9146 (0.4); 3.8985 (0.3); 3.8914 (0.3); 3.8778 (1.1); 3.8570 (0.4); 3.8430 (0.8); 3.8219 (0.5); 3.0604 (0.5); 3.0462 (0.5); 3.0154 (0.6); 2.9999 (0.6); 2.7673 (0.6); 2.7349 (0.6); 2.7221 (0.6); 2.6891 (0.5); 2.3039 (7.3); 2.1892 (6.9); 2.0834 (0.5); 1.6029 (16.0); 1.2973 (0.9); 0.9193 (0.6); 0.1070 (0.8); 0.0480 (0.3); 0.0372 (7.7) I-015: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.0398 (5.2); 7.9135 (1.8); 7.8942 (1.1); 7.8851 (2.7); 7.8628 (3.4); 7.7663 (0.9); 7.7483 (0.9); 7.7351 (1.1); 7.5838 (1.5); 7.5693 (2.0); 7.5644 (4.1); 7.5611 (4.1); 7.5538 (2.2); 7.5501 (2.4); 7.5356 (3.4); 7.5260 (3.2); 7.5030 (1.7); 7.4971 (1.5); 7.4744 (1.4); 7.4686 (1.4); 7.4634 (1.0); 7.4522 (1.2); 7.4448 (1.0); 7.4320 (0.8); 7.4238 (0.4); 7.2989 (15.3); 6.3678 (1.4); 4.9973 (0.6); 4.9882 (0.7); 4.9818 (0.8); 4.9732 (0.7); 4.9646 (0.6); 4.4812 (0.8); 4.4697 (0.8); 4.4441 (1.0); 4.4328 (0.9); 4.1707 (0.4); 4.1473 (0.4); 4.1240 (0.4); 4.1022 (0.6); 3.9204 (1.4); 3.8962 (1.4); 3.8834 (1.3); 3.8591 (1.2); 2.7518 (16.0); 2.0828 (3.6); 1.6711 (0.4); 1.6490 (0.5); 1.6402 (0.5); 1.6011 (1.3); 1.3444 (0.3); 1.3208 (0.8); 1.2940 (2.8); 1.2732 (0.7); 0.9980 (0.5); 0.9736 (1.0); 0.9492 (0.4); 0.9191 (0.4); 0.1089 (1.0); 0.0495 (0.6); 0.0387 (18.3); 0.0278 (0.8) I-016: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1593 (8.5); 7.6555 (4.0); 7.6382 (5.0); 7.4904 (3.5); 7.4847 (3.6); 7.4149 (2.3); 7.3157 (0.9); 7.2987 (17.1); 7.2855 (1.1); 7.2769 (0.8); 7.1496 (1.0); 7.1436 (0.9); 7.1225 (3.4); 7.1164 (3.6); 7.1015 (5.3); 7.0744 (1.4); 6.0646 (1.5); 5.3375 (2.2); 4.2023 (1.2); 4.1925 (1.5); 4.1666 (1.8); 4.1565 (2.0); 4.0578 (0.6); 4.0472 (0.8); 4.0306 (0.9); 4.0184 (1.0); 4.0087 (0.6); 4.0012 (0.6); 3.9914 (0.4); 3.9757 (2.2); 3.9600 (1.3); 3.9398 (1.5); 3.9242 (1.1); 3.1762 (1.1); 3.1589 (1.1); 3.1311 (1.9); 3.1136 (1.8); 3.0183 (1.9); 2.9887 (1.8); 2.9734 (1.2); 2.9435 (1.1); 2.0823 (1.1); 1.5867 (16.0); 1.2968 (0.7); 0.1076 (3.9); 0.0488 (0.7); 0.0379 (19.0); 0.0269 (0.7) I-017: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1640 (8.3); 7.6566 (3.3); 7.6519 (2.1); 7.6393 (4.9); 7.3917 (2.2); 7.2985 (14.8); 7.2564 (3.3); 7.2501 (3.5); 7.2432 (1.7); 7.2366 (1.3); 7.2270 (1.0); 7.2187 (0.7); 7.0563 (0.9); 7.0500 (0.8); 7.0293 (2.1); 7.0228 (2.2); 6.9936 (4.2); 6.9666 (1.6); 6.0785 (1.6); 5.3374 (2.7); 4.2585 (1.4); 4.2329 (1.7); 4.2136 (0.4); 3.9344 (0.5); 3.9249 (0.6); 3.9160 (0.9); 3.9019 (2.1); 3.8870 (0.9); 3.8724 (2.1); 3.8541 (0.8); 3.0382 (0.9); 3.0230 (0.9); 2.9926 (1.4); 2.9768 (1.3); 2.8220 (1.2); 2.7909 (1.2); 2.7766 (0.9); 2.7448 (0.8); 2.3204 (16.0); 2.0827 (1.2); 1.5830 (9.2); 1.2971 (0.5); 0.1078 (0.6); 0.0487 (0.7); 0.0381 (19.4); 0.0270 (0.6) I-018: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.0009 (5.2); 7.6148 (0.5); 7.5891 (1.7); 7.5671 (4.8); 7.5460 (0.5); 7.4934 (2.6); 7.4568 (1.0); 7.4492 (1.6); 7.4425 (1.1); 7.4265 (1.1); 7.3003 (11.0); 7.1857 (1.3); 7.1596 (3.3); 7.1476 (3.3); 7.1277 (2.2); 7.0992 (0.9); 6.1870 (1.9); 5.3393 (5.2); 4.7514 (0.9); 4.7380 (1.0); 4.7269 (1.0); 4.7124 (1.0); 4.3916 (1.2); 4.3777 (1.1); 4.3549 (1.3); 4.3409 (1.2); 3.7520 (1.5); 3.7260 (1.4); 3.7152 (1.4); 3.6893 (1.3); 2.7564 (0.4); 2.7335 (16.0); 2.3486 (0.4); 2.3228 (0.4); 2.2834 (13.3); 2.2222 (13.1); 2.1877 (0.3); 2.0844 (1.4); 1.6154 (4.2); 1.3223 (0.5); 1.2985 (1.0); 1.2748 (0.4); 0.1092 (3.2); 0.0392 (14.1) I-019: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1622 (8.7); 7.6504 (0.4); 7.6394 (4.7); 7.6362 (4.7); 7.6288 (2.0); 7.6243 (2.1); 7.6182 (2.5); 7.5917 (0.4); 7.3989 (2.3); 7.2987 (14.6); 7.2847 (1.0); 7.2761 (1.2); 7.2641 (1.3); 7.2574 (1.2); 7.2460 (0.7); 6.9900 (2.6); 6.9641 (3.0); 6.8192 (2.8); 6.5891 (1.6); 6.5835 (1.6); 6.5634 (1.4); 6.5577 (1.4); 6.1172 (1.9); 4.3289 (1.0); 4.3202 (1.3); 4.2942 (1.4); 4.2857 (1.2); 3.9179 (0.5); 3.9019 (0.7); 3.8915 (0.6); 3.8851 (0.8); 3.8760 (0.6); 3.8689 (0.8); 3.8596 (2.7); 3.8390 (0.8); 3.8252 (1.9); 3.8043 (1.1); 3.0504 (1.0); 3.0364 (1.0); 3.0053 (1.4); 2.9902 (1.3); 2.7430 (1.2); 2.7108 (1.2); 2.6978 (1.2); 2.6650 (1.0); 2.2999 (16.0); 1.7742 (0.3); 1.7572 (0.7); 1.7459 (0.8); 1.7292 (1.5); 1.7123 (0.9); 1.7011 (0.9); 1.6841 (0.6); 1.6521 (5.5); 0.9521 (0.5); 0.9359 (2.4); 0.9295 (2.7); 0.9135 (1.2); 0.9077 (2.5); 0.9014 (2.4); 0.8857 (0.6); 0.5647 (1.0); 0.5576 (1.3); 0.5485 (2.0); 0.5417 (2.6); 0.5349 (2.2); 0.5251 (1.5); 0.5185 (1.1); 0.1077 (1.3); 0.0485 (0.5); 0.0377 (16.0); 0.0268 (0.6) I-020: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.2759 (0.5); 8.1614 (16.0); 7.6511 (0.9); 7.6402 (8.7); 7.6374 (8.0); 7.6284 (4.0); 7.6230 (5.9); 7.5938 (0.6); 7.4169 (4.4); 7.3341 (1.8); 7.3250 (2.1); 7.3151 (2.8); 7.3088 (2.4); 7.2986 (16.3); 7.0801 (5.7); 7.0540 (6.4); 7.0100 (6.5); 7.0041 (6.8); 6.9887 (0.3); 6.6804 (3.7); 6.6744 (3.7); 6.6543 (3.2); 6.6483 (3.2); 6.1040 (3.1); 4.2671 (2.3); 4.2564 (2.6); 4.2310 (2.9); 4.2203 (3.1); 4.0577 (0.4); 4.0473 (0.6); 4.0396 (1.0); 4.0305 (1.3); 4.0233 (1.3); 4.0153 (1.4); 4.0083 (1.4); 3.9999 (1.4); 3.9921 (1.1); 3.9833 (0.9); 3.9733 (0.5); 3.9182 (3.8); 3.8998 (2.7); 3.8820 (3.1); 3.8636 (2.4); 3.1723 (2.1); 3.1564 (2.1); 3.1272 (3.1); 3.1113 (2.9); 2.9287 (3.1); 2.8975 (3.0); 2.8837 (2.3); 2.8524 (2.1); 2.0819 (1.0); 2.0438 (0.9); 1.7885 (0.7); 1.7717 (1.3); 1.7605 (1.4); 1.7437 (2.8); 1.7269 (1.6); 1.7158 (1.5); 1.6988 (0.8); 1.5983 (12.6); 1.2964 (0.5); 0.9968 (0.9); 0.9792 (4.5); 0.9733 (5.2); 0.9700 (4.3); 0.9512 (4.7); 0.9453 (4.5); 0.9283 (1.0); 0.9101 (0.3); 0.6107 (0.5); 0.6020 (0.4); 0.5935 (0.6); 0.5795 (2.9); 0.5757 (2.4); 0.5703 (2.3); 0.5632 (4.7); 0.5578 (4.4); 0.5543 (4.2); 0.5474 (2.3); 0.5399 (2.6); 0.5267 (0.5); 0.5224 (0.5); 0.5160 (0.4); 0.5056 (0.4); 0.0477 (0.6); 0.0371 (19.6); 0.0261 (0.7) I-021: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1713 (12.5); 7.6375 (6.4); 7.6343 (6.6); 7.6261 (3.0); 7.6208 (3.8); 7.6172 (4.1); 7.5906 (0.6); 7.4428 (3.3); 7.3555 (1.3); 7.3470 (1.7); 7.3364 (2.0); 7.3298 (1.7); 7.3257 (1.3); 7.3169 (1.0); 7.2989 (19.2); 7.1958 (4.5); 7.1902 (4.8); 7.1358 (4.1); 7.1098 (4.8); 6.8484 (2.6); 6.8428 (2.6); 6.8224 (2.2); 6.8168 (2.2); 6.1296 (2.4); 5.3379 (0.4); 4.2733 (1.7); 4.2626 (2.0); 4.2372 (2.2); 4.2265 (2.4); 4.0481 (0.7); 4.0327 (1.0); 4.0244 (1.1); 4.0174 (1.0); 4.0086 (1.1); 4.0012 (0.8); 3.9929 (0.7); 3.9823 (0.4); 3.9344 (2.9); 3.9160 (2.0); 3.8983 (2.3); 3.8798 (1.7); 3.1899 (1.6); 3.1744 (1.6); 3.1450 (2.3); 3.1293 (2.2); 2.9467 (2.4); 2.9156 (2.2); 2.9019 (1.8); 2.8705 (1.6); 2.8134 (0.6); 2.7907 (1.5); 2.7678 (2.1); 2.7448 (1.6); 2.7216 (0.7); 1.6106 (4.4); 1.2911 (0.4); 1.2434 (0.5); 1.2203 (0.6); 1.1628 (15.5); 1.1543 (16.0); 1.1397 (15.5); 1.1313 (15.5); 0.9294 (0.4); 0.9052 (0.7); 0.1074 (1.8); 0.0482 (0.7); 0.0374 (21.2); 0.0265 (0.8) I-022: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1556 (4.2); 7.6218 (2.2); 7.6188 (2.6); 7.6093 (0.9); 7.5989 (1.2); 7.3483 (1.2); 7.2987 (8.7); 7.2672 (0.5); 7.2595 (0.7); 7.2454 (0.6); 7.2380 (0.7); 7.2287 (0.4); 6.9673 (1.6); 6.8960 (1.8); 6.8897 (3.2); 6.1298 (0.9); 5.3372 (1.8); 4.3501 (0.6); 4.3400 (0.6); 4.3143 (0.7); 4.3038 (0.7); 4.1714 (1.0); 4.1476 (1.0); 4.1239 (0.4); 3.9270 (0.4); 3.9223 (0.4); 3.9164 (0.4); 3.9108 (0.3); 3.9054 (0.4); 3.8250 (1.2); 3.8029 (0.7); 3.7891 (1.0); 3.7670 (0.7); 3.0294 (0.5); 3.0140 (0.5); 2.9845 (0.7); 2.9690 (0.6); 2.6547 (0.8); 2.6217 (0.8); 2.6098 (0.7); 2.5765 (0.6); 2.1286 (7.9); 2.1021 (8.1); 2.0826 (5.0); 2.0440 (1.3); 1.5959 (16.0); 1.3208 (1.2); 1.2970 (2.4); 1.2732 (1.1); 0.1076 (1.9); 0.0378 (9.7); 0.0269 (0.4) I-023: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1706 (8.2); 7.6486 (0.3); 7.6360 (4.0); 7.6328 (4.6); 7.6272 (1.9); 7.6226 (1.8); 7.6134 (2.2); 7.5870 (0.4); 7.4230 (2.1); 7.3165 (0.9); 7.3089 (1.3); 7.2987 (12.3); 7.2883 (1.4); 7.2784 (0.7); 7.0377 (2.3); 7.0119 (2.8); 6.9867 (2.7); 6.7625 (1.5); 6.7569 (1.5); 6.7367 (1.3); 6.7312 (1.3); 6.1531 (1.7); 4.3309 (0.9); 4.3222 (1.2); 4.2963 (1.3); 4.2876 (1.1); 4.1947 (0.9); 4.1708 (2.7); 4.1470 (2.8); 4.1233 (1.0); 3.9274 (0.5); 3.9144 (0.6); 3.9064 (0.6); 3.8952 (0.7); 3.8854 (0.6); 3.8716 (2.5); 3.8511 (0.6); 3.8373 (1.8); 3.8164 (1.0); 3.0636 (0.9); 3.0500 (0.9); 3.0183 (1.4); 3.0038 (1.3); 2.7925 (0.4); 2.7691 (1.1); 2.7576 (1.3); 2.7462 (1.5); 2.7243 (2.0); 2.7121 (1.2); 2.7007 (0.5); 2.6795 (1.0); 2.3677 (0.5); 2.3298 (14.7); 2.0830 (12.3); 1.6012 (16.0); 1.3210 (3.2); 1.2972 (6.5); 1.2839 (0.4); 1.2734 (3.2); 1.2609 (0.3); 1.2227 (0.6); 1.1997 (0.6); 1.1621 (10.2); 1.1526 (10.5); 1.1391 (10.2); 1.1296 (10.2); 0.1077 (1.1); 0.0484 (0.4); 0.0376 (12.9); 0.0266 (0.5) I-024: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.1176 (8.0); 7.5773 (0.7); 7.5655 (1.3); 7.5518 (0.8); 7.3426 (0.8); 7.3266 (2.1); 7.3108 (1.9); 7.3032 (1.1); 7.2999 (1.2); 7.2874 (1.4); 7.2716 (0.6); 7.2601 (7.6); 6.9914 (1.4); 6.9602 (2.5); 6.9449 (2.7); 6.8819 (2.9); 6.8645 (2.8); 6.7724 (1.4); 6.6673 (1.5); 6.6523 (1.3); 6.0266 (1.7); 4.2866 (1.3); 4.2802 (1.3); 4.2651 (1.4); 4.2585 (1.4); 3.8865 (0.6); 3.8824 (0.6); 3.8788 (0.8); 3.8765 (0.8); 3.8727 (0.7); 3.8665 (0.8); 3.8629 (0.6); 3.8597 (0.6); 3.8567 (0.6); 3.8530 (0.4); 3.8226 (2.1); 3.8101 (1.3); 3.8011 (1.8); 3.7886 (1.3); 3.0078 (1.1); 2.9981 (1.1); 2.9805 (1.3); 2.9708 (1.2); 2.7181 (1.4); 2.6983 (1.4); 2.6908 (1.2); 2.6710 (1.1); 2.2663 (15.0); 2.1374 (0.3); 2.1112 (14.0); 2.0035 (16.0); 1.5659 (3.3); 0.0062 (0.5); −0.0002 (7.6) I-025: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1610 (3.5); 7.6500 (1.9); 7.6327 (1.8); 7.4041 (1.0); 7.3372 (1.5); 7.3302 (1.6); 7.3194 (0.4); 7.3107 (0.5); 7.2987 (8.3); 7.2807 (0.3); 7.1690 (1.2); 7.1417 (1.6); 6.9965 (1.0); 6.9894 (1.0); 6.9693 (0.7); 6.9622 (0.7); 6.0661 (0.6); 5.3373 (2.4); 4.2068 (0.5); 4.1966 (0.6); 4.1707 (0.8); 4.1608 (0.8); 4.0501 (0.3); 4.0331 (0.4); 4.0217 (0.4); 3.9754 (0.9); 3.9597 (0.6); 3.9396 (0.6); 3.9238 (0.5); 3.1899 (0.4); 3.1726 (0.4); 3.1448 (0.8); 3.1274 (0.7); 3.0286 (0.8); 2.9989 (0.7); 2.9836 (0.5); 2.9536 (0.4); 2.0820 (0.5); 1.5923 (16.0); 1.3452 (0.4); 1.3202 (0.8); 1.3045 (2.3); 1.2974 (2.1); 0.9414 (0.8); 0.9197 (2.5); 0.8964 (1.0); 0.1073 (2.3); 0.0376 (9.0); 0.0267 (0.3) I-026: ¹H-NMR(300.1 MHz, CDCl3): δ = 7.6924 (5.4); 7.5036 (0.4); 7.4781 (2.0); 7.4678 (2.2); 7.4585 (4.7); 7.3058 (3.2); 7.2842 (1.6); 7.2645 (1.1); 7.1899 (3.9); 7.1099 (6.2); 7.0966 (6.2); 7.0421 (1.3); 7.0293 (1.4); 7.0105 (0.7); 5.2336 (1.4); 5.1971 (1.4); 5.1334 (1.9); 4.3992 (0.5); 4.3898 (0.6); 4.3753 (0.7); 4.3654 (0.8); 4.3586 (0.9); 4.3489 (0.9); 4.3345 (0.9); 4.3250 (0.8); 4.1797 (0.6); 4.1558 (0.9); 4.1503 (0.9); 4.1390 (0.6); 4.1263 (0.8); 4.1149 (0.7); 4.1093 (0.7); 4.0853 (0.5); 2.7381 (0.4); 2.7328 (0.4); 2.7270 (0.4); 2.7144 (0.5); 2.7088 (0.5); 2.7021 (0.5); 2.6907 (0.6); 2.6852 (0.6); 2.6786 (0.6); 2.6726 (0.5); 2.6604 (0.5); 2.6543 (0.5); 2.6492 (0.5); 2.6242 (0.4); 2.5767 (16.0); 2.1486 (0.7); 2.1251 (0.8); 2.1163 (0.8); 2.0887 (14.0); 1.9181 (0.4); 1.7135 (0.4); −0.0008 (1.9); −0.0762 (1.4) I-027: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.8980 (5.4); 7.4723 (3.2); 7.4687 (3.1); 7.2638 (1.8); 7.1046 (1.0); 7.0886 (2.3); 7.0828 (2.2); 7.0723 (1.9); 7.0665 (3.8); 7.0414 (2.5); 7.0378 (2.4); 7.0249 (2.1); 7.0101 (1.6); 6.9962 (0.8); 6.9936 (0.7); 6.8242 (1.0); 6.8220 (1.0); 6.8089 (1.6); 6.7954 (0.8); 6.1646 (1.7); 4.1371 (1.3); 4.1308 (1.4); 4.1153 (1.6); 4.1090 (1.5); 4.0015 (0.4); 3.9921 (0.7); 3.9856 (1.0); 3.9767 (1.0); 3.9682 (1.0); 3.9586 (0.6); 3.9207 (1.6); 3.9115 (1.2); 3.8989 (1.3); 3.8897 (1.0); 3.1377 (1.1); 3.1277 (1.1); 3.1108 (1.4); 3.1007 (1.3); 2.9453 (1.4); 2.9270 (1.4); 2.9184 (1.1); 2.9000 (1.0); 2.6365 (16.0); 2.1019 (0.4); 2.0915 (0.7); 2.0848 (0.8); 2.0747 (1.2); 2.0645 (0.8); 2.0579 (0.7); 1.6411 (1.0); 1.0409 (0.7); 1.0316 (2.3); 1.0282 (2.4); 1.0256 (2.0); 1.0147 (2.3); 1.0113 (2.2); 1.0022 (0.5); 0.8031 (0.4); 0.7996 (0.4); 0.7862 (1.7); 0.7804 (1.6); 0.7763 (2.4); 0.7732 (2.4); 0.7711 (2.4); 0.7609 (1.4); −0.0002 (2.4) I-028: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9768 (4.5); 7.5997 (0.6); 7.5735 (1.4); 7.5470 (1.0); 7.4838 (1.2); 7.4579 (0.7); 7.3462 (2.3); 7.3392 (2.4); 7.2989 (10.5); 7.2770 (1.5); 7.2251 (0.8); 7.2218 (0.9); 7.2178 (0.8); 7.1950 (0.8); 7.1910 (0.7); 7.1625 (1.9); 7.1352 (2.4); 6.9665 (1.5); 6.9594 (1.5); 6.9393 (1.2); 6.9322 (1.1); 6.9082 (1.0); 6.7205 (1.9); 6.5327 (1.0); 6.1544 (0.9); 5.3374 (9.2); 4.1905 (0.8); 4.1803 (0.9); 4.1703 (0.4); 4.1546 (1.1); 4.1447 (1.4); 4.0373 (0.5); 4.0212 (0.5); 4.0082 (0.6); 3.9985 (0.4); 3.9912 (0.4); 3.9599 (1.4); 3.9442 (0.8); 3.9241 (0.9); 3.9083 (0.7); 3.1856 (0.7); 3.1684 (0.7); 3.1406 (1.1); 3.1233 (1.0); 3.0109 (1.1); 2.9810 (1.1); 2.9658 (0.7); 2.9358 (0.7); 2.6888 (14.2); 2.0824 (1.4); 1.6051 (16.0); 1.3203 (0.4); 1.2965 (0.8); 1.2727 (0.3); 0.1066 (1.8); 0.0478 (0.4); 0.0369 (11.6); 0.0258 (0.4) I-029: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.9706 (2.5); 7.8850 (4.3); 7.5588 (0.4); 7.5433 (1.4); 7.5274 (1.9); 7.5215 (2.1); 7.5062 (0.6); 7.4720 (1.9); 7.4249 (1.2); 7.4098 (0.9); 7.3756 (2.3); 7.2823 (0.9); 6.4695 (1.2); 6.3671 (1.0); 6.3607 (1.8); 6.3572 (1.8); 6.3387 (2.3); 6.3322 (1.6); 4.8737 (0.5); 4.8668 (0.8); 4.8613 (1.2); 4.8555 (0.9); 4.8490 (0.6); 4.3114 (0.9); 4.3036 (1.0); 4.2894 (1.1); 4.2816 (1.1); 4.0395 (1.2); 4.0269 (1.2); 4.0176 (1.1); 4.0050 (1.0); 2.9393 (16.0); 2.8554 (14.8); 2.6614 (13.0); 1.9093 (0.6); −0.0002 (1.0) I-030: ¹H-NMR(400.1 MHz, d₆-DMSO): δ = 7.7353 (16.0); 7.5384 (10.0); 7.4019 (7.4); 7.3811 (9.6); 7.3707 (6.9); 7.3622 (6.5); 7.1722 (6.9); 7.1555 (9.0); 7.1377 (9.8); 7.1163 (5.2); 7.0971 (1.8); 6.9317 (2.9); 6.9171 (5.2); 6.8983 (2.7); 5.7597 (1.1); 3.8638 (5.8); 3.8416 (9.8); 3.7722 (3.6); 3.7641 (5.0); 3.7435 (3.5); 3.3131 (22.3); 3.0449 (1.4); 3.0255 (1.6); 3.0111 (5.0); 2.9910 (7.5); 2.9735 (4.7); 2.9544 (1.6); 2.9395 (1.3); 2.5789 (43.3); 2.5101 (13.6); 2.1043 (1.0); 2.0910 (2.1); 2.0826 (2.6); 2.0706 (3.9); 2.0586 (2.6); 2.0505 (2.2); 2.0369 (1.0); 1.0606 (0.4); 1.0464 (2.4); 1.0323 (8.3); 1.0119 (8.0); 1.0008 (2.7); 0.8415 (0.4); 0.8282 (0.4); 0.8031 (3.1); 0.7909 (10.3); 0.7789 (9.7); 0.7661 (2.4) I-031: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.0083 (5.3); 7.5863 (1.3); 7.5644 (4.0); 7.5427 (0.4); 7.4936 (1.9); 7.4536 (0.9); 7.4451 (1.5); 7.4379 (1.1); 7.4211 (2.4); 7.4066 (13.7); 7.3887 (0.8); 7.3803 (0.7); 7.2986 (8.3); 6.2693 (1.2); 4.8288 (0.6); 4.8235 (0.6); 4.8155 (0.7); 4.8096 (0.8); 4.8053 (0.8); 4.7993 (0.7); 4.7913 (0.7); 4.7859 (0.7); 4.4019 (0.9); 4.3907 (0.8); 4.3672 (1.0); 4.3650 (1.0); 4.3537 (0.9); 3.8252 (1.5); 3.8010 (1.4); 3.7883 (1.4); 3.7641 (1.3); 2.7339 (16.0); 1.6570 (0.4); 1.2937 (0.6); 0.1086 (0.8); 0.0381 (7.9) I-032: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9905 (5.3); 7.6025 (3.3); 7.5856 (3.9); 7.4362 (2.1); 7.3449 (0.8); 7.3371 (0.9); 7.3295 (1.2); 7.3237 (1.1); 7.3146 (0.9); 7.2999 (9.6); 7.2028 (2.7); 7.1979 (2.8); 7.1412 (2.3); 7.1152 (2.6); 6.8417 (1.5); 6.8364 (1.5); 6.8158 (1.3); 6.8106 (1.3); 6.1569 (1.5); 4.2561 (1.0); 4.2453 (1.1); 4.2201 (1.3); 4.2093 (1.4); 4.0222 (0.7); 4.0153 (0.7); 4.0077 (0.7); 3.9283 (1.6); 3.9100 (1.1); 3.8922 (1.2); 3.8738 (1.0); 3.1875 (0.9); 3.1718 (0.9); 3.1423 (1.3); 3.1267 (1.2); 2.9446 (1.3); 2.9135 (1.3); 2.8996 (1.0); 2.8685 (0.9); 2.8195 (0.4); 2.8102 (0.5); 2.7968 (0.9); 2.7739 (1.4); 2.7507 (1.0); 2.7277 (0.4); 2.6854 (16.0); 1.6057 (9.2); 1.3031 (1.3); 1.2613 (0.5); 1.1696 (8.4); 1.1618 (8.8); 1.1466 (8.4); 1.1388 (8.4); 0.9344 (0.6); 0.9198 (1.1); 0.9100 (0.6); 0.8965 (0.5); 0.0383 (11.8) I-033: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.0987 (3.8); 7.4527 (1.0); 7.4487 (1.3); 7.4444 (0.9); 7.4400 (0.7); 7.4233 (1.2); 7.4074 (0.9); 7.2604 (4.6); 7.2091 (0.5); 7.1955 (0.7); 7.1819 (0.5); 7.0428 (0.4); 7.0265 (1.5); 7.0212 (2.2); 7.0172 (1.4); 7.0011 (0.3); 6.9678 (0.7); 6.9635 (1.0); 6.9564 (0.8); 6.9512 (0.7); 6.9463 (1.0); 6.1527 (0.7); 5.2965 (16.0); 4.1433 (0.4); 4.1396 (0.4); 4.1372 (0.4); 4.1335 (0.4); 4.1215 (0.4); 4.1176 (0.6); 4.1154 (0.6); 4.1117 (0.5); 3.9788 (0.4); 3.9693 (0.4); 3.9611 (0.4); 3.9066 (0.6); 3.8971 (0.5); 3.8850 (0.5); 3.8755 (0.4); 3.1203 (0.5); 3.1100 (0.5); 3.0932 (0.7); 3.0829 (0.7); 2.9325 (0.5); 2.9297 (0.5); 2.9143 (0.5); 2.9114 (0.5); 2.9055 (0.4); 2.9026 (0.4); 2.8872 (0.4); 2.8843 (0.4); 2.8017 (0.4); 2.7858 (0.5); 2.7769 (0.4); 2.7609 (0.4); 2.2960 (0.4); 1.8918 (0.4); 1.8768 (0.4); 1.8673 (0.5); 1.6558 (0.3); 1.6476 (0.4); 1.6439 (0.4); 1.6388 (0.4); 1.6350 (0.4); 1.6305 (0.5); 1.6266 (0.4); 1.6224 (0.4); 1.6186 (0.4); 1.6142 (0.4); 1.6103 (0.3); 1.6063 (0.4); 1.6024 (0.4); 1.5862 (0.5); 1.2919 (0.3); 1.2555 (1.3); 1.2396 (0.4); 0.8810 (0.3); 0.8453 (0.4); 0.8382 (0.4); 0.8331 (0.4); −0.0002 (5.4) I-034: ¹H-NMR(300.2 MHz, d₆-DMSO): δ =7.7819 (0.6); 7.7562 (1.8); 7.7302 (2.1); 7.7118 (2.6); 7.6863 (1.1); 7.6251 (3.1); 7.5836 (1.4); 7.4295 (2.1); 7.0467 (1.9); 7.0212 (2.4); 6.9600 (3.0); 6.8484 (1.8); 6.8237 (1.4); 3.8068 (5.6); 3.7715 (1.2); 3.3540 (16.0); 2.8234 (2.8); 2.8043 (2.7); 2.5226 (2.7); 2.4553 (12.2); 2.2395 (12.4); 2.2208 (12.0); 2.0099 (0.8); 1.2521 (0.4); 1.1954 (0.4) I-035: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9894 (5.2); 7.5999 (3.6); 7.5970 (3.2); 7.5827 (2.9); 7.4150 (1.9); 7.2993 (10.4); 7.2869 (1.3); 7.2807 (1.2); 7.2666 (0.6); 7.0522 (2.0); 7.0264 (2.4); 6.9910 (2.4); 6.7809 (1.3); 6.7757 (1.4); 6.7555 (1.1); 6.7505 (1.1); 6.1794 (1.6); 4.3094 (0.8); 4.3001 (1.1); 4.2745 (1.1); 4.2659 (1.0); 3.9279 (0.5); 3.9096 (0.7); 3.8957 (0.7); 3.8691 (2.2); 3.8488 (0.7); 3.8348 (1.5); 3.8140 (0.9); 3.0513 (0.8); 3.0373 (0.8); 3.0060 (1.2); 2.9912 (1.1); 2.8045 (0.4); 2.7814 (1.1); 2.7722 (1.3); 2.7585 (1.4); 2.7378 (1.6); 2.7271 (1.2); 2.7121 (0.7); 2.6932 (1.5); 2.6814 (16.0); 2.3301 (12.1); 1.6054 (4.2); 1.3710 (0.3); 1.3460 (0.6); 1.3047 (2.8); 1.2619 (0.5); 1.1729 (8.7); 1.1643 (9.0); 1.1498 (8.7); 1.1413 (8.6); 0.9419 (1.0); 0.9205 (2.8); 0.8971 (1.1); 0.0492 (0.6); 0.0385 (12.4); 0.0278 (0.7) I-036: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.0518 (2.5); 7.9605 (2.4); 7.6169 (0.4); 7.5937 (0.7); 7.5687 (0.4); 7.5290 (0.3); 7.5025 (0.7); 7.4794 (0.4); 7.3953 (0.6); 7.3675 (0.8); 7.3535 (1.4); 7.3467 (1.5); 7.2989 (10.8); 7.1995 (1.0); 7.1720 (1.4); 7.0196 (0.8); 7.0131 (0.8); 6.9924 (0.6); 6.9857 (0.6); 6.0153 (0.7); 5.3368 (0.4); 4.1899 (0.5); 4.1803 (0.6); 4.1544 (0.7); 4.1445 (0.8); 4.0605 (0.4); 4.0448 (0.4); 4.0333 (0.4); 3.9898 (0.8); 3.746 (0.5); 3.9538 (0.6); 3.9386 (0.4); 3.2016 (0.4); 3.1843 (0.4); 3.1568 (0.7); 3.1393 (0.7); 3.0406 (0.8); 3.0105 (1.1); 2.9931 (16.0); 2.9670 (0.6); 2.9195 (14.7); 2.6942 (7.4); 1.6281 (0.4); 1.2897 (0.4); 0.1046 (1.3); 0.0352 (11.7) I-037: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.5712 (0.6); 7.5456 (2.0); 7.5210 (5.3); 7.4961 (0.7); 7.4253 (2.8); 7.3852 (1.2); 7.3784 (1.8); 7.3714 (1.2); 7.3554 (1.2); 7.2992 (11.9); 7.0362 (3.3); 7.0171 (1.6); 6.9915 (3.9); 6.9666 (2.6); 6.9409 (0.9); 5.7875 (0.8); 5.7693 (0.8); 4.9664 (1.9); 4.1941 (0.9); 4.1703 (3.2); 4.1465 (2.9); 4.1393 (1.5); 4.1234 (1.7); 3.9538 (0.6); 3.9445 (0.8); 3.9346 (0.9); 3.9245 (1.0); 3.9149 (0.9); 3.9051 (0.7); 3.8308 (1.5); 3.8111 (1.1); 3.7941 (1.3); 3.7746 (0.9); 3.3482 (0.3); 3.3304 (0.4); 3.2743 (9.2); 3.2562 (9.2); 3.0161 (0.9); 2.9972 (0.9); 2.9699 (1.4); 2.9511 (1.4); 2.8211 (1.4); 2.7921 (1.4); 2.7751 (1.0); 2.7457 (0.8); 2.3202 (15.4); 2.3054 (16.0); 2.0826 (11.0); 1.6119 (12.6); 1.3209 (3.1); 1.2970 (6.8); 1.2733 (3.1); 0.0378 (13.7) I-038: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.9415 (5.3); 7.5621 (3.4); 7.5520 (4.7); 7.3731 (2.5); 7.2786 (0.9); 7.2700 (1.5); 7.2613 (6.6); 7.0422 (2.4); 7.0265 (2.7); 6.9821 (3.0); 6.9790 (3.3); 6.6343 (1.6); 6.6312 (1.7); 6.6187 (1.6); 6.6156 (1.7); 6.0883 (1.8); 5.2981 (3.5); 4.1991 (1.1); 4.1926 (1.3); 4.1773 (1.4); 4.1708 (1.5); 3.9875 (0.6); 3.9732 (0.9); 3.9694 (0.9); 3.9645 (0.9); 3.9592 (0.7); 3.8646 (1.5); 3.8536 (1.3); 3.8428 (1.4); 3.8317 (1.2); 3.1161 (1.0); 3.1065 (1.1); 3.0890 (1.4); 3.0794 (1.4); 2.8777 (1.3); 2.8589 (1.3); 2.8507 (1.2); 2.8318 (1.0); 2.6456 (16.0); 1.7310 (0.7); 1.7241 (0.8); 1.7143 (1.4); 1.7044 (0.9); 1.6976 (0.8); 1.6875 (0.4); 1.5834 (8.5); 1.2547 (0.4); 0.9329 (2.8); 0.9303 (3.1); 0.9162 (3.0); 0.9136 (3.1); 0.8994 (0.5); 0.8911 (0.4); 0.5625 (0.3); 0.5597 (0.4); 0.5523 (0.4); 0.5433 (1.6); 0.5330 (1.7); 0.5299 (1.8); 0.5255 (1.9); 0.5154 (1.7); 0.5002 (0.5); 0.4967 (0.5); −0.0002 (6.7) I-039: ¹H-NMR(400.1 MHz, CDCl3): δ = 8.1051 (5.7); 7.4339 (1.4); 7.4140 (2.8); 7.3942 (1.6); 7.2586 (39.1); 7.1119 (2.3); 7.0923 (2.0); 7.0155 (3.4); 6.9954 (0.5); 6.9506 (4.4); 6.9312 (4.5); 6.8850 (3.7); 6.6719 (2.0); 6.6530 (1.8); 6.1858 (2.4); 4.2683 (1.4); 4.2612 (1.5); 4.2420 (1.6); 4.2348 (1.6); 3.8524 (1.0); 3.8406 (1.1); 3.8288 (0.9); 3.8057 (2.1); 3.7898 (1.1); 3.7792 (1.8); 3.7635 (1.1); 3.0013 (1.2); 2.9900 (1.2); 2.9673 (1.5); 2.9556 (1.4); 2.7062 (1.4); 2.6820 (1.4); 2.6724 (1.3); 2.6480 (1.1); 2.3027 (0.5); 2.2879 (0.4); 2.2618 (16.0); 2.2313 (0.4); 2.2192 (0.3); 2.1654 (15.0); 2.1436 (0.8); 1.5791 (1.9); 1.5599 (4.7); 1.5324 (10.1); 1.5173 (6.4); 1.4972 (2.5); 1.4326 (0.6); 1.3673 (0.4); 1.3331 (0.5); 1.2558 (4.3); 1.2172 (0.8); 1.2002 (0.7); 1.1534 (0.4); 1.1259 (0.9); 1.1081 (3.1); 1.0889 (3.2); 1.0705 (0.9); 0.8804 (0.7); 0.8600 (2.3); 0.8445 (2.8); −0.0002 (46.5) I-040: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.0064 (5.0); 7.5969 (1.4); 7.5759 (4.0); 7.4850 (1.8); 7.4396 (0.8); 7.4299 (1.3); 7.4227 (0.9); 7.4080 (2.9); 7.4010 (1.3); 7.3865 (1.4); 7.3792 (5.7); 7.3729 (1.1); 7.3446 (5.4); 7.3375 (1.3); 7.3224 (0.9); 7.3161 (2.1); 7.2984 (12.1); 6.2825 (1.2); 5.3368 (1.8); 4.8171 (0.6); 4.8101 (0.6); 4.8042 (0.7); 4.7964 (1.1); 4.7885 (0.7); 4.7826 (0.7); 4.7757 (0.6); 4.3523 (0.9); 4.3393 (0.9); 4.3154 (1.0); 4.3023 (1.0); 4.1933 (0.3); 4.1696 (1.0); 4.1457 (1.1); 4.1223 (0.5); 4.1009 (0.4); 3.8470 (1.4); 3.8250 (1.4); 3.8100 (1.3); 3.7881 (1.2); 2.7339 (16.0); 2.0810 (6.1); 1.6215 (0.4); 1.5974 (1.2); 1.3198 (1.4); 1.2960 (3.0); 1.2722 (1.3); 0.9972 (0.3); 0.9727 (0.7); 0.0483 (0.5); 0.0375 (13.5); 0.0266 (0.5) I-041: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.5778 (0.7); 7.5519 (2.1); 7.5283 (5.4); 7.5050 (0.7); 7.4129 (2.8); 7.3759 (1.4); 7.3686 (2.0); 7.3614 (1.3); 7.3461 (1.4); 7.2989 (14.2); 7.0299 (3.2); 7.0117 (1.8); 6.9861 (3.8); 6.9541 (2.3); 6.9266 (1.0); 6.0253 (1.5); 4.9370 (2.0); 4.1977 (1.1); 4.1858 (1.2); 4.1698 (0.7); 4.1615 (1.3); 4.1495 (1.4); 3.9180 (0.8); 3.9079 (0.9); 3.8991 (1.0); 3.8905 (0.9); 3.8794 (0.8); 3.8601 (0.4); 3.8009 (1.8); 3.7793 (1.3); 3.7645 (1.5); 3.7430 (1.2); 3.2025 (0.5); 3.1918 (0.8); 3.1796 (1.2); 3.1702 (1.2); 3.1577 (0.9); 3.1480 (0.6); 3.1352 (0.3); 2.9992 (0.9); 2.9803 (0.9); 2.9528 (1.4); 2.9336 (1.3); 2.7913 (1.5); 2.7620 (1.4); 2.7451 (1.2); 2.7160 (1.0); 2.3508 (0.7); 2.3151 (14.6); 2.2969 (16.0); 2.2303 (0.6); 2.2023 (0.3); 2.1853 (0.5); 2.1787 (0.4); 2.0824 (2.2); 1.9749 (1.0); 1.6375 (1.4); 1.3205 (0.6); 1.2966 (1.4); 1.2729 (0.6); 0.9955 (0.4); 0.9725 (0.8); 0.9613 (0.8); 0.9486 (1.1); 0.9384 (1.1); 0.9297 (1.2); 0.9253 (1.2); 0.9182 (1.5); 0.9055 (1.6); 0.8942 (1.2); 0.8868 (1.3); 0.8781 (1.3); 0.8646 (1.2); 0.8532 (0.9); 0.8464 (0.8); 0.8313 (0.7); 0.8123 (0.6); 0.7938 (0.5); 0.7648 (0.6); 0.7503 (0.8); 0.7300 (1.0); 0.7162 (1.4); 0.6991 (1.5); 0.6865 (0.9); 0.6681 (0.8); 0.6560 (1.4); 0.6439 (1.1); 0.6371 (1.4); 0.6236 (1.1); 0.6107 (0.7); 0.6034 (0.7); 0.5900 (0.5); 0.5697 (0.4); 0.5530 (0.4); 0.5352 (0.5); 0.5165 (0.4); 0.5002 (0.3); 0.1077 (8.2); 0.0481 (0.6); 0.0373 (17.4); 0.0266 (1.5) I-042: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.7320 (5.6); 7.6696 (3.1); 7.6666 (2.8); 7.6577 (1.4); 7.6524 (2.1); 7.3995 (1.6); 7.3541 (0.7); 7.3452 (0.7); 7.3354 (1.0); 7.3291 (0.8); 7.3240 (0.6); 7.3157 (0.5); 7.2989 (8.7); 7.0075 (1.6); 6.9819 (1.9); 6.9263 (1.9); 6.7168 (1.0); 6.6912 (0.8); 5.9713 (1.2); 4.3525 (0.7); 4.3430 (0.8); 4.3174 (0.9); 4.3084 (0.9); 3.9512 (0.3); 3.9366 (0.5); 3.9297 (0.4); 3.9183 (0.5); 3.9084 (0.4); 3.9021 (0.5); 3.8876 (1.8); 3.8669 (0.6); 3.8529 (1.3); 3.8320 (0.8); 3.0708 (0.6); 3.0567 (0.6); 3.0258 (0.9); 3.0106 (0.8); 2.8013 (16.0); 2.7738 (1.0); 2.7414 (0.9); 2.7286 (0.8); 2.6955 (0.7); 2.3075 (10.5); 2.1886 (9.7); 1.6012 (15.3); 1.3601 (0.3); 1.3432 (0.6); 1.3038 (3.7); 0.9409 (1.3); 0.9192 (4.2); 0.8959 (1.6); 0.1075 (1.1); 0.0372 (9.7); 0.0264 (0.4) I-043: ¹H-NMR(499.9 MHz, d₆-DMSO): δ = 7.8070 (0.5); 7.5225 (1.4); 7.5062 (3.2); 7.4899 (2.0); 7.4263 (1.8); 7.4210 (1.7); 7.3783 (1.5); 7.3769 (1.6); 7.3746 (1.7); 7.3732 (1.5); 7.3622 (1.2); 7.3607 (1.2); 7.3585 (1.4); 7.3572 (1.2); 7.3255 (2.1); 7.3213 (3.3); 7.3171 (1.7); 7.2362 (1.5); 7.2348 (1.6); 7.2318 (1.4); 7.2198 (1.4); 7.2184 (1.3); 7.2154 (1.3); 7.0407 (2.1); 7.0254 (2.4); 6.9556 (2.7); 6.8623 (1.5); 6.8472 (1.3); 4.0573 (0.4); 4.0430 (1.1); 4.0288 (1.1); 4.0146 (0.4); 3.7869 (1.0); 3.7700 (2.6); 3.7635 (2.8); 3.7603 (2.8); 3.7351 (0.8); 3.3236 (16.8); 2.8005 (1.5); 2.7877 (2.2); 2.7778 (1.2); 2.7621 (0.3); 2.6728 (16.0); 2.5136 (1.3); 2.5103 (2.3); 2.5068 (2.9); 2.5032 (2.1); 2.4608 (0.6); 2.3486 (0.5); 2.2639 (0.5); 2.2354 (12.6); 2.2198 (11.8); 2.1545 (0.3); 1.9945 (4.7); 1.1954 (1.3); 1.1812 (2.5); 1.1670 (1.2) I-044: ¹H-NMR(600.1 MHz, d₆-DMSO): δ = 8.0423 (0.4); 8.0383 (0.5); 5.7559 (0.9); 3.3179 (16.0); 2.5188 (0.4); 2.5157 (0.4); 2.5069 (7.0); 2.5039 (15.0); 2.5008 (20.9); 2.4978 (15.5); 2.4948 (7.4); 2.2309 (0.8); 2.2267 (0.8); 2.1867 (0.7); 2.1834 (0.7); −0.0001 (1.0) I-045: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9417 (5.1); 7.2986 (13.9); 7.1243 (0.6); 7.1204 (0.6); 7.0977 (1.4); 7.0940 (1.4); 7.0713 (1.0); 7.0676 (1.1); 7.0088 (0.9); 7.0031 (1.1); 6.9812 (3.3); 6.9529 (1.2); 6.9282 (1.8); 6.9232 (1.8); 6.9069 (2.7); 6.8815 (0.8); 6.8479 (0.7); 6.8424 (0.7); 6.8212 (1.2); 6.7996 (0.6); 6.7946 (0.6); 6.2640 (1.3); 5.3372 (10.4); 4.2937 (0.8); 4.2838 (0.9); 4.2583 (1.0); 4.2478 (1.0); 3.9239 (0.4); 3.9075 (0.6); 3.8959 (0.5); 3.8756 (0.4); 3.8698 (0.3); 3.8274 (1.7); 3.8058 (1.0); 3.7917 (1.3); 3.7703 (0.9); 2.9967 (0.7); 2.9797 (0.7); 2.9517 (1.0); 2.9352 (0.9); 2.7207 (1.2); 2.6896 (1.1); 2.6757 (1.1); 2.6617 (16.0); 2.6449 (0.9); 2.1415 (11.0); 2.1161 (11.1); 2.0928 (0.7); 2.0830 (1.4); 1.5960 (12.1); 1.3213 (0.4); 1.3057 (0.4); 1.2975 (0.8); 1.0859 (0.6); 1.0722 (1.6); 1.0653 (1.8); 1.0519 (1.0); 1.0435 (1.7); 1.0369 (1.7); 1.0237 (0.8); 0.8264 (0.9); 0.8127 (1.7); 0.8092 (2.0); 0.8047 (1.6); 0.7955 (1.9); 0.7927 (1.8); 0.7877 (1.4); 0.7755 (0.6); 0.1080 (6.3); 0.0491 (0.6); 0.0384 (16.0); 0.0274 (0.6) I-046: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.7600 (4.2); 8.7483 (4.1); 8.7364 (0.5); 8.7241 (0.3); 8.5985 (7.4); 8.5708 (0.4); 7.9420 (5.2); 7.9326 (3.7); 7.9298 (4.8); 7.6179 (5.3); 7.6171 (5.3); 7.6087 (3.1); 7.6067 (3.1); 7.5902 (0.4); 7.3692 (3.0); 7.3125 (1.2); 7.3077 (1.5); 7.3010 (1.6); 7.2970 (1.4); 7.2900 (0.9); 7.2612 (8.2); 6.9781 (2.7); 6.9629 (2.9); 6.8904 (3.4); 6.6719 (1.9); 6.6570 (1.7); 6.2023 (2.5); 4.3392 (1.4); 4.3328 (1.5); 4.3177 (1.6); 4.3113 (1.5); 4.1279 (0.9); 4.1136 (0.9); 3.9296 (0.7); 3.9216 (1.0); 3.9100 (1.0); 3.9026 (0.8); 3.8585 (2.0); 3.8456 (1.4); 3.8369 (1.8); 3.8241 (1.3); 3.0390 (1.2); 3.0300 (1.2); 3.0117 (1.4); 3.0026 (1.3); 2.7316 (1.4); 2.7113 (1.5); 2.7043 (1.3); 2.6840 (1.2); 2.3245 (1.0); 2.3041 (1.1); 2.2803 (16.0); 2.1499 (15.2); 2.0432 (4.2); 1.6182 (7.0); 1.2726 (1.0); 1.2583 (2.1); 1.2440 (1.0); −0.0002 (9.6) I-047: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.3164 (0.4); 8.0962 (9.8); 7.9525 (1.7); 7.4134 (2.1); 7.4052 (2.1); 7.3427 (0.5); 7.3280 (1.7); 7.3218 (3.4); 7.3189 (3.8); 7.3082 (2.1); 7.3038 (4.3); 7.2837 (1.0); 7.2330 (1.2); 7.2274 (1.3); 7.2146 (1.8); 7.2087 (1.0); 7.2049 (1.1); 7.2009 (0.9); 7.1906 (0.7); 7.0533 (2.7); 7.0342 (3.2); 6.9293 (3.3); 6.8264 (1.8); 6.8072 (1.5); 3.7543 (5.3); 3.7401 (1.0); 3.7307 (1.4); 3.7213 (1.1); 3.7127 (0.8); 3.7038 (0.5); 3.3314 (34.7); 2.8908 (11.4); 2.8461 (0.3); 2.8282 (0.4); 2.8112 (1.8); 2.8005 (2.3); 2.7955 (2.2); 2.7838 (1.9); 2.7664 (0.4); 2.7320 (10.0); 2.5455 (24.0); 2.5250 (0.7); 2.5201 (1.0); 2.5114 (12.8); 2.5071 (26.0); 2.5026 (34.4); 2.4981 (25.7); 2.4938 (13.0); 2.2401 (16.0); 2.1912 (14.7); −0.0002 (6.2) I-048: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1592 (8.0); 7.3738 (0.5); 7.3466 (1.2); 7.3250 (1.1); 7.2987 (11.0); 7.2745 (2.0); 7.2690 (2.1); 7.2466 (0.9); 7.2412 (1.1); 7.2000 (1.3); 7.1941 (1.3); 7.1785 (1.3); 7.1724 (1.9); 7.1669 (0.8); 7.1516 (0.8); 7.1454 (0.8); 7.0113 (2.5); 6.9858 (2.9); 6.9083 (2.9); 6.7238 (1.6); 6.6993 (1.4); 6.0356 (1.9); 4.3301 (1.1); 4.3210 (1.4); 4.2955 (1.5); 4.2864 (1.4); 3.9198 (0.8); 3.9096 (0.7); 3.9039 (0.8); 3.8972 (0.6); 3.8881 (0.7); 3.8756 (2.8); 3.8554 (0.8); 3.8411 (1.9); 3.8205 (1.2); 3.0596 (1.0); 3.0446 (1.0); 3.0146 (1.4); 2.9986 (1.3); 2.7801 (1.4); 2.7486 (1.3); 2.7350 (1.2); 2.7029 (1.1); 2.3073 (16.0); 2.1635 (15.1); 1.6012 (0.8); 1.3716 (0.4); 1.2931 (7.9); 1.0386 (0.4); 1.0162 (0.4); 0.9186 (0.7); 0.8946 (0.8); 0.8806 (0.7); 0.0492 (0.3); 0.0382 (11.7); 0.0275 (0.5) I-049: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.3142 (1.5); 8.2404 (15.3); 8.0564 (3.1); 8.0466 (3.1); 7.7721 (4.3); 7.7680 (3.5); 7.7464 (2.7); 7.7267 (3.6); 7.6950 (5.1); 7.6896 (3.0); 7.6742 (8.2); 7.6689 (8.0); 7.5448 (4.7); 7.5238 (6.3); 7.4038 (3.6); 7.3985 (3.4); 7.3828 (2.7); 7.3774 (2.6); 5.7544 (16.0); 5.1088 (1.0); 5.1010 (2.8); 5.0919 (2.8); 5.0833 (1.0); 4.0629 (1.7); 4.0544 (1.9); 4.0349 (2.8); 4.0265 (2.4); 3.9250 (2.3); 3.9167 (2.3); 3.8969 (1.7); 3.8888 (1.6); 3.3172 (234.5); 2.6932 (0.7); 2.6791 (1.7); 2.6747 (3.6); 2.6702 (5.0); 2.6656 (3.7); 2.6610 (1.7); 2.5237 (14.7); 2.5189 (21.5); 2.5102 (297.3); 2.5058 (611.1); 2.5012 (807.2); 2.4966 (578.2); 2.4921 (277.7); 2.3372 (1.6); 2.3326 (3.6); 2.3280 (5.0); 2.3235 (3.7); 2.3189 (1.7); 2.0734 (1.7); 1.9882 (1.2); 1.2346 (1.0); 1.1927 (0.5); 1.1749 (0.8); 1.1570 (0.4); 0.1548 (0.5); 0.1458 (1.2); 0.1224 (3.6); 0.0879 (3.0); 0.0814 (0.5); 0.0656 (0.3); 0.0573 (2.4); 0.0080 (8.2); −0.0002 (284.6); −0.0085 (9.3); −0.1497 (1.1) I-050: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9516 (5.1); 7.3391 (1.3); 7.3128 (2.8); 7.2984 (13.2); 7.2866 (1.9); 7.0024 (2.6); 6.9768 (2.9); 6.9335 (2.4); 6.8479 (1.2); 6.8450 (1.2); 6.8402 (1.4); 6.8213 (1.0); 6.8182 (1.0); 6.8134 (1.4); 6.7890 (1.9); 6.7831 (2.4); 6.7198 (1.4); 6.6947 (1.1); 6.3121 (1.5); 5.3370 (7.4); 4.2646 (0.8); 4.2561 (1.2); 4.2307 (1.2); 4.2216 (1.0); 4.1953 (0.4); 4.1715 (1.1); 4.1477 (1.1); 4.1241 (0.5); 3.8750 (0.7); 3.8651 (0.7); 3.8596 (0.7); 3.8526 (0.7); 3.8374 (2.3); 3.8176 (0.6); 3.8035 (1.5); 3.7827 (0.9); 3.0246 (0.7); 3.0101 (0.8); 2.9803 (1.1); 2.9642 (1.1); 2.7638 (1.1); 2.7330 (1.1); 2.7181 (1.1); 2.6871 (1.0); 2.6649 (16.0); 2.2984 (12.2); 2.2308 (11.6); 2.0831 (5.5); 2.0442 (1.5); 1.9841 (0.4); 1.9673 (0.6); 1.9558 (0.7); 1.9394 (1.2); 1.9226 (0.8); 1.9116 (0.7); 1.8944 (0.4); 1.6054 (14.1); 1.3210 (1.5); 1.2971 (2.9); 1.2733 (1.4); 1.0531 (0.8); 1.0383 (2.1); 1.0313 (2.3); 1.0165 (1.3); 1.0098 (2.2); 1.0033 (2.1); 0.9886 (1.1); 0.9733 (0.5); 0.7682 (1.0); 0.7532 (2.6); 0.7481 (2.3); 0.7366 (2.3); 0.7313 (2.6); 0.7148 (0.9); 0.1073 (0.9); 0.0483 (0.6); 0.0376 (13.3); 0.0268 (0.9) I-051: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.1253 (7.9); 7.6006 (0.5); 7.5856 (5.1); 7.5709 (2.1); 7.5552 (0.6); 7.3128 (2.5); 7.2593 (9.1); 7.2432 (1.0); 7.2391 (1.4); 7.2292 (1.0); 7.2250 (1.6); 7.2206 (0.7); 6.9450 (2.5); 6.9298 (2.8); 6.8791 (2.9); 6.6589 (1.5); 6.6438 (1.4); 6.0731 (1.8); 5.2975 (6.2); 4.2956 (1.3); 4.2890 (1.4); 4.2740 (1.4); 4.2674 (1.4); 3.8848 (0.5); 3.8809 (0.5); 3.8770 (0.7); 3.8715 (0.6); 3.8682 (0.6); 3.8647 (0.8); 3.8609 (0.6); 3.8574 (0.6); 3.8550 (0.5); 3.8136 (2.1); 3.8008 (1.4); 3.7919 (1.8); 3.7792 (1.4); 3.0080 (1.1); 2.9988 (1.1); 2.9806 (1.3); 2.9714 (1.2); 2.6946 (1.4); 2.6744 (1.4); 2.6672 (1.3); 2.6469 (1.2); 2.2591 (16.0); 2.1419 (14.8); 1.5511 (4.3); −0.0002 (8.6) I-052: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.9145 (5.3); 7.2597 (11.3); 7.0779 (0.7); 7.0620 (1.6); 7.0461 (1.0); 6.9827 (1.9); 6.9752 (0.9); 6.9720 (1.1); 6.9674 (2.3); 6.9581 (1.4); 6.9448 (0.6); 6.9418 (0.6); 6.8703 (2.2); 6.8100 (0.7); 6.8073 (0.7); 6.7943 (1.3); 6.7811 (0.6); 6.7785 (0.6); 6.6683 (1.2); 6.6534 (1.1); 6.2105 (1.4); 5.2980 (0.9); 4.2377 (0.9); 4.2312 (1.0); 4.2163 (1.1); 4.2098 (1.1); 3.8698 (0.4); 3.8628 (0.5); 3.8590 (0.6); 3.8553 (0.5); 3.8518 (0.6); 3.8483 (0.6); 3.8401 (0.5); 3.8358 (0.3); 3.8132 (1.6); 3.8009 (0.9); 3.7918 (1.4); 3.7795 (1.0); 2.9882 (0.8); 2.9781 (0.8); 2.9610 (1.0); 2.9507 (1.0); 2.7468 (1.1); 2.7279 (1.1); 2.7197 (0.9); 2.7007 (0.8); 2.6274 (16.0); 2.2715 (11.9); 2.1441 (11.3); 2.0931 (0.5); 2.0865 (0.6); 2.0762 (1.0); 2.0660 (0.6); 2.0593 (0.6); 2.0044 (0.4); 1.5590 (15.4); 1.0340 (0.6); 1.0313 (0.8); 1.0272 (1.3); 1.0243 (1.7); 1.0182 (1.4); 1.0146 (1.0); 1.0106 (1.4); 1.0073 (1.7); 1.0031 (0.9); 0.7832 (1.1); 0.7794 (0.9); 0.7753 (1.6); 0.7721 (1.7); 0.7685 (1.8); 0.7658 (1.7); 0.7610 (0.9); 0.7579 (1.1); 0.0063 (0.4); −0.0002 (13.0); −0.0066 (0.7) I-053: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.1251 (7.5); 7.6004 (0.7); 7.5977 (0.7); 7.5855 (5.2); 7.5708 (2.1); 7.5552 (0.6); 7.3128 (2.6); 7.2592 (8.6); 7.2432 (1.2); 7.2391 (1.5); 7.2291 (1.1); 7.2250 (1.6); 7.2206 (0.8); 6.9450 (2.6); 6.9297 (2.8); 6.8793 (3.0); 6.6591 (1.7); 6.6441 (1.4); 6.0734 (1.9); 5.2974 (6.3); 4.2954 (1.4); 4.2887 (1.4); 4.2738 (1.5); 4.2671 (1.4); 3.8846 (0.6); 3.8808 (0.7); 3.8768 (0.8); 3.8680 (0.7); 3.8647 (0.9); 3.8609 (0.6); 3.8573 (0.6); 3.8448 (0.3); 3.8135 (2.1); 3.8007 (1.4); 3.7918 (1.8); 3.7791 (1.4); 3.0079 (1.2); 2.9987 (1.2); 2.9805 (1.4); 2.9713 (1.3); 2.6946 (1.5); 2.6744 (1.5); 2.6672 (1.3); 2.6469 (1.2); 2.3031 (0.4); 2.2590 (16.0); 2.1419 (14.9); 1.5522 (3.8); 0.0059 (0.5); −0.0002 (7.9); −0.0066 (0.3) I-054: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.0002 (5.3); 7.6152 (0.4); 7.5885 (1.5); 7.5663 (4.4); 7.5442 (0.4); 7.4950 (2.2); 7.4560 (0.9); 7.4480 (1.4); 7.4405 (0.9); 7.4256 (0.9); 7.2991 (7.1); 7.2649 (3.1); 7.2424 (2.2); 7.1598 (1.7); 7.1334 (1.1); 6.2020 (1.7); 5.3382 (0.9); 4.7865 (0.7); 4.7718 (0.9); 4.7627 (0.9); 4.7479 (0.8); 4.3983 (1.0); 4.3845 (1.0); 4.3614 (1.1); 4.3477 (1.0); 3.7639 (1.4); 3.7383 (1.4); 3.7272 (1.3); 3.7015 (1.2); 2.9523 (1.9); 2.9277 (3.7); 2.9025 (2.7); 2.8750 (1.6); 2.8450 (1.6); 2.8187 (0.8); 2.7904 (0.4); 2.7326 (16.0); 2.1522 (0.7); 2.1274 (2.3); 2.1026 (3.2); 2.0779 (2.0); 2.0530 (0.5); 1.6084 (2.7); 1.2937 (0.4); 0.0489 (0.4); 0.0383 (9.1) I-055: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.5891 (0.4); 7.5632 (1.3); 7.5376 (3.5); 7.5133 (0.4); 7.4448 (1.9); 7.4118 (0.8); 7.4048 (1.3); 7.3976 (0.7); 7.3871 (0.5); 7.3813 (0.8); 7.3745 (0.5); 7.2990 (7.3); 7.0373 (1.7); 7.0261 (2.1); 7.0126 (2.5); 6.9469 (1.3); 6.9205 (0.8); 4.7215 (1.3); 4.1991 (1.0); 4.1734 (1.2); 3.9658 (0.3); 3.9562 (0.5); 3.9327 (1.7); 3.9277 (1.4); 3.9192 (0.7); 3.9099 (0.6); 3.9018 (1.3); 3.8847 (0.6); 3.0322 (0.5); 3.0162 (0.5); 2.9866 (1.0); 2.9699 (0.9); 2.9049 (0.9); 2.8753 (0.8); 2.8593 (0.5); 2.8291 (0.4); 2.6255 (14.3); 2.4371 (14.2); 2.3169 (16.0); 1.6242 (3.6); 0.0376 (7.7) I-056: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.9093 (3.3); 7.2606 (12.8); 7.2105 (3.5); 7.1071 (1.0); 7.0912 (2.3); 7.0754 (1.5); 7.0278 (0.3); 7.0200 (0.4); 7.0044 (0.9); 6.9857 (4.1); 6.9770 (5.6); 6.9604 (1.8); 6.8265 (1.1); 6.8130 (1.9); 6.7994 (1.0); 6.1910 (2.0); 4.1948 (0.5); 4.1842 (1.6); 4.1690 (1.7); 4.1582 (0.6); 3.8500 (2.8); 3.8347 (2.7); 3.8240 (1.0); 2.9674 (1.1); 2.9582 (1.1); 2.9401 (1.4); 2.9306 (1.4); 2.8002 (1.2); 2.7825 (1.2); 2.7734 (1.0); 2.7626 (0.4); 2.7547 (0.9); 2.7252 (0.6); 2.6347 (14.4); 2.3286 (0.8); 2.3216 (0.4); 2.3131 (0.5); 2.2860 (16.0); 2.1092 (0.4); 2.0988 (0.8); 2.0921 (0.9); 2.0819 (1.5); 2.0718 (1.0); 2.0651 (0.9); 2.0546 (0.5); 1.5859 (0.4); 1.2548 (0.8); 1.0426 (0.5); 1.0329 (2.5); 1.0295 (2.7); 1.0161 (2.7); 1.0126 (2.7); 1.0033 (0.8); 0.9930 (0.5); 0.9826 (0.4); 0.8088 (0.3); 0.7919 (1.7); 0.7817 (2.6); 0.7788 (2.8); 0.7768 (2.9); 0.7666 (1.9); 0.7535 (0.5); 0.7480 (0.6); 0.7386 (0.4); −0.0002 (15.6) I-057: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9592 (5.2); 7.2995 (12.8); 7.1388 (0.7); 7.1124 (1.8); 7.0860 (1.4); 7.0315 (2.9); 7.0051 (3.6); 6.9819 (0.6); 6.9767 (0.6); 6.8597 (1.0); 6.8412 (3.7); 6.8170 (0.8); 6.8129 (0.7); 6.5738 (1.4); 6.5481 (1.2); 6.2798 (1.7); 5.3386 (8.0); 4.2659 (1.2); 4.2411 (1.4); 3.8811 (0.7); 3.8576 (2.0); 3.8245 (1.6); 3.8041 (0.8); 3.0342 (0.7); 3.0188 (0.8); 2.9889 (1.2); 2.9733 (1.2); 2.7860 (1.0); 2.7655 (0.7); 2.7553 (1.0); 2.7406 (0.9); 2.7099 (0.7); 2.6679 (16.0); 2.3524 (0.8); 2.3123 (12.8); 2.1571 (0.5); 2.1456 (0.6); 2.1286 (1.1); 2.1117 (0.7); 2.1011 (0.7); 2.0842 (0.5); 1.7700 (0.6); 1.7585 (0.6); 1.7419 (1.2); 1.7254 (0.7); 1.7138 (0.6); 1.6965 (0.3); 1.6000 (12.3); 1.2947 (0.4); 1.0883 (0.7); 1.0738 (1.5); 1.0686 (2.0); 1.0610 (1.5); 1.0558 (1.4); 1.0460 (1.7); 1.0402 (2.0); 1.0271 (1.0); 0.9081 (2.7); 0.8848 (2.5); 0.8803 (2.5); 0.8571 (0.4); 0.8361 (1.0); 0.8206 (2.2); 0.8137 (2.2); 0.8045 (2.4); 0.7878 (0.9); 0.5893 (0.4); 0.5735 (1.3); 0.5523 (1.6); 0.5442 (1.5); 0.5273 (1.3); 0.5148 (0.3); 0.1080 (1.2); 0.0385 (16.6) I-058: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.2993 (16.7); 7.1281 (2.1); 7.1179 (1.4); 7.1148 (1.5); 7.1030 (2.7); 7.0558 (1.4); 7.0301 (2.1); 7.0149 (2.0); 6.9399 (1.1); 6.9148 (0.7); 6.8558 (0.5); 6.8453 (0.5); 6.8343 (1.0); 6.8227 (0.8); 6.8134 (0.4); 6.8018 (0.4); 4.7922 (1.2); 4.2187 (0.9); 4.1935 (1.0); 3.9560 (0.5); 3.9469 (0.5); 3.9281 (1.6); 3.9104 (0.6); 3.8946 (1.1); 3.8764 (0.6); 3.0399 (0.4); 3.0230 (0.4); 2.9935 (0.9); 2.9765 (0.8); 2.8977 (0.7); 2.8683 (0.7); 2.8514 (0.5); 2.8227 (0.4); 2.5587 (12.9); 2.3218 (9.9); 2.3084 (9.4); 2.1237 (0.4); 2.1119 (0.5); 2.0950 (0.8); 2.0784 (0.5); 2.0667 (0.5); 1.5883 (16.0); 1.2927 (0.5); 1.0784 (0.4); 1.0635 (1.3); 1.0573 (1.6); 1.0427 (0.7); 1.0351 (1.5); 1.0288 (1.6); 1.0144 (0.6); 0.8218 (0.6); 0.8077 (1.7); 0.8019 (1.8); 0.7907 (1.6); 0.7846 (1.8); 0.7694 (0.6); 0.1079 (4.9); 0.0494 (0.6); 0.0385 (21.6); 0.0279 (1.1) I-059: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.1139 (8.8); 7.5958 (0.6); 7.5933 (0.6); 7.5813 (5.2); 7.5667 (2.1); 7.5510 (0.6); 7.3129 (2.5); 7.2580 (3.0); 7.2422 (1.0); 7.2381 (1.4); 7.2282 (1.1); 7.2240 (1.6); 7.2196 (0.7); 6.9438 (2.6); 6.9285 (2.8); 6.8774 (2.9); 6.6591 (1.6); 6.6441 (1.4); 6.0812 (1.8); 4.2843 (1.3); 4.2779 (1.3); 4.2627 (1.4); 4.2562 (1.4); 3.8805 (0.6); 3.8767 (0.6); 3.8730 (0.8); 3.8672 (0.7); 3.8641 (0.7); 3.8605 (0.8); 3.8567 (0.6); 3.8534 (0.6); 3.8510 (0.6); 3.8091 (2.2); 3.7964 (1.4); 3.7875 (1.9); 3.7748 (1.4); 3.0035 (1.1); 2.9942 (1.1); 2.9760 (1.3); 2.9668 (1.3); 2.6950 (1.4); 2.6748 (1.5); 2.6676 (1.3); 2.6474 (1.2); 2.2563 (16.0); 2.1411 (14.7); 1.5971 (3.6); 1.1369 (0.7); 1.1247 (0.7); −0.0002 (2.5) I-060: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.7742 (4.7); 8.6566 (3.0); 8.6400 (3.1); 8.6154 (6.9); 7.6617 (5.0); 7.6488 (5.2); 7.6447 (4.6); 7.6170 (0.5); 7.4264 (2.4); 7.3760 (1.0); 7.3675 (1.2); 7.3589 (1.5); 7.3523 (1.4); 7.3462 (1.0); 7.3383 (0.8); 7.2986 (12.9); 7.0239 (2.2); 6.9984 (2.6); 6.9324 (2.7); 6.7212 (1.5); 6.6967 (1.3); 6.1765 (1.9); 4.3741 (1.1); 4.3646 (1.2); 4.3388 (1.3); 4.3290 (1.2); 3.9732 (0.6); 3.9590 (0.8); 3.9408 (0.8); 3.9239 (0.7); 3.8933 (2.0); 3.8720 (1.0); 3.8580 (1.6); 3.8366 (1.1); 3.0877 (0.9); 3.0728 (0.9); 3.0417 (1.2); 3.0274 (1.1); 2.7800 (1.2); 2.7470 (1.2); 2.7349 (1.1); 2.7014 (0.9); 2.3610 (0.7); 2.3430 (0.8); 2.3183 (13.3); 2.2498 (0.4); 2.1945 (12.5); 1.6136 (16.0); 1.2928 (0.6); 0.1072 (1.3); 0.0370 (14.8); 0.0263 (1.1) I-061: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.8861 (4.6); 7.4878 (0.5); 7.4724 (1.5); 7.4572 (2.9); 7.4393 (0.4); 7.3795 (1.8); 7.3362 (0.9); 7.3323 (1.3); 7.3283 (0.8); 7.3177 (0.9); 7.2118 (3.5); 7.2079 (1.5); 7.1943 (4.5); 7.1895 (10.0); 6.8319 (3.9); 6.8279 (1.4); 6.8183 (1.5); 6.8145 (3.3); 6.8086 (0.4); 6.0588 (1.4); 5.2277 (3.8); 4.6454 (0.7); 4.6432 (0.7); 4.6374 (0.8); 4.6348 (0.8); 4.6308 (0.8); 4.6225 (0.7); 4.2570 (0.9); 4.2488 (0.9); 4.2348 (1.0); 4.2266 (0.9); 3.7263 (16.0); 3.6518 (1.3); 3.6366 (1.3); 3.6296 (1.2); 3.6145 (1.2); 2.6223 (14.3); 1.9722 (0.5); 1.4836 (4.0); 1.1873 (0.5); −0.0002 (15.1); −0.0645 (1.0); −0.0706 (10.6); −0.0771 (0.4) I-062: ¹H-NMR(499.9 MHz, CDCl3): δ = 9.3730 (0.4); 8.2205 (0.6); 8.0631 (0.4); 7.6952 (0.4); 7.6815 (0.5); 7.6686 (0.4); 7.6548 (0.4); 7.6357 (0.4); 7.6204 (0.4); 7.6019 (0.4); 7.5868 (0.4); 7.5711 (0.4); 7.5568 (0.7); 7.5430 (0.8); 7.5219 (0.6); 7.5101 (0.5); 7.4949 (0.5); 7.4807 (0.5); 7.4668 (0.6); 7.4483 (0.4); 7.4412 (0.4); 7.4335 (0.4); 7.4255 (0.4); 7.3922 (0.5); 7.3780 (0.7); 7.3596 (0.8); 7.3416 (1.0); 7.3267 (0.9); 7.2940 (2.0); 7.2796 (2.5); 7.2601 (19.7); 7.2362 (1.8); 7.2204 (2.3); 7.2051 (1.5); 7.1856 (0.8); 7.1807 (0.8); 7.1701 (1.0); 7.1537 (3.6); 7.1421 (1.6); 7.1255 (1.2); 7.1020 (0.7); 7.0824 (0.4); 7.0446 (2.2); 7.0346 (3.4); 7.0284 (4.8); 6.7240 (0.8); 6.6794 (1.6); 6.6628 (1.4); 6.2983 (2.5); 6.2925 (2.6); 5.6003 (0.6); 5.5858 (1.1); 5.5712 (0.6); 4.6604 (0.3); 4.6449 (0.8); 4.6303 (0.8); 4.6153 (0.4); 4.5481 (1.0); 4.5408 (1.0); 3.7037 (0.4); 3.6803 (16.0); 3.3172 (0.7); 3.2609 (0.6); 3.2161 (0.5); 3.0668 (1.0); 3.0547 (1.0); 3.0441 (1.3); 2.9324 (1.0); 2.8568 (0.8); 2.5180 (1.1); 2.4929 (1.1); 2.4795 (0.9); 2.4619 (0.4); 2.4000 (4.1); 1.9994 (14.5); 1.2982 (0.4); 1.2839 (0.7); 1.2563 (3.5); 0.8936 (0.4); 0.8801 (0.8); 0.8664 (0.5); 0.0062 (0.8); −0.0002 (21.7); −0.0066 (1.2) I-063: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.6578 (5.4); 7.5859 (3.4); 7.5845 (3.1); 7.5789 (1.7); 7.5758 (2.2); 7.3339 (1.8); 7.2798 (0.7); 7.2746 (0.9); 7.2718 (0.6); 7.2683 (1.1); 7.2642 (1.0); 7.2601 (2.9); 6.9650 (1.8); 6.9497 (2.0); 6.8854 (2.1); 6.6821 (1.1); 6.6672 (1.0); 6.0109 (1.4); 5.2949 (4.2); 4.2979 (0.9); 4.2913 (1.0); 4.2763 (1.0); 4.2697 (1.0); 3.9235 (16.0); 3.9051 (0.6); 3.9009 (0.6); 3.8971 (0.7); 3.8914 (0.6); 3.8848 (0.7); 3.8811 (0.5); 3.8776 (0.5); 3.8353 (1.4); 3.8226 (1.0); 3.8137 (1.2); 3.8010 (0.9); 3.0129 (0.7); 3.0037 (0.8); 2.9855 (0.9); 2.9763 (0.9); 2.7226 (1.0); 2.7025 (1.0); 2.6953 (0.9); 2.6751 (0.8); 2.3336 (15.4); 2.2675 (10.8); 2.1527 (10.1); 1.5897 (0.5); −0.0002 (2.8) I-064: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.6875 (5.6); 7.5797 (3.1); 7.5721 (1.5); 7.5693 (2.4); 7.3360 (1.5); 7.2841 (0.7); 7.2792 (0.7); 7.2736 (1.0); 7.2697 (0.9); 7.2660 (0.7); 7.2596 (3.9); 6.9694 (1.6); 6.9542 (1.8); 6.8870 (1.8); 6.6856 (1.0); 6.6706 (0.8); 5.9863 (1.2); 4.2861 (0.8); 4.2800 (0.8); 4.2647 (0.9); 4.2585 (0.9); 4.0366 (16.0); 3.8992 (0.4); 3.8953 (0.4); 3.8902 (0.6); 3.8857 (0.5); 3.8827 (0.4); 3.8793 (0.5); 3.8755 (0.4); 3.8725 (0.4); 3.8695 (0.4); 3.8424 (1.4); 3.8299 (0.8); 3.8209 (1.2); 3.8085 (0.8); 3.0061 (0.7); 2.9969 (0.7); 2.9788 (0.8); 2.9694 (0.8); 2.7318 (0.9); 2.7119 (0.9); 2.7044 (0.8); 2.6845 (0.7); 2.3291 (15.0); 2.2680 (9.8); 2.1537 (9.0); 2.0419 (0.5); 2.0017 (0.9); 1.5664 (1.0); −0.0002 (4.4) I-065: ¹H-NMR(400.1 MHz, d₆-DMSO): δ = 7.7607 (0.8); 7.7412 (2.5); 7.7216 (2.5); 7.7035 (3.2); 7.6840 (1.4); 7.6253 (3.6); 7.6014 (2.2); 7.5814 (1.6); 7.4082 (2.4); 7.4028 (2.5); 7.0822 (2.0); 7.0632 (2.3); 6.9530 (3.7); 6.8487 (1.5); 6.8304 (1.4); 3.8004 (7.4); 3.3444 (21.3); 2.8242 (3.1); 2.8095 (3.0); 2.5137 (4.1); 2.5098 (5.3); 2.5058 (4.0); 2.2356 (14.4); 2.2138 (16.0); 2.0841 (1.5) I-066: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1875 (7.1); 7.6297 (4.7); 7.6125 (3.7); 7.3652 (2.6); 7.3143 (1.0); 7.2983 (13.3); 7.2769 (0.7); 7.0047 (2.5); 6.9792 (3.0); 6.9213 (3.0); 6.7137 (1.6); 6.6886 (1.4); 6.1361 (1.6); 5.3368 (9.5); 5.1204 (0.8); 5.1003 (1.0); 5.0823 (0.9); 4.3441 (1.1); 4.3341 (1.3); 4.3089 (1.4); 4.2989 (1.4); 3.9464 (0.5); 3.9291 (0.7); 3.9127 (0.8); 3.8965 (0.6); 3.8890 (0.6); 3.8737 (2.3); 3.8526 (1.0); 3.8387 (1.8); 3.8177 (1.1); 3.4839 (1.0); 3.4751 (1.3); 3.4595 (1.1); 3.0622 (1.0); 3.0476 (1.0); 3.0169 (1.4); 3.0016 (1.3); 2.7648 (1.2); 2.7322 (1.2); 2.7198 (1.0); 2.6866 (0.9); 2.3035 (16.0); 2.1871 (14.3); 2.0823 (0.8); 1.6094 (10.8); 1.6044 (8.6); 1.5866 (6.3); 1.5822 (6.9); 1.3028 (0.4); 1.2964 (0.7); 1.2797 (0.6); 0.0478 (0.4); 0.0371 (15.0); 0.0263 (0.6) I-067: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.3181 (6.0); 7.6233 (4.5); 7.6065 (3.3); 7.5784 (0.3); 7.3678 (2.4); 7.3120 (1.0); 7.2988 (8.6); 7.2861 (1.1); 7.2741 (0.6); 7.0082 (2.3); 6.9827 (2.8); 6.9230 (2.9); 6.7174 (1.3); 6.6922 (1.1); 6.1085 (1.9); 5.9760 (0.7); 5.9705 (0.7); 5.9543 (0.8); 5.9489 (0.7); 5.8177 (0.7); 5.8124 (0.7); 5.7961 (0.7); 5.7905 (0.7); 4.3479 (1.1); 4.3378 (1.2); 4.3130 (1.4); 4.3029 (1.3); 3.9505 (0.5); 3.9351 (0.7); 3.9288 (0.7); 3.9239 (0.7); 3.9177 (0.8); 3.9075 (0.6); 3.9014 (0.7); 3.8941 (0.6); 3.8816 (2.2); 3.8606 (0.9); 3.8468 (1.6); 3.8257 (1.0); 3.0646 (0.9); 3.0499 (1.0); 3.0191 (1.3); 3.0040 (1.2); 2.7731 (0.8); 2.7670 (0.9); 2.7404 (0.8); 2.7343 (0.9); 2.7287 (0.8); 2.7218 (0.8); 2.6952 (0.6); 2.6889 (0.7); 2.3062 (16.0); 2.1889 (14.8); 1.8262 (2.6); 1.8148 (3.1); 1.8044 (2.7); 1.7930 (3.1); 1.7451 (2.7); 1.7337 (3.2); 1.7233 (2.7); 1.7120 (3.0); 1.6043 (2.4); 1.3030 (1.1); 0.9422 (0.4); 0.9204 (1.1); 0.8972 (0.4); 0.1091 (0.4); 0.0384 (9.3); 0.0276 (0.4) I-068: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9029 (8.4); 7.5863 (4.4); 7.5690 (4.7); 7.3267 (2.5); 7.2985 (11.1); 7.2792 (1.0); 7.2707 (1.0); 7.2626 (1.6); 7.2564 (1.3); 7.2491 (0.9); 7.2409 (0.7); 6.9986 (2.5); 6.9731 (2.9); 6.9166 (3.0); 6.7121 (1.6); 6.6866 (1.4); 6.1474 (1.9); 4.3254 (1.1); 4.3158 (1.3); 4.2907 (1.4); 4.2806 (1.4); 4.2141 (0.6); 3.9315 (0.6); 3.9194 (0.8); 3.9096 (0.7); 3.8986 (0.8); 3.8914 (0.6); 3.8825 (0.7); 3.8749 (0.6); 3.8613 (2.5); 3.8403 (1.0); 3.8264 (1.9); 3.8053 (1.2); 3.0466 (1.0); 3.0320 (1.0); 3.0012 (1.4); 2.9860 (1.3); 2.7576 (1.4); 2.7251 (1.4); 2.7123 (1.2); 2.6793 (1.0); 2.2974 (16.0); 2.1858 (15.1); 2.1659 (0.9); 2.1568 (1.8); 2.1455 (0.7); 2.1397 (0.9); 2.1302 (1.0); 2.1128 (0.6); 1.6075 (3.2); 1.2927 (0.4); 1.1820 (0.4); 1.1597 (1.7); 1.1513 (3.9); 1.1451 (3.4); 1.1346 (5.3); 1.1286 (5.4); 1.1211 (1.9); 1.1088 (2.1); 1.1021 (3.1); 1.0932 (1.7); 1.0724 (0.4); 0.7120 (0.4); 0.7038 (0.6); 0.6948 (0.5); 0.6822 (0.6); 0.6737 (0.9); 0.6650 (0.6); 0.6519 (0.4); 0.6453 (0.4); 0.6200 (0.3); 0.6108 (0.6); 0.6007 (0.5); 0.5912 (0.7); 0.5835 (0.4); 0.5182 (0.4); 0.5061 (0.4); 0.0483 (0.5); 0.0376 (13.4); 0.0268 (0.6); −0.1248 (0.4) I-069: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.2219 (1.7); 7.6115 (1.1); 7.6089 (1.1); 7.6028 (0.5); 7.5982 (0.5); 7.5898 (0.6); 7.3508 (0.6); 7.2988 (2.8); 6.9956 (0.6); 6.9702 (0.7); 6.9213 (0.7); 6.7079 (0.4); 6.0933 (0.5); 4.2941 (0.3); 4.2841 (0.3); 3.8595 (0.5); 3.8246 (0.4); 2.2962 (3.6); 2.1896 (3.3); 1.6004 (2.6); 0.3194 (0.5); 0.3125 (0.8); 0.3008 (16.0); 0.2895 (0.8); 0.0379 (3.3) I-070: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.1126 (16.0); 7.5854 (1.0); 7.5708 (10.5); 7.5561 (4.7); 7.5405 (1.5); 7.5325 (0.4); 7.2596 (10.0); 7.2541 (6.1); 7.2374 (2.6); 7.2335 (3.2); 7.2235 (2.6); 7.2193 (3.4); 7.2153 (1.9); 7.2024 (0.4); 7.1703 (1.5); 7.1560 (5.0); 7.1499 (9.7); 7.1402 (17.4); 7.1342 (10.4); 7.1267 (6.0); 6.0810 (3.7); 4.2867 (2.6); 4.2799 (2.9); 4.2649 (3.0); 4.2582 (3.2); 3.9225 (0.4); 3.9099 (1.2); 3.9059 (1.3); 3.9022 (1.7); 3.8992 (1.6); 3.8962 (1.6); 3.8899 (1.9); 3.8863 (1.5); 3.8824 (1.4); 3.8698 (0.7); 3.8137 (4.1); 3.8011 (3.2); 3.7919 (3.8); 3.7793 (3.0); 3.0428 (2.6); 3.0333 (2.7); 3.0158 (3.1); 3.0064 (3.1); 2.7014 (3.3); 2.6814 (3.3); 2.6744 (3.1); 2.6544 (2.8); 2.1659 (7.3); 1.5873 (0.8); 0.0062 (0.4); −0.0002 (9.4); −0.0065 (0.7) I-071: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.6492 (8.8); 7.4138 (1.0); 7.3877 (2.7); 7.3712 (1.9); 7.3457 (2.3); 7.3199 (1.0); 7.2989 (4.7); 7.1656 (1.7); 7.1397 (1.6); 7.1254 (4.0); 7.0988 (3.6); 7.0341 (4.4); 7.0170 (1.7); 4.3139 (1.9); 4.2769 (2.3); 4.1709 (0.7); 4.1471 (0.7); 4.0378 (0.7); 4.0150 (1.3); 3.9878 (0.7); 3.9066 (1.5); 3.8989 (1.5); 3.8695 (1.4); 3.8619 (1.3); 3.2617 (9.0); 3.0687 (2.2); 3.0572 (2.0); 3.0402 (2.8); 3.0116 (0.4); 2.3339 (15.3); 2.2980 (0.4); 2.2414 (16.0); 2.0818 (3.7); 1.7418 (0.4); 1.3197 (1.0); 1.2957 (2.7); 1.2722 (0.9); 0.0379 (4.3) I-072: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.5830 (1.1); 7.5616 (3.2); 7.5398 (0.4); 7.4678 (1.5); 7.4343 (0.7); 7.4255 (1.1); 7.4183 (0.6); 7.4112 (0.4); 7.4035 (0.6); 7.3967 (0.4); 7.2990 (4.8); 7.0362 (2.8); 7.0109 (2.2); 6.9696 (1.2); 6.9443 (0.6); 5.3365 (0.9); 4.9700 (1.1); 4.7061 (0.4); 4.6931 (0.5); 4.6772 (0.4); 4.6697 (0.8); 4.6555 (1.5); 4.6411 (0.8); 4.6183 (0.7); 4.6032 (1.4); 4.5885 (0.8); 4.5821 (0.4); 4.5687 (0.4); 4.5652 (0.5); 4.5522 (0.3); 4.1810 (0.4); 4.1720 (0.8); 4.1465 (1.0); 4.1376 (0.6); 3.9367 (0.5); 3.9277 (0.5); 3.9183 (0.6); 3.9090 (0.8); 3.9015 (1.4); 3.8674 (1.0); 3.8495 (0.6); 3.8008 (2.1); 3.7866 (3.1); 3.7715 (1.8); 3.4187 (16.0); 3.0154 (0.4); 2.9970 (0.4); 2.9696 (0.9); 2.9509 (0.8); 2.8856 (0.7); 2.8570 (0.7); 2.8391 (0.5); 2.8111 (0.4); 2.3497 (0.5); 2.3172 (12.2); 2.0405 (9.2); 1.6172 (1.0); 0.0384 (5.0) I-073: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.4004 (0.4); 8.3143 (5.2); 7.7190 (0.5); 7.6709 (0.5); 7.6603 (4.7); 7.6576 (4.7); 7.6409 (3.1); 7.6136 (0.4); 7.3830 (2.7); 7.3483 (0.3); 7.3358 (1.2); 7.3273 (1.4); 7.3170 (1.7); 7.3101 (1.6); 7.2991 (10.8); 7.0081 (2.5); 6.9826 (3.0); 6.9222 (3.0); 6.6987 (1.6); 6.6735 (1.4); 6.2869 (2.1); 4.3887 (1.1); 4.3789 (1.2); 4.3536 (1.4); 4.3439 (1.4); 3.9680 (0.5); 3.9510 (0.7); 3.9347 (0.8); 3.9185 (0.7); 3.9113 (0.6); 3.8954 (2.3); 3.8741 (1.0); 3.8604 (1.8); 3.8390 (1.1); 3.0893 (1.0); 3.0747 (1.0); 3.0439 (1.4); 3.0290 (1.2); 2.7679 (1.4); 2.7350 (1.3); 2.7227 (1.2); 2.6892 (1.0); 2.3320 (0.8); 2.3135 (16.0); 2.2506 (0.6); 2.1783 (15.0); 1.7670 (0.5); 1.2922 (1.5); 0.0374 (10.2); 0.0266 (0.5) I-074: ¹H-NMR(499.9 MHz, d₆-DMSO): δ = 8.3436 (2.3); 7.8313 (6.3); 7.7605 (2.6); 7.7368 (2.3); 7.7305 (2.2); 7.7216 (2.1); 7.6751 (2.8); 7.6596 (1.7); 6.9652 (2.4); 6.7853 (2.3); 5.0047 (1.3); 4.1443 (1.0); 4.1364 (1.1); 4.1225 (1.2); 4.1146 (1.1); 3.5631 (1.2); 3.5513 (1.2); 3.5413 (1.2); 3.5295 (1.1); 3.3168 (36.0); 2.6156 (16.0); 2.5116 (5.9); 2.5083 (12.5); 2.5047 (17.4); 2.5012 (13.2); 2.4978 (6.8); 2.1474 (1.4); 2.1378 (12.0); 2.0675 (1.1); 1.9924 (0.8); 1.8396 (11.8); 1.1789 (0.4) I-075: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9550 (5.2); 7.2987 (14.4); 7.1410 (0.6); 7.1136 (3.4); 7.0876 (3.4); 7.0603 (3.4); 7.0551 (2.9); 7.0424 (1.1); 7.0371 (1.4); 7.0157 (0.6); 7.0099 (0.6); 6.8645 (0.8); 6.8584 (0.7); 6.8380 (1.2); 6.8166 (0.6); 6.8112 (0.6); 6.6263 (1.3); 6.6203 (1.3); 6.6002 (1.2); 6.5943 (1.2); 6.2336 (1.2); 5.3369 (9.3); 4.2320 (0.9); 4.2212 (1.0); 4.1959 (1.1); 4.1851 (1.2); 4.0257 (0.4); 4.0161 (0.5); 3.9963 (0.6); 3.9868 (0.6); 3.9778 (0.4); 3.9692 (0.3); 3.9173 (1.5); 3.8994 (1.0); 3.8813 (1.2); 3.8635 (0.9); 3.1906 (0.8); 3.1743 (0.8); 3.1460 (1.1); 3.1295 (1.1); 2.9936 (0.6); 2.9215 (1.6); 2.8912 (1.1); 2.8767 (0.9); 2.8464 (0.8); 2.7107 (0.5); 2.6723 (16.0); 2.1517 (0.4); 2.1406 (0.5); 2.1234 (1.0); 2.1061 (0.6); 2.0951 (0.6); 2.0784 (0.3); 1.7846 (0.6); 1.7735 (0.6); 1.7569 (1.1); 1.7401 (0.7); 1.7289 (0.6); 1.7124 (0.4); 1.6119 (1.3); 1.2967 (0.4); 1.0878 (0.7); 1.0748 (1.3); 1.0677 (1.8); 1.0598 (1.2); 1.0547 (1.2); 1.0460 (1.5); 1.0395 (1.8); 1.0264 (1.0); 0.9577 (2.2); 0.9517 (2.5); 0.9295 (2.4); 0.9237 (2.4); 0.8987 (0.4); 0.8328 (0.8); 0.8258 (0.9); 0.8167 (1.8); 0.8094 (1.8); 0.8018 (2.0); 0.7942 (1.4); 0.7838 (0.7); 0.6283 (0.3); 0.6231 (0.4); 0.6118 (0.3); 0.6062 (0.3); 0.6010 (0.4); 0.5918 (1.0); 0.5888 (1.0); 0.5752 (1.0); 0.5712 (1.1); 0.5644 (0.9); 0.5580 (1.2); 0.5473 (0.8); 0.5414 (1.1); 0.5334 (0.4); 0.5166 (0.3); 0.1075 (2.0); 0.0484 (0.5); 0.0377 (16.4); 0.0267 (0.7) I-076: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.4211 (2.5); 7.4141 (2.6); 7.2989 (14.2); 7.2019 (2.0); 7.1745 (2.8); 7.1640 (0.4); 7.1461 (2.4); 7.1400 (1.7); 7.1369 (1.8); 7.1332 (1.6); 7.1208 (3.3); 7.0604 (1.7); 7.0534 (1.7); 7.0331 (1.1); 7.0261 (1.2); 6.8688 (0.6); 6.8595 (0.6); 6.8465 (1.2); 6.8348 (0.8); 6.8277 (0.5); 6.8143 (0.5); 5.3381 (0.4); 4.8325 (1.0); 4.8241 (1.0); 4.1418 (0.4); 4.1330 (0.9); 4.1064 (1.1); 4.1000 (1.4); 4.0924 (0.9); 4.0759 (0.8); 4.0655 (0.8); 4.0468 (1.9); 4.0140 (0.8); 4.0031 (0.4); 3.2014 (0.4); 3.1833 (0.4); 3.1561 (1.2); 3.1388 (1.2); 3.1158 (1.1); 3.0879 (1.0); 3.0700 (0.4); 3.0434 (0.4); 2.5696 (16.0); 2.1117 (0.4); 2.1008 (0.5); 2.0828 (1.3); 2.0663 (0.6); 2.0555 (0.5); 1.5887 (7.7); 1.2970 (0.6); 1.0865 (0.4); 1.0813 (0.4); 1.0716 (1.4); 1.0634 (1.6); 1.0533 (0.8); 1.0483 (0.7); 1.0428 (1.4); 1.0354 (1.7); 1.0258 (0.5); 1.0203 (0.5); 0.8248 (0.5); 0.8185 (0.5); 0.8086 (2.2); 0.8020 (2.1); 0.7916 (2.2); 0.7854 (2.0); 0.7743 (0.4); 0.7687 (0.4); 0.1073 (4.8); 0.0485 (0.6); 0.0377 (18.4); 0.0268 (0.7) I-077: ¹H-NMR(400.1 MHz, d₆-DMSO): δ = 10.9075 (2.2); 8.1383 (6.9); 7.9621 (2.6); 7.3552 (1.5); 7.3357 (3.0); 7.3160 (1.9); 7.2458 (2.4); 7.2270 (2.8); 7.0556 (1.9); 7.0517 (2.1); 7.0293 (2.7); 7.0242 (2.8); 7.0014 (10.7); 6.9806 (1.9); 5.0954 (1.2); 5.0818 (1.3); 5.0642 (1.4); 5.0507 (1.2); 3.3154 (3.8); 2.8997 (16.0); 2.7410 (14.5); 2.6392 (1.1); 2.6255 (1.2); 2.5980 (1.7); 2.5844 (1.6); 2.5135 (13.0); 2.5095 (16.6); 2.4033 (1.6); 2.3720 (1.8); 2.3622 (1.5); 2.3306 (1.6); 2.3120 (15.5); 2.2578 (14.4); 2.2206 (0.4); 1.9992 (0.4); 1.9862 (0.8); 1.9775 (1.0); 1.9656 (1.7); 1.9530 (1.0); 1.9448 (0.9); 1.9322 (0.5); 1.0042 (1.0); 0.9932 (2.9); 0.9879 (3.2); 0.9724 (3.0); 0.9672 (3.0); 0.9569 (1.2); 0.7039 (1.2); 0.6930 (3.5); 0.6888 (3.5); 0.6809 (3.3); 0.6765 (3.6); 0.6650 (1.0) I-078: ¹H-NMR(499.9 MHz, CDCl3): δ = 9.1273 (1.6); 8.6675 (0.5); 8.2413 (8.7); 8.0140 (1.6); 7.3345 (0.4); 7.3271 (1.8); 7.3187 (0.4); 7.3113 (3.6); 7.2954 (2.2); 7.2592 (12.4); 7.0889 (2.4); 7.0735 (3.2); 7.0472 (0.3); 7.0429 (0.3); 7.0222 (4.1); 7.0040 (2.0); 7.0012 (2.2); 6.9991 (2.0); 6.9831 (1.4); 6.9558 (1.5); 6.9541 (1.6); 6.9510 (1.7); 6.9493 (1.6); 6.9396 (1.4); 6.9379 (1.4); 6.9348 (1.6); 6.9331 (1.4); 6.8813 (2.2); 6.8774 (2.9); 6.8733 (1.9); 4.0911 (0.4); 4.0795 (0.7); 4.0749 (0.6); 4.0684 (0.9); 4.0635 (0.8); 4.0571 (0.8); 4.0523 (0.8); 4.0457 (0.5); 4.0411 (0.7); 4.0295 (0.4); 3.2083 (1.2); 3.1961 (1.2); 3.1807 (1.4); 3.1686 (1.3); 2.9531 (14.4); 2.8806 (12.2); 2.8801 (12.4); 2.8608 (1.5); 2.8495 (1.4); 2.8332 (1.2); 2.5865 (1.5); 2.5755 (1.6); 2.5531 (2.0); 2.5421 (1.9); 2.3698 (2.6); 2.3571 (16.0); 2.3476 (2.4); 2.3364 (1.8); 2.3140 (2.4); 2.3064 (14.3); 2.2360 (0.9); 2.1111 (0.8); 2.0026 (0.5); 1.9395 (0.5); 1.9294 (0.9); 1.9228 (0.9); 1.9196 (0.6); 1.9127 (1.6); 1.9058 (0.6); 1.9026 (0.9); 1.8959 (0.8); 1.8858 (0.5); 1.5905 (0.6); 1.0039 (1.3); 0.9944 (2.8); 0.9908 (3.0); 0.9872 (1.6); 0.9816 (1.7); 0.9776 (2.9); 0.9740 (2.7); 0.9648 (1.3); 0.7282 (1.6); 0.7187 (3.7); 0.7154 (3.2); 0.7089 (2.9); 0.7056 (3.6); 0.6958 (1.1); 0.0063 (0.8); −0.0002 (15.6); −0.0069 (0.5) I-079: ¹H-NMR(300.1 MHz, d₆-DMSO): δ = 7.7389 (0.7); 7.7172 (8.1); 7.6852 (2.8); 7.6763 (3.1); 7.6587 (2.5); 7.6327 (1.1); 7.5939 (1.8); 7.5678 (1.1); 7.5424 (3.1); 7.5357 (3.3); 7.4345 (2.4); 7.4068 (3.1); 7.2348 (2.0); 7.2277 (1.9); 7.2073 (1.6); 7.2002 (1.5); 6.8128 (2.0); 6.8026 (1.9); 4.2243 (0.4); 4.2057 (0.7); 4.1831 (1.0); 4.1641 (1.3); 4.1413 (1.2); 4.1289 (0.8); 4.1130 (0.8); 4.0010 (0.5); 3.9780 (1.2); 3.9567 (0.8); 3.9367 (0.9); 3.9133 (0.4); 3.3255 (1.4); 3.1423 (0.8); 3.1192 (0.8); 3.0961 (1.1); 3.0734 (1.0); 2.8798 (1.1); 2.8554 (1.1); 2.8339 (0.8); 2.8093 (0.8); 2.5810 (16.0); 2.5092 (5.3); 2.5034 (6.9); 2.4976 (4.9); 2.0613 (0.6); 2.0384 (1.0); 2.0124 (1.2); 1.9890 (1.1); −0.0005 (5.2) I-080: ¹H-NMR(400.1 MHz, CDCl3): δ = 8.0017 (0.6); 7.9803 (0.6); 7.9065 (5.3); 7.6479 (0.7); 7.5681 (0.5); 7.5473 (2.6); 7.5320 (7.5); 7.5257 (6.6); 7.5092 (4.1); 7.5041 (5.5); 7.4565 (1.2); 7.4351 (3.8); 7.3813 (1.8); 7.3755 (2.2); 7.3560 (6.6); 7.3395 (3.3); 7.3346 (4.2); 7.2669 (2.4); 7.2612 (5.3); 7.2508 (0.8); 6.7548 (2.8); 5.6001 (0.5); 3.8279 (0.6); 3.8124 (2.1); 3.7967 (2.2); 3.7863 (0.7); 3.7812 (0.8); 3.2369 (1.2); 2.7506 (0.4); 2.6986 (16.0); 2.6095 (2.1); 1.6808 (0.4); 1.6203 (1.8); 1.6030 (2.1); 1.4230 (1.7); 1.3909 (0.5); 1.3735 (0.5); 1.3320 (0.9); 1.2571 (8.3); 1.1584 (8.1); 1.1427 (8.4); 1.0319 (0.5); 1.0155 (0.5); 0.9945 (0.4); 0.9782 (0.4); 0.8950 (1.0); 0.8801 (1.7); 0.8700 (1.3); 0.8629 (1.3); 0.0715 (0.5); 0.0057 (2.7); −0.0002 (6.1) I-081: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.0074 (5.1); 7.5465 (0.3); 7.5308 (1.4); 7.5168 (4.0); 7.5029 (0.3); 7.4219 (1.8); 7.3604 (0.7); 7.3558 (1.3); 7.3515 (0.8); 7.3479 (0.5); 7.3460 (0.6); 7.3409 (1.1); 7.3351 (3.6); 7.3313 (1.2); 7.3219 (1.5); 7.3181 (4.7); 7.3132 (0.6); 7.2614 (4.1); 7.2306 (0.7); 7.2261 (4.4); 7.2224 (1.3); 7.2128 (1.2); 7.2092 (3.2); 7.2043 (0.4); 6.5340 (0.9); 6.5254 (0.9); 4.5924 (1.1); 4.5863 (1.3); 4.5836 (1.3); 4.5774 (1.1); 4.1824 (1.0); 4.1765 (1.0); 4.1695 (1.0); 4.1635 (1.0); 2.6861 (16.0); 1.9977 (0.5); 1.5905 (0.3); 1.0315 (7.0); 1.0186 (6.9); −0.0002 (4.9) I-082: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.6780 (3.4); 8.6717 (3.5); 8.3307 (0.3); 8.3202 (3.4); 8.3122 (3.5); 8.1643 (8.6); 7.6383 (2.3); 7.6308 (3.6); 7.6240 (2.3); 7.2991 (5.3); 6.9977 (2.4); 6.9721 (3.0); 6.9485 (2.9); 6.7777 (1.6); 6.7523 (1.2); 5.9734 (1.8); 4.3550 (1.1); 4.3453 (1.3); 4.3197 (1.4); 4.3098 (1.4); 3.9450 (0.5); 3.9390 (0.5); 3.9297 (0.7); 3.9234 (0.7); 3.9118 (0.8); 3.9051 (0.6); 3.9008 (0.6); 3.8952 (0.6); 3.8894 (0.5); 3.8798 (0.4); 3.8608 (2.4); 3.8396 (1.2); 3.8254 (1.9); 3.8042 (1.3); 3.0706 (1.0); 3.0555 (1.0); 3.0251 (1.3); 3.0096 (1.3); 2.7437 (1.5); 2.7102 (1.4); 2.6982 (1.2); 2.6643 (1.1); 2.4286 (0.4); 2.3063 (16.0); 2.2424 (14.7); 2.0427 (4.5); 1.6422 (0.9); 0.0361 (6.4) I-083: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.2832 (2.8); 8.2780 (2.8); 8.1440 (7.0); 7.7726 (3.3); 7.7673 (3.1); 7.2602 (12.4); 6.9574 (2.6); 6.9422 (2.9); 6.9081 (3.4); 6.7340 (1.9); 6.7191 (1.6); 5.8274 (2.2); 4.3260 (1.4); 4.3195 (1.4); 4.3043 (1.5); 4.2978 (1.5); 3.9177 (0.7); 3.9097 (1.0); 3.8978 (1.0); 3.8936 (0.8); 3.8900 (0.7); 3.8265 (1.9); 3.8137 (1.5); 3.8047 (1.7); 3.7920 (1.3); 3.0301 (1.2); 3.0210 (1.2); 3.0026 (1.4); 2.9934 (1.3); 2.6971 (1.5); 2.6764 (1.5); 2.6696 (1.4); 2.6489 (1.2); 2.3270 (0.3); 2.3149 (0.3); 2.3035 (0.6); 2.2742 (16.0); 2.1789 (15.2); 1.5479 (12.8); 1.2734 (0.6); 1.2608 (0.7); −0.0002 (15.1) I-084: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.5701 (2.5); 7.5638 (2.6); 7.2989 (11.2); 7.2116 (1.0); 7.2052 (0.9); 7.1845 (1.9); 7.1781 (2.0); 7.1451 (2.7); 7.1356 (4.8); 7.1199 (3.2); 7.1086 (1.7); 6.8693 (0.6); 6.8595 (0.6); 6.8473 (1.1); 6.8359 (0.9); 6.8269 (0.5); 6.8150 (0.5); 4.8462 (1.1); 4.8382 (1.1); 4.1687 (0.4); 4.1448 (0.5); 4.1366 (0.4); 4.1283 (0.9); 4.1219 (0.4); 4.1004 (1.3); 4.0959 (1.4); 4.0879 (0.9); 4.0778 (0.8); 4.0713 (0.7); 4.0608 (0.9); 4.0439 (1.9); 4.0126 (0.8); 4.0011 (0.4); 3.1868 (0.4); 3.1689 (0.4); 3.1411 (1.2); 3.1243 (1.2); 3.1026 (1.0); 3.0746 (1.0); 3.0571 (0.4); 3.0301 (0.4); 2.5670 (16.0); 2.1168 (0.4); 2.1058 (0.5); 2.0885 (1.0); 2.0816 (2.8); 2.0713 (0.6); 2.0605 (0.5); 1.5965 (10.9); 1.3201 (0.5); 1.2963 (1.1); 1.2725 (0.4); 1.0906 (0.3); 1.0820 (0.4); 1.0744 (1.3); 1.0658 (1.7); 1.0456 (1.4); 1.0382 (1.8); 1.0313 (0.6); 1.0225 (0.4); 0.9969 (0.3); 0.9726 (0.5); 0.8277 (0.5); 0.8188 (0.4); 0.8108 (2.1); 0.8038 (1.7); 0.7943 (2.0); 0.7873 (1.8); 0.7790 (0.4); 0.7706 (0.4); 0.1071 (3.8); 0.0482 (0.4); 0.0373 (11.6); 0.0264 (0.4) I-085: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.2989 (13.4); 7.1569 (0.4); 7.1359 (1.8); 7.1291 (4.2); 7.1121 (4.1); 7.1025 (4.9); 7.0859 (0.5); 6.8599 (0.6); 6.8513 (0.7); 6.8374 (1.2); 6.8242 (2.2); 6.8190 (1.9); 6.8059 (0.7); 6.7986 (1.2); 6.7926 (1.2); 4.8268 (1.2); 4.8173 (1.2); 4.1651 (0.8); 4.1548 (1.0); 4.1466 (0.5); 4.1289 (1.2); 4.1188 (1.5); 4.0785 (0.4); 4.0633 (0.6); 4.0486 (0.7); 4.0379 (0.6); 4.0201 (0.4); 3.9935 (1.4); 3.9792 (0.8); 3.9575 (0.9); 3.9432 (0.7); 3.1701 (0.6); 3.1519 (0.6); 3.1249 (1.3); 3.1066 (1.2); 3.0459 (1.2); 3.0180 (1.2); 3.0009 (0.7); 2.9728 (0.6); 2.5597 (16.0); 2.1279 (0.5); 2.1167 (0.5); 2.0996 (1.0); 2.0827 (3.0); 2.0715 (0.6); 1.8776 (0.5); 1.8662 (0.6); 1.8495 (1.1); 1.8328 (0.6); 1.8216 (0.6); 1.5941 (13.3); 1.3208 (0.5); 1.2970 (1.1); 1.2731 (0.4); 1.0781 (0.4); 1.0625 (1.8); 1.0558 (2.0); 1.0344 (2.1); 1.0273 (2.0); 1.0211 (2.1); 1.0145 (2.5); 0.9993 (1.2); 0.9927 (2.0); 0.9864 (1.8); 0.9720 (1.2); 0.8231 (0.8); 0.8090 (1.9); 0.8052 (2.0); 0.7918 (1.9); 0.7874 (1.8); 0.7708 (0.6); 0.7079 (0.9); 0.6924 (2.3); 0.6868 (2.0); 0.6762 (1.9); 0.6704 (2.4); 0.6543 (0.7); 0.1073 (1.6); 0.0486 (0.4); 0.0376 (14.2); 0.0265 (0.5) I-086: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1343 (5.8); 7.3665 (1.2); 7.3402 (2.5); 7.3138 (1.6); 7.2990 (16.2); 7.0495 (1.5); 7.0237 (1.2); 6.9870 (1.8); 6.9616 (2.2); 6.9259 (2.2); 6.8496 (1.0); 6.8442 (1.2); 6.8224 (0.8); 6.8173 (1.1); 6.7829 (1.7); 6.7768 (2.2); 6.7702 (1.3); 6.6910 (1.2); 6.6680 (1.0); 6.2783 (1.4); 4.2975 (0.7); 4.2887 (1.0); 4.2634 (1.1); 4.2545 (0.9); 4.1962 (0.3); 4.1723 (1.0); 4.1485 (1.0); 4.1247 (0.4); 3.8854 (0.5); 3.8807 (0.5); 3.8705 (0.5); 3.8644 (0.6); 3.8568 (0.5); 3.8427 (2.1); 3.8228 (0.5); 3.8088 (1.4); 3.7879 (0.8); 3.0419 (0.7); 3.0268 (0.6); 2.9968 (1.0); 2.9810 (1.0); 2.7490 (0.9); 2.7176 (0.9); 2.7111 (0.6); 2.7035 (0.9); 2.6721 (0.8); 2.3334 (0.4); 2.3164 (0.5); 2.2986 (11.7); 2.2185 (10.9); 2.0843 (4.6); 1.9800 (0.5); 1.9690 (0.6); 1.9522 (1.1); 1.9355 (0.6); 1.9243 (0.6); 1.9076 (0.3); 1.5911 (16.0); 1.3221 (1.2); 1.2983 (2.3); 1.2745 (1.1); 1.0762 (0.7); 1.0609 (1.8); 1.0543 (2.0); 1.0395 (1.0); 1.0326 (2.0); 1.0262 (1.8); 1.0117 (0.9); 0.7767 (0.8); 0.7613 (2.3); 0.7556 (2.1); 0.7452 (2.0); 0.7393 (2.4); 0.7234 (0.8); 0.0494 (0.6); 0.0385 (19.1); 0.0278 (0.9) I-087: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9885 (5.2); 7.5896 (1.3); 7.5673 (4.1); 7.5456 (0.4); 7.4894 (1.9); 7.4509 (0.8); 7.4423 (1.4); 7.4349 (0.8); 7.4201 (0.8); 7.4127 (0.4); 7.2990 (8.7); 7.2289 (2.1); 7.1343 (1.1); 7.1289 (1.0); 7.1070 (1.2); 7.1020 (1.2); 6.8063 (2.5); 6.7790 (2.1); 6.1439 (1.5); 4.7393 (0.6); 4.7250 (0.8); 4.7181 (0.8); 4.7142 (0.7); 4.7033 (0.7); 4.6331 (2.1); 4.6042 (4.0); 4.5747 (2.4); 4.3707 (0.9); 4.3590 (0.8); 4.3339 (1.0); 4.3219 (0.9); 4.1698 (0.5); 4.1460 (0.5); 4.1226 (0.3); 4.1011 (0.4); 3.7539 (1.4); 3.7284 (1.4); 3.7170 (1.3); 3.6916 (1.2); 3.2304 (0.3); 3.2073 (0.7); 3.1787 (1.2); 3.1683 (0.7); 3.1494 (0.7); 3.1386 (1.2); 3.1099 (0.6); 3.0867 (0.3); 2.7304 (16.0); 2.0821 (3.4); 1.6084 (2.3); 1.3202 (0.7); 1.2963 (1.5); 1.2725 (0.6); 0.9726 (0.6); 0.1075 (4.1); 0.0483 (0.4); 0.0373 (10.6); 0.0267 (0.4) I-088: ¹H-NMR(400.1 MHz, CDCl3): δ = 8.7679 (3.6); 8.7592 (3.8); 7.6044 (0.5); 7.5847 (2.2); 7.5690 (6.7); 7.4657 (4.0); 7.4341 (2.1); 7.4293 (2.1); 7.4169 (1.7); 7.3367 (4.8); 7.3255 (5.0); 7.2639 (4.3); 7.2599 (4.5); 6.9715 (4.5); 6.8823 (1.8); 6.8631 (2.9); 6.8025 (3.4); 6.7835 (2.2); 5.2996 (0.5); 5.2958 (0.5); 4.6223 (3.1); 3.8036 (1.5); 3.7763 (2.0); 3.6596 (1.3); 3.6528 (1.3); 3.5978 (1.9); 3.5870 (1.4); 3.5704 (1.5); 3.5598 (1.2); 2.7710 (1.0); 2.7589 (1.1); 2.7363 (1.6); 2.7239 (1.6); 2.6000 (1.5); 2.5767 (1.5); 2.5666 (1.2); 2.5424 (1.1); 2.2787 (15.7); 2.1913 (16.0); 2.0922 (0.4); 1.6137 (0.8); 1.2585 (0.5); 0.0038 (4.2); −0.0002 (4.4) I-089: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.2317 (8.4); 7.2989 (10.4); 7.1428 (0.8); 7.1390 (0.8); 7.1162 (1.9); 7.1127 (2.0); 7.0896 (1.4); 7.0863 (1.6); 7.0318 (4.7); 7.0068 (4.3); 6.9938 (2.1); 6.9820 (1.0); 6.9761 (1.1); 6.9714 (2.2); 6.9345 (2.0); 6.9117 (3.0); 6.8689 (1.0); 6.8634 (1.0); 6.8422 (1.8); 6.8207 (0.9); 6.8154 (0.8); 6.7119 (1.6); 6.6870 (1.3); 6.2528 (4.9); 6.1934 (2.8); 5.6604 (3.2); 5.6232 (3.1); 5.3373 (0.8); 4.3082 (1.0); 4.2994 (1.4); 4.2740 (1.5); 4.2651 (1.2); 3.9212 (0.7); 3.9151 (0.8); 3.9049 (0.7); 3.8994 (0.8); 3.8931 (0.7); 3.8772 (2.9); 3.8574 (0.7); 3.8433 (2.0); 3.8227 (1.1); 3.0533 (0.9); 3.0380 (0.9); 3.0087 (1.4); 2.9921 (1.3); 2.8035 (1.2); 2.7729 (1.2); 2.7584 (1.1); 2.7276 (1.0); 2.3161 (16.0); 2.1821 (15.1); 2.1512 (0.7); 2.1401 (0.8); 2.1229 (1.4); 2.1055 (0.9); 2.0946 (0.8); 2.0775 (0.4); 1.6227 (0.9); 1.0957 (0.9); 1.0822 (1.9); 1.0758 (2.4); 1.0710 (1.5); 1.0677 (1.5); 1.0628 (1.5); 1.0537 (2.0); 1.0475 (2.3); 1.0345 (1.2); 0.8379 (1.2); 0.8309 (1.2); 0.8219 (2.6); 0.8147 (2.4); 0.8062 (2.7); 0.7991 (1.7); 0.7888 (0.9); 0.0492 (0.4); 0.0384 (13.1); 0.0275 (0.5) I-090: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.9242 (5.2); 7.5668 (0.5); 7.5513 (1.5); 7.5358 (2.5); 7.5319 (2.2); 7.5161 (0.5); 7.4530 (1.8); 7.4096 (0.8); 7.4060 (1.2); 7.4020 (0.8); 7.3910 (0.9); 7.2613 (6.0); 6.5759 (2.5); 5.9837 (1.4); 4.7968 (0.7); 4.7942 (0.7); 4.7883 (0.8); 4.7856 (0.8); 4.7809 (0.8); 4.7781 (0.8); 4.7722 (0.7); 4.7696 (0.7); 4.2757 (0.8); 4.2743 (0.9); 4.2673 (0.8); 4.2657 (0.9); 4.2537 (0.9); 4.2521 (1.0); 4.2451 (0.9); 4.2436 (0.9); 3.7076 (1.4); 3.6915 (1.4); 3.6855 (1.4); 3.6694 (1.3); 2.6872 (16.0); 2.3844 (11.4); 2.2880 (9.2); 2.0425 (1.3); 1.5864 (0.8); 1.2724 (0.4); 1.2581 (0.7); 1.2438 (0.3); −0.0002 (6.3) I-091: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.9085 (5.6); 7.5517 (0.6); 7.5361 (1.7); 7.5210 (3.1); 7.5021 (0.6); 7.4658 (1.9); 7.4195 (0.8); 7.4158 (1.3); 7.4117 (0.8); 7.4044 (0.6); 7.4009 (0.9); 7.3973 (0.6); 7.2655 (1.2); 6.8568 (2.2); 6.8499 (2.3); 6.6336 (1.5); 6.6314 (1.6); 6.6291 (1.2); 6.6267 (1.5); 6.6245 (1.5); 6.3102 (1.3); 5.2913 (3.7); 4.9634 (0.6); 4.9601 (0.7); 4.9555 (0.7); 4.9507 (0.9); 4.9461 (0.7); 4.9415 (0.7); 4.9382 (0.6); 4.3320 (1.0); 4.3254 (0.9); 4.3239 (1.0); 4.3111 (0.9); 4.3099 (1.1); 4.3033 (0.9); 4.3019 (1.0); 3.8426 (1.5); 3.8284 (1.5); 3.8205 (1.4); 3.8063 (1.4); 2.6695 (2.2); 2.6640 (16.0); 2.4647 (1.7); 2.4334 (8.8); 2.4316 (10.3); 2.4155 (0.4); 2.4135 (0.4); 2.0313 (0.5); −0.0002 (1.1) I-092: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.3438 (1.5); 8.3410 (1.7); 8.3345 (1.6); 8.3317 (1.7); 7.9737 (5.2); 7.9564 (1.6); 7.9536 (1.7); 7.9406 (1.6); 7.9378 (1.7); 7.4972 (3.0); 7.4869 (3.9); 7.3556 (2.0); 7.3143 (0.8); 7.3093 (0.8); 7.3052 (1.1); 7.3014 (1.0); 7.2962 (0.8); 7.2913 (0.6); 7.2654 (3.9); 7.2306 (4.6); 6.9768 (1.5); 6.9674 (1.6); 6.9610 (1.6); 6.9516 (1.5); 6.2094 (1.7); 5.0486 (0.7); 5.0458 (0.7); 5.0406 (0.8); 5.0375 (0.9); 5.0338 (0.9); 5.0306 (0.8); 5.0254 (0.8); 5.0225 (0.8); 4.3966 (1.0); 4.3885 (1.0); 4.3745 (1.1); 4.3664 (1.0); 4.1387 (1.1); 4.1244 (3.3); 4.1101 (3.4); 4.0959 (1.2); 4.0372 (1.4); 4.0219 (1.4); 4.0151 (1.3); 3.9998 (1.2); 3.8770 (0.3); 3.8474 (16.0); 2.7143 (0.5); 2.6950 (15.6); 2.6682 (0.3); 2.0403 (13.9); 1.6847 (1.3); 1.2707 (3.7); 1.2564 (7.3); 1.2421 (3.6); −0.0002 (3.6) I-093: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9640 (5.3); 7.6306 (0.3); 7.6047 (1.3); 7.5814 (4.1); 7.5583 (0.4); 7.5255 (1.9); 7.4632 (0.8); 7.4553 (1.4); 7.4481 (0.8); 7.4423 (0.5); 7.4394 (0.5); 7.4325 (0.8); 7.4254 (0.5); 7.2989 (2.2); 6.9466 (0.4); 6.9313 (3.7); 6.9072 (3.7); 6.8921 (0.4); 6.3688 (1.0); 6.3588 (1.1); 4.0732 (0.9); 4.0620 (1.0); 4.0365 (1.4); 4.0252 (1.5); 3.9118 (1.2); 3.8980 (1.4); 3.8749 (0.8); 3.8612 (0.9); 3.6071 (0.4); 3.5922 (0.6); 3.5790 (0.8); 3.5657 (0.6); 3.5509 (0.4); 2.8386 (0.8); 2.8123 (1.4); 2.7853 (0.7); 2.6957 (16.0); 2.0252 (0.6); 2.0017 (0.7); 1.9746 (0.6); 1.9409 (0.3); 1.9232 (0.4); 1.9141 (0.7); 1.8964 (0.8); 1.8880 (0.4); 1.8690 (0.6); 1.8508 (0.3); 1.6872 (1.2); 1.2885 (0.5); 0.1067 (1.1); 0.0327 (2.2) I-094: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9769 (5.0); 7.5949 (3.5); 7.5777 (2.7); 7.3439 (1.7); 7.3415 (1.7); 7.2983 (10.5); 7.2791 (0.7); 7.2715 (0.8); 7.2606 (1.0); 7.2543 (0.9); 7.2490 (0.6); 7.2408 (0.5); 7.0949 (2.4); 7.0684 (3.8); 6.9821 (3.3); 6.9559 (2.1); 6.1624 (1.2); 4.3289 (0.8); 4.3176 (0.9); 4.2933 (1.0); 4.2819 (1.0); 3.9204 (0.4); 3.9088 (0.5); 3.9045 (0.5); 3.8983 (0.5); 3.8932 (0.5); 3.8872 (0.6); 3.8810 (0.4); 3.8761 (0.4); 3.8711 (0.4); 3.8299 (1.7); 3.8082 (0.9); 3.7944 (1.4); 3.7726 (0.9); 3.0386 (0.7); 3.0236 (0.7); 2.9939 (0.9); 2.9789 (0.8); 2.7145 (0.3); 2.7045 (1.2); 2.6770 (16.0); 2.6599 (1.0); 2.6269 (0.8); 2.2320 (10.4); 2.0445 (0.7); 1.6121 (0.4); 1.2935 (0.4); 0.0483 (0.4); 0.0375 (12.4); 0.0282 (0.4); 0.0266 (0.4) I-095: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.9642 (5.3); 7.7837 (0.6); 7.7707 (0.6); 7.7654 (1.2); 7.7525 (1.2); 7.7473 (0.7); 7.7343 (0.6); 7.5635 (0.4); 7.5480 (1.4); 7.5321 (3.5); 7.5191 (0.5); 7.5162 (0.5); 7.4751 (2.0); 7.4380 (0.4); 7.4196 (0.9); 7.4157 (1.5); 7.4117 (0.9); 7.4012 (1.0); 7.2632 (3.2); 7.1944 (1.9); 6.9462 (0.5); 6.9415 (0.6); 6.9299 (0.8); 6.9278 (1.0); 6.9134 (0.5); 6.9088 (0.6); 6.8344 (0.7); 6.8294 (0.7); 6.8173 (0.7); 6.8100 (1.0); 6.8047 (0.7); 6.7927 (0.7); 6.7876 (0.7); 5.2975 (1.5); 3.5148 (3.4); 2.6879 (16.0); 2.6071 (1.3); 2.0381 (0.5); 1.6754 (2.2); 1.6156 (2.1); 1.3315 (11.1); 1.2691 (0.3); 1.2546 (0.8); 1.2479 (6.0); 1.2424 (6.3); 0.0725 (0.6); −0.0002 (3.6) I-096: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.0252 (5.0); 7.9715 (1.2); 7.7436 (0.4); 7.5661 (0.4); 7.5534 (0.4); 7.5458 (0.6); 7.5380 (1.7); 7.5243 (4.5); 7.4259 (2.6); 7.4222 (2.7); 7.4059 (2.3); 7.3889 (2.9); 7.3798 (2.8); 7.3756 (3.3); 7.3682 (0.9); 7.3623 (1.0); 7.3575 (1.7); 7.3537 (1.6); 7.3439 (1.1); 7.3374 (1.2); 7.2619 (7.7); 7.2577 (2.2); 7.2494 (0.7); 7.2448 (1.7); 7.2404 (1.4); 7.2327 (0.4); 7.2286 (0.4); 6.5471 (1.1); 6.5374 (1.2); 6.1503 (0.4); 5.2979 (2.6); 5.2719 (1.2); 5.2659 (1.4); 5.2620 (1.4); 5.2560 (1.3); 4.9665 (0.3); 4.9603 (0.3); 4.9557 (0.3); 4.1244 (0.7); 4.1101 (0.7); 3.9345 (0.6); 3.9279 (1.1); 3.9215 (0.7); 3.9158 (0.8); 3.9092 (1.1); 3.9026 (0.7); 3.4398 (0.9); 2.6840 (16.0); 2.6409 (0.4); 2.0405 (3.6); 2.0012 (0.4); 1.6225 (0.4); 1.6166 (0.3); 1.6074 (0.5); 1.5862 (1.7); 1.5786 (1.5); 1.5710 (1.0); 1.5635 (0.9); 1.5561 (0.8); 1.5496 (0.8); 1.5422 (0.7); 1.5347 (0.6); 1.5275 (0.6); 1.2710 (1.1); 1.2566 (2.7); 1.2424 (1.0); 1.1931 (0.4); 1.1783 (0.6); 1.1742 (0.5); 1.1642 (0.6); 1.1596 (0.6); 1.1495 (0.5); 1.1456 (0.6); 1.1355 (0.3); 1.1308 (0.4); 1.0793 (0.9); 1.0611 (3.9); 1.0463 (6.5); 1.0316 (2.6); 0.9793 (0.4); 0.9594 (0.4); 0.9446 (0.6); 0.9346 (0.4); 0.9299 (0.4); 0.0710 (3.4); −0.0002 (5.8) I-097: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.7031 (2.8); 8.7014 (2.9); 8.4501 (2.3); 8.4453 (2.5); 8.1332 (8.2); 7.6000 (2.4); 7.2619 (4.0); 6.9540 (2.5); 6.9388 (2.9); 6.8914 (4.5); 6.7801 (3.1); 6.7059 (1.6); 6.6909 (1.5); 6.6689 (1.6); 5.9697 (2.0); 4.3061 (1.3); 4.2996 (1.4); 4.2844 (1.4); 4.2779 (1.5); 3.9034 (0.6); 3.8996 (0.6); 3.8955 (0.8); 3.8899 (0.7); 3.8834 (0.9); 3.8796 (0.7); 3.8760 (0.6); 3.8737 (0.6); 3.8634 (0.4); 3.8230 (2.0); 3.8104 (1.4); 3.8013 (1.8); 3.7887 (1.4); 3.0207 (1.1); 3.0113 (1.1); 2.9932 (1.3); 2.9838 (1.3); 2.7030 (1.4); 2.6827 (1.4); 2.6756 (1.3); 2.6552 (1.2); 2.3239 (0.3); 2.2999 (0.4); 2.2670 (16.0); 2.1593 (14.9); 2.0014 (1.5); 1.6105 (2.1); −0.0002 (4.5) I-098: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.4063 (8.2); 7.3548 (1.6); 7.3285 (3.5); 7.2989 (13.9); 7.0134 (3.5); 6.9876 (3.8); 6.9345 (2.9); 6.8785 (1.3); 6.8758 (1.4); 6.8706 (1.7); 6.8680 (1.7); 6.8517 (1.1); 6.8490 (1.2); 6.8439 (1.6); 6.8412 (1.5); 6.8076 (2.3); 6.8013 (3.1); 6.7947 (1.8); 6.7207 (1.6); 6.6960 (1.3); 6.2671 (2.0); 5.5662 (3.6); 5.5585 (3.7); 5.3375 (15.9); 4.4268 (3.1); 4.4191 (3.2); 4.2866 (0.8); 4.2778 (1.4); 4.2528 (1.6); 4.2447 (1.1); 4.0329 (1.5); 4.0096 (4.7); 3.9863 (4.7); 3.9631 (1.5); 3.8984 (0.6); 3.8927 (0.8); 3.8841 (0.7); 3.8771 (0.9); 3.8642 (2.4); 3.8448 (0.6); 3.8309 (2.0); 3.8104 (1.1); 3.0389 (0.8); 3.0239 (0.8); 2.9940 (1.4); 2.9779 (1.3); 2.7803 (1.1); 2.7492 (1.1); 2.7349 (1.1); 2.7109 (0.5); 2.7038 (0.9); 2.6669 (0.3); 2.3352 (0.4); 2.3060 (16.0); 2.2580 (0.4); 2.2298 (14.9); 1.9888 (0.4); 1.9720 (0.7); 1.9608 (0.8); 1.9441 (1.5); 1.9274 (0.9); 1.9161 (0.9); 1.8993 (0.5); 1.6006 (13.8); 1.4882 (5.2); 1.4650 (10.9); 1.4417 (5.1); 1.4090 (0.4); 1.3848 (0.3); 1.3610 (0.6); 1.3335 (0.4); 1.3071 (0.6); 1.2980 (0.5); 1.0584 (1.0); 1.0431 (2.5); 1.0364 (2.8); 1.0309 (1.5); 1.0217 (1.5); 1.0148 (2.8); 1.0082 (2.5); 0.9938 (1.3); 0.9855 (0.7); 0.9611 (1.3); 0.9427 (0.4); 0.9367 (0.7); 0.9203 (0.5); 0.7723 (1.3); 0.7571 (3.2); 0.7511 (2.9); 0.7408 (2.7); 0.7348 (3.4); 0.7188 (1.0); 0.1085 (0.5); 0.0494 (0.4); 0.0384 (15.6); 0.0274 (0.6) I-099: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.9843 (2.1); 7.9094 (3.3); 7.5519 (1.0); 7.5365 (1.7); 7.5329 (1.5); 7.5171 (0.4); 7.4655 (1.2); 7.4058 (0.5); 7.4023 (0.8); 7.3985 (0.5); 7.3873 (0.6); 7.2708 (1.8); 6.8574 (1.3); 6.8499 (1.7); 6.8024 (2.3); 6.7948 (1.8); 6.5050 (0.8); 4.9677 (0.4); 4.9614 (0.6); 4.9559 (0.8); 4.9505 (0.6); 4.9441 (0.4); 4.2840 (0.7); 4.2766 (0.7); 4.2618 (0.8); 4.2545 (0.7); 3.9547 (0.9); 3.9432 (0.9); 3.9326 (0.8); 3.9210 (0.8); 2.9450 (16.0); 2.8643 (14.1); 2.6741 (10.1); 1.7417 (1.6); −0.0002 (2.3) I-100: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.0006 (2.0); 7.9130 (3.1); 7.5652 (0.3); 7.5497 (0.9); 7.5339 (1.3); 7.5286 (1.2); 7.5129 (0.3); 7.4751 (1.1); 7.4264 (0.5); 7.4230 (0.7); 7.4193 (0.5); 7.4079 (0.5); 7.2735 (1.7); 6.3133 (0.8); 6.2066 (1.3); 6.2003 (1.3); 5.9351 (0.9); 5.9333 (1.0); 5.9315 (0.8); 5.9290 (0.9); 5.9272 (0.8); 4.8087 (0.4); 4.8046 (0.4); 4.8009 (0.4); 4.7959 (0.6); 4.7908 (0.4); 4.7871 (0.4); 4.7830 (0.3); 4.3383 (0.6); 4.3302 (0.6); 4.3164 (0.7); 4.3085 (0.6); 3.9721 (0.9); 3.9581 (0.9); 3.9502 (0.8); 3.9362 (0.8); 2.9506 (16.0); 2.8734 (13.8); 2.7409 (0.4); 2.6721 (9.7); 2.2084 (6.3); −0.0002 (2.2) I-101: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.0518 (2.0); 7.9603 (1.7); 7.5885 (0.6); 7.5655 (1.5); 7.5432 (0.4); 7.4724 (0.7); 7.4506 (0.4); 7.4416 (0.5); 7.4338 (0.3); 7.4200 (0.3); 7.2985 (13.4); 5.9276 (0.4); 5.8869 (0.9); 4.2664 (0.3); 4.2520 (0.3); 3.7468 (0.5); 3.7197 (0.4); 3.7103 (0.4); 3.6829 (0.4); 2.9931 (16.0); 2.9195 (14.4); 2.7836 (0.6); 2.7352 (0.5); 2.7184 (5.4); 2.6870 (0.4); 2.6780 (0.5); 2.6686 (0.5); 2.5486 (0.4); 2.5413 (0.3); 2.5078 (0.7); 2.4517 (0.3); 2.3490 (0.6); 2.3111 (0.6); 2.2906 (4.1); 2.2100 (3.4); 2.1955 (0.7); 2.1118 (1.0); 2.0652 (1.1); 1.8253 (0.9); 1.6586 (1.2); 1.2893 (0.8); 0.0353 (15.3) I-102: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.0114 (2.1); 7.9275 (3.6); 7.5675 (0.4); 7.5520 (1.1); 7.5363 (1.8); 7.5321 (1.6); 7.5164 (0.4); 7.4734 (1.5); 7.4334 (0.6); 7.4299 (0.9); 7.4262 (0.6); 7.4149 (0.7); 7.2639 (6.2); 6.2298 (0.9); 6.0954 (2.6); 4.7636 (0.4); 4.7598 (0.5); 4.7558 (0.5); 4.7507 (0.7); 4.7458 (0.5); 4.7417 (0.5); 4.7378 (0.4); 4.3296 (0.7); 4.3215 (0.7); 4.3077 (0.8); 4.2997 (0.8); 3.9367 (1.0); 3.9224 (1.0); 3.9148 (1.0); 3.9006 (0.9); 2.9545 (16.0); 2.8805 (14.2); 2.6762 (11.3); 2.1101 (7.1); 1.8848 (7.1); 1.6447 (1.0); −0.0002 (6.1); −0.0065 (0.4) I-103: ¹H-NMR(499.9 MHz, CDCl3): δ =7.9928 (2.2); 7.9231 (0.6); 7.9055 (2.8); 7.5731 (0.4); 7.5576 (1.1); 7.5416 (1.4); 7.5353 (1.6); 7.5196 (0.4); 7.4683 (1.3); 7.3982 (0.8); 7.3829 (0.6); 7.2670 (2.8); 6.7808 (2.7); 6.1278 (0.8); 4.8065 (0.4); 4.8032 (0.5); 4.7984 (0.5); 4.7947 (0.5); 4.7926 (0.6); 4.7887 (0.5); 4.7838 (0.4); 4.7805 (0.4); 4.2503 (0.6); 4.2418 (0.6); 4.2281 (0.7); 4.2197 (0.6); 3.7546 (0.8); 3.7399 (0.8); 3.7323 (0.7); 3.7177 (0.7); 2.9485 (16.0); 2.8703 (14.4); 2.6847 (9.1); 2.6795 (2.2); 2.3849 (8.9); 2.3416 (1.0); 2.3131 (0.6); 2.3113 (0.6); 2.1183 (0.8); 1.6763 (1.3); −0.0002 (3.5) I-104: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.0138 (2.1); 7.9777 (2.7); 7.5406 (1.3); 7.5236 (1.4); 7.5044 (1.1); 7.4988 (1.0); 7.4941 (2.0); 7.4926 (2.0); 7.3464 (1.1); 7.3267 (0.5); 7.3191 (0.8); 7.3146 (2.0); 7.3110 (1.7); 7.3039 (0.3); 7.2612 (9.2); 7.0707 (2.5); 7.0061 (0.9); 7.0026 (0.8); 6.9891 (0.8); 6.9856 (0.8); 6.1904 (0.9); 5.0544 (0.4); 5.0518 (0.4); 5.0462 (0.4); 5.0434 (0.4); 5.0391 (0.4); 5.0363 (0.4); 5.0307 (0.4); 4.4016 (0.5); 4.3939 (0.5); 4.3795 (0.6); 4.3718 (0.5); 4.0100 (0.7); 3.9944 (0.7); 3.9880 (0.7); 3.9724 (0.6); 3.7086 (8.5); 2.9538 (16.0); 2.8809 (14.3); 2.6967 (8.2); 2.0046 (0.4); 1.5842 (0.9); −0.0002 (11.7); −0.0067 (0.4) I-105: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.9551 (2.2); 7.8911 (3.9); 7.8852 (0.4); 7.5504 (0.3); 7.5349 (1.1); 7.5192 (1.8); 7.5143 (1.6); 7.4988 (0.5); 7.4653 (1.5); 7.4106 (0.6); 7.4074 (0.9); 7.4036 (0.6); 7.3923 (0.7); 7.2983 (1.2); 7.2963 (1.2); 7.2882 (1.3); 7.2861 (1.3); 7.2821 (1.1); 7.0850 (1.2); 7.0783 (1.4); 7.0052 (1.3); 6.9981 (1.2); 6.9951 (1.3); 6.9880 (1.1); 6.5474 (1.0); 5.0768 (0.4); 5.0728 (0.5); 5.0692 (0.6); 5.0644 (0.8); 5.0597 (0.6); 5.0560 (0.6); 5.0521 (0.5); 4.3399 (0.7); 4.3325 (0.7); 4.3180 (0.8); 4.3104 (0.8); 3.9075 (1.1); 3.8941 (1.1); 3.8854 (1.0); 3.8721 (1.0); 2.9336 (16.0); 2.8490 (14.1); 2.6633 (11.8); 1.9319 (0.6); −0.0002 (0.9) I-106: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.9425 (2.5); 7.9175 (2.8); 7.8837 (1.0); 7.8690 (1.0); 7.8194 (0.9); 7.8048 (0.9); 7.5284 (0.3); 7.5125 (1.1); 7.4992 (2.4); 7.4462 (2.4); 7.4203 (1.3); 7.3888 (0.4); 7.3766 (1.0); 7.3747 (0.9); 7.3668 (0.7); 7.3617 (1.8); 7.3593 (1.7); 7.3483 (0.8); 7.3441 (1.2); 7.3295 (0.4); 7.3276 (0.4); 7.2753 (0.8); 6.6147 (0.9); 5.2321 (0.4); 5.2251 (0.5); 5.2203 (0.6); 5.2155 (0.4); 5.2086 (0.4); 4.4403 (0.6); 4.4327 (0.6); 4.4182 (0.6); 4.4106 (0.6); 4.0454 (0.7); 4.0319 (0.7); 4.0232 (0.7); 4.0098 (0.6); 2.9171 (16.0); 2.8365 (14.6); 2.6734 (8.2); 2.6673 (1.0); 1.8968 (0.7); −0.0002 (0.9) I-107: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.9528 (2.2); 7.8657 (3.8); 7.5613 (0.4); 7.5458 (1.2); 7.5302 (1.5); 7.5240 (1.5); 7.5083 (0.4); 7.4729 (1.4); 7.4129 (0.6); 7.4096 (0.9); 7.4059 (0.6); 7.3943 (0.7); 7.2837 (0.9); 6.7581 (3.0); 6.5827 (0.9); 4.9035 (0.5); 4.8971 (0.6); 4.8917 (0.9); 4.8863 (0.6); 4.8797 (0.4); 4.2536 (0.8); 4.2460 (0.8); 4.2314 (0.9); 4.2240 (0.8); 3.9114 (1.0); 3.8995 (1.0); 3.8892 (0.9); 3.8774 (0.9); 2.9344 (16.0); 2.8463 (14.0); 2.6601 (11.3); 2.1094 (11.4); 1.9315 (0.6); −0.0002 (1.0) I-108: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.5460 (0.6); 7.5190 (2.1); 7.5101 (1.8); 7.5055 (2.0); 7.4999 (5.2); 7.4967 (4.9); 7.4846 (0.4); 7.4803 (0.4); 7.4611 (0.4); 7.3585 (8.3); 7.2987 (7.9); 7.2754 (2.5); 7.2277 (1.0); 7.2172 (1.6); 7.2101 (1.3); 7.1970 (1.1); 7.1896 (0.7); 6.9996 (2.4); 6.9741 (2.9); 6.9321 (2.9); 6.7551 (1.6); 6.7302 (1.4); 6.1424 (2.0); 5.3361 (1.4); 4.2728 (1.0); 4.2629 (1.3); 4.2378 (1.4); 4.2286 (1.3); 3.9024 (0.5); 3.8861 (0.7); 3.8754 (0.7); 3.8698 (0.8); 3.8629 (0.6); 3.8537 (0.7); 3.8380 (2.6); 3.8171 (0.9); 3.8033 (1.8); 3.7824 (1.2); 3.5514 (2.7); 3.5292 (7.3); 3.5073 (2.9); 3.0120 (0.9); 2.9973 (0.9); 2.9667 (1.4); 2.9512 (1.2); 2.7551 (1.4); 2.7236 (1.3); 2.7099 (1.1); 2.6777 (1.0); 2.3167 (0.3); 2.2903 (16.0); 2.2125 (14.5); 2.1097 (0.5); 2.0959 (0.4); 2.0757 (3.0); 2.0634 (3.2); 2.0536 (8.1); 2.0435 (3.3); 2.0313 (2.9); 2.0110 (0.4); 1.2923 (0.8); 0.0372 (8.8); 0.0262 (0.4) I-109: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.2328 (8.0); 7.3549 (1.6); 7.3286 (3.4); 7.2986 (15.5); 7.0324 (2.0); 7.0240 (2.2); 7.0076 (2.9); 6.9959 (3.7); 6.9823 (3.3); 6.9734 (2.5); 6.9363 (4.7); 6.8715 (1.4); 6.8688 (1.5); 6.8637 (1.8); 6.8611 (1.7); 6.8448 (1.2); 6.8419 (1.2); 6.8370 (1.7); 6.8342 (1.6); 6.8058 (2.4); 6.7996 (3.1); 6.7929 (1.8); 6.7139 (1.6); 6.6893 (1.4); 6.3269 (1.8); 6.2412 (3.1); 6.1822 (2.7); 5.6520 (3.0); 5.6146 (2.8); 5.3374 (5.3); 4.2908 (0.9); 4.2824 (1.4); 4.2566 (1.5); 4.2479 (1.2); 4.1719 (0.5); 4.1481 (0.5); 3.8977 (0.7); 3.8916 (0.8); 3.8824 (0.8); 3.8765 (0.9); 3.8693 (0.8); 3.8569 (2.6); 3.8374 (0.8); 3.8234 (2.0); 3.8026 (1.2); 3.0411 (0.9); 3.0263 (0.9); 2.9965 (1.4); 2.9803 (1.3); 2.7721 (1.2); 2.7411 (1.2); 2.7268 (1.2); 2.6957 (1.0); 2.6796 (1.0); 2.4362 (0.4); 2.3052 (16.0); 2.2278 (15.0); 2.0841 (2.3); 1.9912 (0.4); 1.9745 (0.8); 1.9633 (0.9); 1.9466 (1.6); 1.9299 (1.0); 1.9187 (1.0); 1.9018 (0.6); 1.6416 (0.6); 1.3216 (0.6); 1.2978 (1.1); 1.2741 (0.5); 1.0609 (1.0); 1.0458 (2.5); 1.0391 (2.9); 1.0243 (1.6); 1.0175 (2.9); 1.0108 (2.6); 0.9965 (1.4); 0.9739 (0.4); 0.7742 (1.3); 0.7592 (3.2); 0.7530 (3.0); 0.7428 (2.9); 0.7370 (3.4); 0.7209 (1.2); 0.0491 (0.4); 0.0382 (18.8); 0.0274 (0.9) I-110: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9707 (7.8); 7.2989 (14.6); 7.1322 (0.8); 7.1284 (0.8); 7.1055 (2.0); 7.1019 (2.0); 7.0789 (1.4); 7.0757 (1.6); 7.0300 (2.8); 7.0202 (1.7); 7.0038 (3.6); 6.9754 (0.9); 6.9698 (0.8); 6.9100 (2.9); 6.8525 (1.0); 6.8473 (1.0); 6.8262 (1.7); 6.8044 (0.9); 6.7994 (0.8); 6.7105 (1.6); 6.6864 (1.4); 6.2729 (1.9); 4.2946 (1.0); 4.2859 (1.4); 4.2601 (1.5); 4.2513 (1.3); 4.1712 (0.4); 4.1474 (0.4); 3.9054 (0.8); 3.8898 (0.8); 3.8744 (0.9); 3.8652 (2.8); 3.8447 (0.8); 3.8309 (1.9); 3.8102 (1.2); 3.0455 (0.9); 3.0300 (1.0); 3.0135 (1.8); 3.0011 (1.6); 2.9881 (5.9); 2.9628 (5.4); 2.9375 (1.8); 2.7975 (1.3); 2.7671 (1.2); 2.7524 (1.1); 2.7216 (1.0); 2.3126 (16.0); 2.1812 (15.0); 2.1495 (0.8); 2.1382 (0.8); 2.1213 (1.4); 2.1038 (0.9); 2.0933 (0.8); 2.0845 (2.2); 2.0764 (0.4); 1.6160 (1.6); 1.3936 (6.1); 1.3684 (12.8); 1.3430 (5.9); 1.3213 (0.7); 1.2974 (1.6); 1.2910 (1.5); 1.2737 (0.7); 1.0909 (1.0); 1.0777 (1.9); 1.0710 (2.5); 1.0662 (1.6); 1.0627 (1.5); 1.0581 (1.5); 1.0488 (2.0); 1.0427 (2.3); 1.0299 (1.2); 0.8858 (0.3); 0.8682 (0.3); 0.8326 (1.2); 0.8262 (1.2); 0.8170 (2.6); 0.8096 (2.4); 0.8013 (2.7); 0.7941 (1.7); 0.7841 (0.9); 0.1074 (7.4); 0.0478 (0.6); 0.0370 (17.2); 0.0261 (0.7) I-111: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9690 (7.4); 7.3430 (1.6); 7.3167 (3.5); 7.2989 (15.7); 7.2907 (2.4); 7.0046 (4.3); 6.9792 (4.6); 6.9317 (3.1); 6.8589 (1.5); 6.8537 (1.7); 6.8321 (1.2); 6.8270 (1.7); 6.7986 (2.4); 6.7926 (3.1); 6.7859 (1.8); 6.7142 (1.7); 6.6902 (1.4); 6.3377 (1.8); 4.2747 (1.0); 4.2663 (1.4); 4.2407 (1.5); 4.2320 (1.2); 4.1952 (0.5); 4.1713 (1.4); 4.1475 (1.4); 4.1238 (0.6); 3.8807 (0.8); 3.8646 (0.9); 3.8581 (0.8); 3.8437 (2.8); 3.8238 (0.8); 3.8100 (2.0); 3.7892 (1.2); 3.0316 (1.0); 3.0105 (1.9); 2.9851 (6.1); 2.9708 (1.6); 2.9596 (5.2); 2.9343 (1.8); 2.7647 (1.2); 2.7340 (1.3); 2.7193 (1.2); 2.6885 (1.0); 2.6788 (1.1); 2.4322 (0.4); 2.3373 (0.4); 2.3260 (0.6); 2.3013 (16.0); 2.2281 (14.9); 2.1814 (0.4); 2.0846 (6.9); 1.9851 (0.4); 1.9682 (0.8); 1.9569 (0.9); 1.9403 (1.6); 1.9235 (1.0); 1.9122 (0.9); 1.8957 (0.5); 1.6343 (2.0); 1.3890 (5.7); 1.3637 (11.9); 1.3383 (5.4); 1.3215 (1.8); 1.2977 (3.5); 1.2738 (1.7); 1.0545 (1.0); 1.0393 (2.6); 1.0327 (2.9); 1.0179 (1.6); 1.0110 (2.9); 1.0046 (2.6); 0.9901 (1.4); 0.9731 (0.5); 0.9675 (0.4); 0.7704 (1.4); 0.7553 (3.3); 0.7492 (3.0); 0.7390 (2.9); 0.7331 (3.4); 0.7171 (1.1); 0.1072 (0.6); 0.0480 (0.6); 0.0372 (18.4); 0.0263 (0.9) I-112: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.4109 (8.4); 7.2988 (15.2); 7.1415 (0.8); 7.1377 (0.8); 7.1149 (1.9); 7.1113 (2.0); 7.0883 (1.4); 7.0850 (1.6); 7.0367 (3.3); 7.0102 (4.6); 6.9877 (0.9); 6.9821 (0.8); 6.9140 (2.9); 6.8618 (1.0); 6.8563 (1.1); 6.8353 (1.7); 6.8136 (0.9); 6.8085 (0.8); 6.7188 (1.6); 6.6936 (1.3); 6.1933 (1.9); 5.5710 (3.6); 5.5631 (3.7); 4.4338 (3.2); 4.4259 (3.2); 4.3053 (0.8); 4.2963 (1.4); 4.2710 (1.6); 4.2628 (1.1); 4.0330 (1.5); 4.0097 (4.7); 3.9863 (4.7); 3.9632 (1.5); 3.9330 (0.5); 3.9155 (0.8); 3.8995 (0.8); 3.8855 (2.5); 3.8659 (0.6); 3.8518 (2.0); 3.8313 (1.1); 3.0509 (0.8); 3.0346 (0.8); 3.0058 (1.4); 2.9892 (1.3); 2.8108 (1.1); 2.7798 (1.1); 2.7654 (1.1); 2.7346 (0.9); 2.3397 (0.4); 2.3162 (16.0); 2.2957 (0.6); 2.1850 (14.9); 2.1665 (0.5); 2.1486 (0.7); 2.1376 (0.8); 2.1202 (1.4); 2.1033 (0.9); 2.0919 (0.8); 2.0844 (0.4); 2.0748 (0.4); 1.5989 (14.1); 1.4881 (5.2); 1.4649 (11.1); 1.4416 (5.1); 1.4096 (0.5); 1.3838 (0.4); 1.3608 (0.7); 1.3336 (0.5); 1.3075 (0.4); 1.0933 (0.9); 1.0799 (1.8); 1.0733 (2.4); 1.0688 (1.5); 1.0653 (1.4); 1.0603 (1.5); 1.0513 (2.0); 1.0450 (2.3); 1.0319 (1.2); 0.9850 (0.9); 0.9609 (1.6); 0.9366 (0.7); 0.8337 (1.2); 0.8267 (1.1); 0.8176 (2.5); 0.8103 (2.3); 0.8022 (2.6); 0.7949 (1.6); 0.7845 (0.9); 0.1082 (0.5); 0.0489 (0.5); 0.0381 (18.6); 0.0271 (0.7) I-113: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.0980 (8.5); 7.4563 (1.0); 7.4535 (1.0); 7.4405 (1.8); 7.4273 (1.0); 7.4246 (0.9); 7.2591 (8.8); 7.1851 (1.1); 7.1834 (1.1); 7.1690 (2.2); 7.1675 (2.2); 7.1531 (1.2); 7.1515 (1.2); 7.0769 (1.2); 7.0739 (1.2); 7.0601 (1.7); 7.0466 (0.9); 7.0435 (0.8); 6.9590 (2.7); 6.9438 (2.9); 6.8505 (3.1); 6.8326 (1.6); 6.8196 (1.6); 6.7972 (1.5); 6.6448 (1.7); 6.6298 (1.4); 6.1193 (1.9); 5.8860 (2.7); 5.8848 (2.7); 5.8506 (2.5); 5.8493 (2.4); 5.4687 (2.7); 5.4678 (2.6); 5.4463 (2.5); 5.4452 (2.5); 4.2751 (1.4); 4.2690 (1.4); 4.2537 (1.5); 4.2474 (1.4); 3.8901 (0.3); 3.8778 (0.7); 3.8735 (0.8); 3.8701 (0.9); 3.8674 (0.9); 3.8639 (0.8); 3.8603 (0.9); 3.8576 (0.9); 3.8543 (0.8); 3.8512 (0.7); 3.8480 (0.7); 3.8442 (0.5); 3.8378 (0.4); 3.8136 (2.3); 3.8011 (1.5); 3.7921 (1.9); 3.7795 (1.4); 2.9984 (1.2); 2.9885 (1.2); 2.9711 (1.4); 2.9612 (1.3); 2.7187 (1.5); 2.6991 (1.5); 2.6915 (1.3); 2.6718 (1.2); 2.2619 (16.0); 2.1331 (0.5); 2.1129 (15.0); 1.5587 (3.1); 0.0061 (0.6); −0.0002 (8.5); −0.0067 (0.4) I-114: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.9145 (5.4); 7.5379 (0.8); 7.5223 (4.5); 7.5096 (6.6); 7.4865 (3.0); 7.3952 (3.2); 7.3860 (1.8); 7.3799 (3.0); 7.2938 (1.2); 7.2925 (1.2); 7.2781 (2.1); 7.2633 (1.5); 7.2609 (1.5); 7.2582 (1.6); 7.2371 (1.7); 7.2221 (2.3); 7.2075 (1.0); 6.7082 (4.5); 6.5376 (2.0); 6.5349 (2.0); 4.9913 (0.9); 4.9847 (1.5); 4.9800 (1.6); 4.9752 (1.5); 4.9685 (0.8); 4.3520 (1.3); 4.3446 (1.3); 4.3299 (1.7); 4.3225 (1.6); 4.2144 (1.7); 4.2033 (1.6); 4.1923 (1.3); 4.1813 (1.2); 2.7219 (0.3); 2.6557 (16.0); 1.9701 (1.7); 1.6965 (0.4); −0.0002 (1.0) I-115: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.9253 (5.4); 7.5498 (0.5); 7.5344 (1.6); 7.5191 (3.0); 7.5157 (2.4); 7.4999 (0.6); 7.4683 (2.0); 7.4111 (1.0); 7.4074 (1.4); 7.4035 (0.9); 7.3926 (1.0); 7.2649 (1.0); 7.1959 (2.4); 7.1857 (2.4); 6.8454 (2.7); 6.8353 (2.5); 6.3374 (1.5); 5.1064 (0.8); 5.1039 (0.9); 5.0983 (0.9); 5.0956 (0.9); 5.0913 (0.9); 5.0886 (0.9); 5.0831 (0.8); 5.0806 (0.7); 4.3492 (1.0); 4.3475 (1.0); 4.3411 (1.0); 4.3393 (0.9); 4.3271 (1.0); 4.3254 (1.0); 4.3190 (1.0); 4.3173 (0.9); 3.7962 (1.5); 3.7809 (1.6); 3.7741 (1.4); 3.7588 (1.4); 2.6671 (16.0); 2.2617 (15.2); 1.9859 (1.2); 1.7375 (0.6); −0.0002 (0.9) I-116: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.9413 (5.1); 7.5600 (0.5); 7.5445 (1.7); 7.5290 (3.4); 7.5112 (0.6); 7.4652 (2.4); 7.4106 (1.4); 7.3959 (1.1); 7.2614 (3.3); 6.8922 (3.2); 6.8609 (2.7); 6.3099 (1.6); 5.0027 (0.7); 4.9999 (0.8); 4.9950 (0.8); 4.9905 (1.1); 4.9860 (0.8); 4.9811 (0.8); 4.9783 (0.7); 4.3637 (1.1); 4.3559 (1.1); 4.3417 (1.2); 4.3338 (1.2); 3.8607 (1.4); 3.8466 (1.4); 3.8387 (1.4); 3.8245 (1.3); 2.6793 (16.0); 2.4379 (0.3); 2.2698 (0.8); 2.2071 (11.7); 1.6064 (1.7); −0.0002 (3.2) I-117: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.2689 (15.3); 8.0219 (1.4); 7.6190 (1.0); 7.6081 (9.3); 7.6048 (9.8); 7.5973 (4.2); 7.5927 (4.5); 7.5869 (5.3); 7.5560 (1.1); 7.5376 (1.2); 7.5140 (0.5); 7.4890 (0.8); 7.4378 (0.6); 7.3955 (0.4); 7.3889 (0.6); 7.3814 (0.6); 7.3551 (2.8); 7.2989 (6.2); 7.2631 (1.7); 7.0214 (2.2); 6.9969 (2.4); 6.9049 (3.3); 6.7155 (1.1); 3.7959 (1.2); 3.7818 (1.6); 3.7658 (2.4); 3.7508 (2.8); 3.7358 (2.5); 3.7212 (1.6); 3.7052 (0.9); 3.6402 (1.0); 3.6014 (1.0); 2.9536 (1.0); 2.7554 (0.6); 2.3015 (16.0); 2.1892 (10.8); 2.1026 (1.3); 2.0920 (1.3); 2.0814 (1.8); 2.0615 (1.4); 2.0521 (1.4); 2.0361 (10.1); 1.7319 (1.1); 1.7028 (1.0); 1.2969 (0.8); 0.1139 (0.5); 0.0403 (5.2) I-118: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.2465 (12.0); 7.3503 (2.8); 7.3241 (6.0); 7.2984 (5.1); 7.0304 (5.6); 7.0048 (5.2); 6.9720 (0.4); 6.9245 (3.6); 6.8518 (2.0); 6.8249 (1.9); 6.7923 (3.6); 6.7306 (1.1); 3.7671 (1.0); 3.7374 (2.0); 3.7217 (2.3); 3.7075 (2.2); 3.6774 (0.9); 3.5985 (0.8); 3.5709 (0.9); 2.9204 (1.1); 2.8540 (0.4); 2.7985 (0.5); 2.3506 (0.8); 2.3128 (16.0); 2.2367 (14.2); 2.0653 (1.0); 2.0528 (1.0); 2.0227 (1.3); 2.0103 (1.2); 1.9922 (1.1); 1.9750 (1.5); 1.9637 (1.6); 1.9471 (2.9); 1.9303 (1.7); 1.9192 (1.7); 1.9023 (0.9); 1.7057 (1.0); 1.6915 (0.9); 1.6765 (0.9); 1.3075 (0.4); 1.0646 (1.6); 1.0491 (4.5); 1.0427 (5.1); 1.0279 (2.8); 1.0210 (5.1); 1.0145 (4.7); 1.0001 (2.3); 0.9772 (0.4); 0.7760 (2.2); 0.7608 (5.9); 0.7548 (5.4); 0.7445 (5.3); 0.7386 (6.0); 0.7226 (1.9); 0.0507 (1.7) I-119: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.9139 (5.2); 7.2598 (4.9); 7.0773 (2.2); 7.0621 (3.3); 7.0467 (2.3); 6.9816 (4.2); 6.9680 (4.8); 6.9432 (1.6); 6.8707 (4.7); 6.8076 (2.1); 6.7940 (2.8); 6.7808 (1.4); 6.6682 (2.9); 6.6538 (2.3); 6.2125 (3.3); 5.2968 (0.6); 4.2334 (2.3); 4.2138 (2.2); 3.8583 (2.3); 3.8125 (2.4); 3.8000 (1.9); 3.7917 (2.0); 3.7794 (1.3); 2.9869 (2.0); 2.9778 (2.0); 2.9601 (2.2); 2.9514 (1.9); 2.9011 (0.4); 2.7465 (2.4); 2.7271 (2.6); 2.7005 (2.0); 2.6267 (16.0); 2.4974 (0.4); 2.4801 (0.4); 2.4652 (0.4); 2.3939 (0.6); 2.2711 (15.8); 2.1440 (15.4); 2.0762 (2.1); 1.5793 (6.6); 1.0243 (4.5); 0.7720 (5.0); −0.0002 (5.5) I-120: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.7215 (5.8); 7.2989 (7.9); 7.1815 (0.5); 7.1775 (0.5); 7.1548 (1.2); 7.1509 (1.3); 7.1282 (0.8); 7.1245 (0.9); 7.0419 (0.8); 7.0363 (1.0); 7.0279 (1.7); 7.0180 (1.0); 7.0131 (1.3); 7.0024 (2.0); 6.9914 (0.7); 6.9860 (0.6); 6.9143 (1.9); 6.8816 (1.1); 6.8597 (0.6); 6.8549 (0.5); 6.7148 (1.0); 6.6909 (0.9); 6.0572 (1.2); 4.3216 (0.6); 4.3131 (0.9); 4.2871 (1.0); 4.2790 (0.7); 3.9234 (0.4); 3.9177 (0.5); 3.9087 (0.4); 3.9022 (0.5); 3.8940 (0.5); 3.8854 (1.6); 3.8655 (0.4); 3.8515 (1.3); 3.8310 (0.7); 3.0612 (0.5); 3.0460 (0.5); 3.0166 (1.0); 3.0002 (0.8); 2.8624 (0.4); 2.8047 (16.0); 2.7678 (0.8); 2.7538 (0.8); 2.7226 (0.6); 2.3409 (0.3); 2.3148 (10.1); 2.1830 (9.5); 2.1605 (0.6); 2.1434 (0.9); 2.1262 (0.5); 2.1152 (0.5); 1.6014 (6.7); 1.3039 (1.4); 1.2977 (1.3); 1.1228 (0.6); 1.1095 (1.2); 1.1027 (1.6); 1.0981 (1.0); 1.0949 (1.0); 1.0894 (1.0); 1.0806 (1.3); 1.0744 (1.5); 1.0611 (0.8); 0.9412 (0.5); 0.9195 (1.5); 0.8961 (0.6); 0.8572 (0.8); 0.8499 (0.7); 0.8408 (1.6); 0.8337 (1.4); 0.8258 (1.6); 0.8188 (1.1); 0.8078 (0.5); 0.1079 (0.4); 0.0375 (9.3); 0.0266 (0.4) I-121: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.7079 (3.7); 7.4030 (0.7); 7.3767 (1.5); 7.3503 (0.9); 7.2988 (3.9); 7.0732 (0.8); 7.0471 (0.7); 7.0047 (1.1); 6.9792 (1.2); 6.9296 (1.2); 6.9079 (0.6); 6.9050 (0.6); 6.9000 (0.7); 6.8972 (0.7); 6.8811 (0.5); 6.8782 (0.5); 6.8731 (0.7); 6.8704 (0.6); 6.8277 (0.9); 6.8214 (1.3); 6.8147 (0.8); 6.7020 (0.7); 6.6784 (0.6); 6.1351 (0.8); 4.3083 (0.4); 4.3000 (0.6); 4.2739 (0.7); 4.2657 (0.5); 4.1931 (1.1); 4.1692 (3.5); 4.1454 (3.5); 4.1217 (1.2); 3.8985 (0.3); 3.8831 (0.4); 3.8753 (0.4); 3.8655 (1.1); 3.8317 (0.8); 3.8110 (0.5); 3.0534 (0.4); 3.0385 (0.4); 3.0084 (0.6); 2.9926 (0.6); 2.7924 (10.3); 2.7727 (0.6); 2.7410 (0.5); 2.7267 (0.5); 2.6956 (0.4); 2.3054 (6.7); 2.2193 (6.3); 2.0815 (16.0); 1.9849 (0.4); 1.9682 (0.6); 1.9515 (0.4); 1.9402 (0.4); 1.6240 (3.3); 1.3194 (4.3); 1.2956 (8.7); 1.2718 (4.1); 1.0868 (0.4); 1.0715 (1.1); 1.0648 (1.2); 1.0593 (0.7); 1.0499 (0.6); 1.0431 (1.2); 1.0367 (1.1); 1.0221 (0.5); 0.9179 (0.4); 0.7915 (0.5); 0.7763 (1.4); 0.7701 (1.2); 0.7599 (1.2); 0.7541 (1.4); 0.7379 (0.4); 0.0360 (4.4) I-122: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1520 (6.4); 7.2987 (14.0); 7.1576 (0.8); 7.1536 (0.8); 7.1306 (1.9); 7.1272 (2.1); 7.1007 (1.5); 7.0291 (3.2); 7.0225 (1.7); 7.0040 (4.2); 6.9769 (0.9); 6.9719 (0.9); 6.9118 (3.0); 6.8820 (1.1); 6.8770 (1.1); 6.8553 (1.8); 6.8338 (0.9); 6.8286 (0.9); 6.7128 (1.6); 6.6875 (1.4); 6.2374 (1.5); 5.1212 (0.4); 5.0988 (1.3); 5.0767 (1.3); 5.0553 (0.5); 4.3102 (1.0); 4.3011 (1.3); 4.2758 (1.5); 4.2667 (1.3); 4.1711 (0.6); 4.1474 (0.6); 3.9149 (0.8); 3.8985 (0.8); 3.8731 (2.6); 3.8530 (0.8); 3.8389 (1.8); 3.8182 (1.1); 3.6124 (0.5); 3.0556 (0.9); 3.0400 (0.9); 3.0108 (1.4); 2.9941 (1.3); 2.7974 (1.1); 2.7672 (1.1); 2.7528 (1.0); 2.7215 (0.9); 2.3463 (0.5); 2.3150 (16.0); 2.1803 (14.0); 2.1630 (1.0); 2.1511 (0.9); 2.1343 (1.4); 2.1173 (0.9); 2.1061 (0.9); 2.0833 (3.1); 1.6582 (0.6); 1.6354 (0.6); 1.6067 (6.8); 1.6009 (5.8); 1.5847 (6.7); 1.5790 (5.6); 1.3209 (0.8); 1.2971 (1.6); 1.2733 (0.7); 1.1074 (0.9); 1.0938 (1.8); 1.0874 (2.4); 1.0822 (1.5); 1.0796 (1.5); 1.0745 (1.5); 1.0654 (2.0); 1.0592 (2.4); 1.0461 (1.3); 1.0204 (0.4); 0.8452 (1.1); 0.8384 (1.1); 0.8294 (2.5); 0.8222 (2.4); 0.8135 (2.7); 0.8066 (1.7); 0.7962 (1.0); 0.1080 (1.3); 0.0484 (0.6); 0.0376 (17.8); 0.0268 (0.7) I-123: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1333 (16.0); 7.3876 (3.0); 7.3612 (6.8); 7.3553 (7.2); 7.3482 (7.0); 7.3349 (3.9); 7.2989 (18.2); 7.1396 (5.4); 7.1225 (0.8); 7.1123 (6.8); 7.0614 (3.5); 7.0354 (3.0); 6.9187 (4.2); 6.9116 (4.2); 6.8915 (3.4); 6.8844 (3.4); 6.8745 (2.4); 6.8716 (2.6); 6.8665 (3.0); 6.8637 (3.0); 6.8477 (1.9); 6.8448 (2.1); 6.8397 (2.9); 6.8368 (2.8); 6.8103 (4.0); 6.8041 (5.2); 6.7972 (3.1); 6.2560 (2.7); 6.2497 (2.7); 5.3375 (1.7); 4.1952 (2.2); 4.1852 (2.6); 4.1595 (3.0); 4.1495 (3.3); 4.0404 (0.4); 4.0300 (0.6); 4.0242 (0.9); 4.0136 (1.4); 3.9970 (1.5); 3.9843 (1.7); 3.9749 (1.1); 3.9675 (1.1); 3.9581 (0.8); 3.9462 (4.0); 3.9303 (2.1); 3.9106 (2.8); 3.8945 (2.0); 3.1891 (2.0); 3.1726 (2.0); 3.1443 (3.1); 3.1274 (2.8); 2.9761 (3.0); 2.9463 (2.8); 2.9312 (2.1); 2.9012 (2.0); 2.6931 (0.8); 2.0054 (0.6); 1.9886 (1.3); 1.9775 (1.4); 1.9721 (1.0); 1.9607 (2.8); 1.9440 (1.6); 1.9327 (1.6); 1.9159 (0.8); 1.6015 (9.7); 1.3665 (0.4); 1.3439 (0.9); 1.3036 (5.6); 1.0802 (1.8); 1.0649 (4.4); 1.0583 (5.0); 1.0527 (2.8); 1.0434 (2.8); 1.0365 (5.0); 1.0302 (4.5); 1.0154 (2.4); 0.9931 (0.4); 0.9651 (0.4); 0.9410 (2.0); 0.9192 (6.5); 0.8959 (2.4); 0.7815 (2.3); 0.7662 (5.8); 0.7601 (5.1); 0.7498 (5.0); 0.7442 (6.0); 0.7279 (1.9); 0.1076 (0.8); 0.0483 (0.7); 0.0374 (23.1); 0.0265 (0.9) I-124: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.2941 (5.2); 7.2988 (12.0); 7.1462 (0.9); 7.1198 (2.0); 7.0933 (1.5); 7.0334 (2.8); 7.0245 (1.5); 7.0179 (1.1); 7.0078 (3.7); 6.9800 (0.7); 6.9739 (0.9); 6.9137 (3.1); 6.8768 (1.0); 6.8719 (1.0); 6.8504 (1.8); 6.8285 (0.9); 6.7192 (1.4); 6.6936 (1.2); 6.2021 (1.7); 5.9711 (0.6); 5.9664 (0.8); 5.9493 (0.7); 5.9448 (0.8); 5.8129 (0.7); 5.8082 (0.8); 5.7911 (0.7); 5.7865 (0.8); 4.3115 (1.0); 4.3028 (1.4); 4.2774 (1.5); 4.2686 (1.2); 3.9238 (0.7); 3.9182 (0.8); 3.9030 (0.8); 3.8957 (0.8); 3.8815 (2.8); 3.8619 (0.7); 3.8478 (1.9); 3.8273 (1.1); 3.0557 (0.8); 3.0409 (0.8); 3.0115 (1.3); 2.9950 (1.2); 2.8049 (1.0); 2.7774 (0.9); 2.7636 (0.8); 2.7324 (0.7); 2.7272 (0.6); 2.3405 (0.5); 2.3172 (16.0); 2.1830 (14.9); 2.1570 (0.8); 2.1453 (0.8); 2.1288 (1.4); 2.1117 (0.9); 2.1006 (0.8); 2.0832 (0.4); 1.8271 (2.9); 1.8169 (2.6); 1.8054 (3.1); 1.7952 (2.6); 1.7460 (3.0); 1.7358 (2.7); 1.7243 (3.0); 1.7141 (2.5); 1.5931 (6.1); 1.3463 (0.4); 1.3062 (2.2); 1.1031 (0.9); 1.0886 (1.9); 1.0831 (2.5); 1.0783 (1.6); 1.0700 (1.6); 1.0611 (2.1); 1.0548 (2.4); 1.0418 (1.3); 0.9431 (0.8); 0.9213 (2.2); 0.8978 (0.9); 0.8414 (1.2); 0.8255 (2.7); 0.8185 (2.5); 0.8101 (2.8); 0.8030 (1.8); 0.7926 (1.0); 0.1093 (0.9); 0.0499 (0.6); 0.0392 (14.8); 0.0284 (0.7) I-125: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.2886 (5.6); 8.2800 (1.7); 7.3647 (1.2); 7.3384 (2.7); 7.3299 (1.0); 7.3099 (2.5); 7.3003 (7.9); 7.2983 (8.8); 7.2901 (2.9); 7.0332 (2.2); 7.0088 (4.3); 6.9835 (3.1); 6.9323 (3.4); 6.8694 (1.9); 6.8427 (1.7); 6.8031 (3.3); 6.7164 (1.7); 6.6914 (1.5); 6.2739 (2.4); 5.9688 (0.8); 5.9473 (0.8); 5.9256 (0.4); 5.8103 (0.8); 5.7888 (0.8); 5.7684 (0.3); 4.2968 (1.2); 4.2882 (1.7); 4.2632 (1.8); 4.2541 (1.6); 3.8966 (1.1); 3.8815 (1.3); 3.8620 (3.0); 3.8426 (1.1); 3.8283 (1.9); 3.8195 (0.8); 3.8080 (1.1); 3.0440 (0.9); 3.0316 (1.0); 3.0006 (1.4); 2.9856 (1.4); 2.7746 (1.1); 2.7437 (1.2); 2.7317 (1.2); 2.6984 (0.9); 2.3381 (0.6); 2.3073 (16.0); 2.2262 (14.8); 2.1841 (0.4); 1.9979 (0.4); 1.9805 (0.8); 1.9700 (1.0); 1.9629 (0.9); 1.9529 (1.6); 1.9430 (1.1); 1.9358 (1.2); 1.9255 (1.1); 1.9079 (0.6); 1.8204 (2.8); 1.8107 (3.4); 1.7989 (3.2); 1.7899 (3.3); 1.7806 (1.2); 1.7393 (2.8); 1.7296 (3.4); 1.7178 (3.2); 1.7088 (3.2); 1.6995 (1.2); 1.5957 (7.5); 1.5873 (2.7); 1.3627 (0.4); 1.3021 (2.0); 1.0677 (0.9); 1.0527 (2.9); 1.0454 (3.3); 1.0311 (2.4); 1.0246 (3.3); 1.0176 (3.1); 1.0049 (1.5); 0.9878 (0.6); 0.9705 (0.5); 0.9623 (0.7); 0.9374 (0.9); 0.9214 (1.6); 0.9132 (0.8); 0.8986 (0.7); 0.7784 (1.2); 0.7632 (3.6); 0.7579 (3.7); 0.7484 (3.8); 0.7414 (4.0); 0.7262 (1.3); 0.1092 (0.6); 0.0466 (2.1); 0.0410 (9.5); 0.0391 (10.9); 0.0309 (3.7) I-126: ¹H-NMR(499.9 MHz, CDCl3): δ =7.9136 (5.3); 7.5848 (0.5); 7.5690 (1.7); 7.5563 (4.2); 7.5455 (0.4); 7.5435 (0.4); 7.4563 (2.0); 7.3848 (0.8); 7.3796 (1.4); 7.3753 (1.0); 7.3711 (0.6); 7.3665 (1.0); 7.3621 (0.6); 7.2593 (1.7); 7.1176 (1.9); 7.1023 (2.1); 6.9442 (2.3); 6.8860 (1.3); 6.8708 (1.1); 6.6620 (1.1); 6.6538 (1.1); 4.9467 (0.8); 4.9424 (1.6); 4.9380 (1.5); 4.9336 (1.6); 4.9293 (0.8); 4.7514 (1.7); 4.7277 (2.4); 4.6307 (2.5); 4.6070 (1.7); 4.2059 (1.1); 4.2022 (1.1); 4.1831 (1.2); 4.1794 (1.2); 3.7888 (1.5); 3.7844 (1.6); 3.7660 (1.4); 3.7616 (1.3); 2.6508 (16.0); 2.3075 (0.4); 2.2783 (12.1); 2.2558 (11.3); 1.9877 (0.7); −0.0002 (1.7) I-127: ¹H-NMR(499.9 MHz, CDCl3): δ = 9.1297 (0.3); 8.1906 (16.0); 7.3232 (8.1); 7.3189 (8.1); 7.3097 (7.2); 7.2939 (4.1); 7.2604 (19.5); 7.1093 (6.1); 7.0930 (7.1); 6.9944 (3.7); 6.9829 (4.4); 6.9791 (3.9); 6.9612 (3.7); 6.9477 (3.9); 6.9256 (3.7); 6.8781 (4.1); 6.8739 (4.2); 6.8618 (3.6); 6.8576 (3.7); 6.8441 (2.8); 6.8407 (3.3); 6.8395 (3.2); 6.8294 (2.5); 6.8280 (2.6); 6.8247 (3.2); 6.8234 (3.0); 6.7913 (4.2); 6.7876 (6.0); 6.7836 (3.9); 6.2600 (3.1); 6.2560 (3.2); 6.2016 (6.3); 6.1660 (5.8); 5.6193 (6.3); 5.5971 (6.1); 4.1503 (2.6); 4.1439 (3.1); 4.1283 (3.9); 4.1221 (3.6); 4.1135 (1.0); 4.0992 (0.4); 3.9922 (0.4); 3.9856 (0.7); 3.9822 (1.0); 3.9758 (1.7); 3.9662 (1.8); 3.9582 (2.0); 3.9520 (1.3); 3.9481 (1.2); 3.9418 (0.7); 3.9087 (3.7); 3.8990 (2.8); 3.8869 (3.2); 3.8772 (2.6); 3.1437 (2.4); 3.1335 (2.5); 3.1167 (3.1); 3.1064 (3.1); 2.9380 (3.0); 2.9199 (3.0); 2.9110 (2.6); 2.8928 (2.4); 2.0433 (3.4); 1.9451 (0.7); 1.9349 (1.5); 1.9282 (1.7); 1.9252 (1.2); 1.9181 (3.1); 1.9111 (1.3); 1.9081 (1.8); 1.9014 (1.8); 1.8912 (0.9); 1.5724 (3.2); 1.2727 (0.9); 1.2584 (1.8); 1.2441 (0.9); 1.0129 (2.0); 1.0036 (5.0); 1.0000 (5.6); 0.9963 (3.2); 0.9910 (3.1); 0.9868 (5.5); 0.9832 (5.4); 0.9743 (2.6); 0.9608 (0.4); 0.8817 (0.3); 0.7311 (2.4); 0.7218 (6.3); 0.7186 (5.7); 0.7120 (5.7); 0.7088 (6.8); 0.6992 (2.3); 0.0063 (0.7); −0.0002 (22.9); −0.0066 (1.5) I-128: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.6747 (2.1); 8.6171 (1.6); 8.6089 (1.7); 7.7456 (1.7); 7.2991 (10.6); 7.0350 (3.5); 7.0097 (2.7); 6.9725 (1.6); 6.9676 (1.7); 6.9395 (0.7); 6.7883 (2.3); 6.6029 (1.1); 4.8018 (1.4); 4.2199 (1.2); 4.1939 (1.4); 4.1759 (0.5); 4.0996 (0.6); 3.9909 (0.3); 3.9623 (2.0); 3.9457 (0.6); 3.9351 (1.6); 3.9183 (0.6); 3.0505 (0.5); 3.0340 (0.6); 3.0044 (1.0); 2.9875 (0.9); 2.9215 (0.9); 2.8928 (0.9); 2.8762 (0.5); 2.8462 (0.5); 2.5663 (16.0); 2.5332 (0.5); 2.3702 (0.5); 2.3591 (0.6); 2.3234 (13.9); 2.3194 (13.8); 1.6045 (5.9); 0.1074 (0.6); 0.0483 (0.4); 0.0375 (12.9); 0.0268 (0.6) I-129: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9701 (4.1); 7.3609 (2.5); 7.3535 (2.1); 7.3366 (1.9); 7.3103 (1.2); 7.2984 (6.5); 7.1470 (1.6); 7.1197 (2.0); 7.0199 (1.0); 6.9940 (0.9); 6.9145 (1.3); 6.9073 (1.3); 6.8872 (1.1); 6.8802 (1.7); 6.8725 (1.0); 6.8696 (0.9); 6.8538 (0.6); 6.8506 (0.6); 6.8458 (0.9); 6.8429 (0.8); 6.8234 (1.2); 6.8174 (1.6); 6.8104 (0.8); 6.3166 (0.8); 6.3096 (0.8); 4.1841 (0.6); 4.1739 (0.8); 4.1483 (0.9); 4.1382 (1.0); 4.0086 (0.4); 3.9916 (0.5); 3.9793 (0.5); 3.9626 (0.3); 3.9420 (1.2); 3.9260 (0.6); 3.9063 (0.8); 3.8904 (0.6); 3.1874 (0.6); 3.1708 (0.6); 3.1426 (0.9); 3.1257 (0.8); 3.0214 (0.9); 2.9960 (2.8); 2.9773 (1.1); 2.9707 (3.0); 2.9460 (1.5); 2.9329 (0.7); 2.9030 (0.6); 2.0428 (16.0); 1.9768 (0.4); 1.9660 (0.5); 1.9494 (0.8); 1.9325 (0.5); 1.9213 (0.5); 1.3963 (3.3); 1.3710 (7.0); 1.3456 (3.2); 1.2909 (0.4); 1.0579 (0.6); 1.0429 (1.4); 1.0359 (1.6); 1.0301 (0.8); 1.0211 (0.9); 1.0145 (1.5); 1.0079 (1.4); 0.9932 (0.8); 0.7742 (0.7); 0.7591 (1.8); 0.7533 (1.5); 0.7426 (1.5); 0.7371 (1.8); 0.7207 (0.6); 0.1060 (0.6); 0.0357 (7.8) I-130: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.9135 (5.2); 7.2597 (3.9); 7.0779 (1.0); 7.0622 (2.2); 7.0465 (1.5); 6.9825 (2.6); 6.9675 (3.2); 6.9584 (2.2); 6.9438 (1.1); 6.8703 (3.3); 6.8074 (1.2); 6.7938 (1.9); 6.7801 (1.1); 6.6686 (1.9); 6.6537 (1.7); 6.2127 (2.3); 4.2361 (1.3); 4.2300 (1.4); 4.2148 (1.5); 4.2087 (1.5); 3.8584 (1.1); 3.8510 (1.2); 3.8126 (1.9); 3.8003 (1.2); 3.7913 (1.6); 3.7790 (1.2); 2.9876 (1.1); 2.9776 (1.2); 2.9604 (1.4); 2.9503 (1.4); 2.7468 (1.4); 2.7279 (1.5); 2.7198 (1.3); 2.7007 (1.2); 2.6263 (16.0); 2.2710 (14.1); 2.1441 (13.7); 2.1031 (0.6); 2.0925 (0.9); 2.0858 (1.0); 2.0758 (1.5); 2.0659 (1.0); 2.0592 (0.9); 2.0487 (0.5); 1.5911 (4.8); 1.0239 (2.6); 1.0176 (2.4); 1.0097 (2.5); 1.0071 (2.5); 0.7824 (1.8); 0.7715 (2.9); 0.7681 (3.0); −0.0002 (4.5) I-131: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9635 (5.2); 7.6147 (2.1); 7.6093 (1.5); 7.6003 (3.3); 7.5973 (3.8); 7.4300 (1.8); 7.3869 (0.8); 7.3740 (2.9); 7.3672 (1.1); 7.3570 (0.8); 7.3486 (2.7); 7.2987 (2.4); 7.0316 (1.9); 6.8036 (1.0); 6.8009 (1.0); 6.7775 (0.9); 6.7749 (0.9); 6.5811 (1.3); 4.9614 (0.7); 4.9544 (0.7); 4.9486 (0.9); 4.9410 (1.4); 4.9334 (0.9); 4.9276 (0.8); 4.9206 (0.7); 4.4547 (1.0); 4.4422 (1.0); 4.4173 (1.2); 4.4047 (1.1); 3.9154 (1.4); 3.8943 (1.3); 3.8778 (1.2); 3.8568 (1.2); 2.6863 (16.0); 2.4418 (11.7); 2.2473 (11.2); 1.6627 (1.4); 1.3028 (0.5); 0.9177 (0.5); 0.0362 (2.5) I-132: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9377 (5.2); 7.6040 (2.6); 7.5866 (3.7); 7.3405 (1.8); 7.2988 (10.9); 7.2658 (0.8); 7.2570 (0.8); 7.2513 (1.2); 7.2448 (1.2); 7.2332 (6.9); 7.2271 (7.3); 7.0920 (1.7); 7.0860 (2.9); 7.0800 (1.4); 5.9166 (1.2); 5.3367 (1.8); 4.2371 (0.8); 4.2250 (0.8); 4.1998 (1.1); 4.1899 (1.1); 4.1701 (1.3); 4.1463 (1.3); 4.1230 (0.9); 4.1014 (1.1); 4.0791 (0.6); 3.9664 (1.1); 3.9465 (1.5); 3.9296 (0.7); 3.9097 (1.4); 3.8695 (0.8); 3.8617 (1.0); 3.8580 (1.0); 3.8500 (1.2); 3.8423 (0.7); 3.8300 (0.5); 2.6726 (16.0); 2.0817 (9.3); 2.0433 (1.3); 1.9121 (0.3); 1.8875 (0.3); 1.6706 (0.4); 1.6470 (0.5); 1.6340 (1.2); 1.6074 (2.6); 1.4561 (0.4); 1.4322 (11.7); 1.4202 (10.8); 1.3812 (0.7); 1.3565 (0.4); 1.3198 (1.9); 1.2960 (4.2); 1.2722 (1.7); 1.2222 (0.4); 1.1985 (0.4); 0.9966 (0.9); 0.9801 (0.4); 0.9722 (1.8); 0.9578 (0.3); 0.9478 (0.8); 0.9172 (0.4); 0.1134 (0.8); 0.1066 (4.1); 0.0476 (0.4); 0.0367 (12.4); 0.0259 (0.6) I-133: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9636 (5.1); 7.6466 (0.3); 7.6208 (1.4); 7.5987 (4.1); 7.5771 (0.4); 7.5151 (1.9); 7.4524 (0.8); 7.4438 (1.3); 7.4365 (0.8); 7.4289 (0.5); 7.4222 (0.8); 7.4142 (0.5); 7.2986 (13.7); 7.2668 (3.2); 7.2605 (1.2); 7.2452 (1.4); 7.2388 (4.6); 7.1113 (4.0); 7.0833 (2.8); 6.1074 (1.1); 6.0984 (1.1); 5.3374 (1.4); 4.1705 (0.5); 4.1467 (0.5); 4.1244 (1.2); 4.1135 (1.1); 4.1017 (0.4); 4.0883 (1.3); 4.0771 (1.4); 3.8777 (1.2); 3.8613 (1.4); 3.8411 (0.9); 3.8245 (1.1); 3.6814 (0.5); 3.6701 (0.7); 3.6589 (0.6); 3.6543 (0.7); 3.6427 (0.5); 2.7870 (0.8); 2.7623 (1.6); 2.7406 (1.8); 2.7040 (16.0); 2.0826 (3.3); 2.0183 (1.1); 1.9930 (2.3); 1.9692 (2.4); 1.9437 (0.9); 1.5976 (5.2); 1.3205 (0.7); 1.2967 (1.6); 1.2730 (0.6); 0.9728 (0.5); 0.1071 (4.2); 0.0481 (0.6); 0.0373 (17.0); 0.0264 (0.8) I-134: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.0243 (5.4); 7.6547 (2.9); 7.6476 (3.2); 7.6166 (1.5); 7.5945 (4.4); 7.5726 (0.4); 7.5272 (2.2); 7.5187 (2.6); 7.4903 (3.8); 7.4651 (0.9); 7.4566 (1.5); 7.4491 (1.0); 7.4306 (2.7); 7.4236 (2.2); 7.4024 (1.2); 7.3952 (1.1); 7.2987 (11.2); 6.7359 (2.3); 5.3373 (2.5); 3.5815 (1.0); 3.5581 (1.1); 3.5528 (1.2); 3.5295 (1.1); 3.5063 (0.4); 3.2517 (1.1); 3.2283 (1.2); 3.2231 (1.1); 3.1997 (1.0); 2.7482 (16.0); 1.5974 (1.0); 1.4621 (11.8); 1.2899 (5.8); 1.2662 (8.2); 1.2429 (3.9); 1.0820 (12.2); 0.9173 (0.4); 0.1073 (1.4); 0.0477 (0.6); 0.0371 (12.4) I-135: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.0279 (0.4); 7.9920 (5.2); 7.5683 (0.7); 7.5504 (3.7); 7.5424 (1.5); 7.5291 (1.8); 7.5029 (0.5); 7.4374 (1.8); 7.3626 (0.8); 7.3555 (1.0); 7.3401 (0.8); 7.3328 (1.1); 7.3243 (0.5); 7.2987 (7.4); 7.2884 (0.5); 7.2584 (0.5); 7.2004 (0.4); 7.1889 (4.0); 7.1815 (1.3); 7.1663 (1.4); 7.1588 (4.5); 7.1474 (0.4); 6.9329 (0.4); 6.9028 (0.4); 6.8448 (1.9); 6.7539 (0.5); 6.7425 (4.5); 6.7350 (1.4); 6.7198 (1.2); 6.7124 (3.9); 6.7009 (0.4); 5.3361 (1.0); 4.5252 (0.5); 4.3210 (1.8); 4.2824 (2.2); 4.1508 (1.7); 4.1180 (3.3); 4.0589 (3.2); 4.0261 (1.7); 3.9603 (2.8); 3.9217 (2.4); 3.8713 (0.7); 3.8644 (0.5); 3.8479 (0.8); 3.8410 (1.5); 3.8243 (0.4); 3.8175 (1.8); 3.7932 (1.8); 3.7695 (1.5); 3.7628 (0.8); 3.7461 (0.5); 3.7392 (0.7); 2.7273 (16.0); 1.2923 (1.5); 1.2614 (4.3); 1.2381 (8.6); 1.2147 (4.0); 0.0371 (7.8); 0.0263 (0.3) I-136: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.7028 (5.8); 7.4227 (1.1); 7.3963 (2.3); 7.3699 (1.5); 7.3589 (2.4); 7.3518 (2.5); 7.2985 (7.1); 7.1665 (2.0); 7.1392 (2.5); 7.0872 (1.2); 7.0612 (1.1); 6.9322 (1.9); 6.9256 (2.2); 6.9190 (1.2); 6.9050 (1.6); 6.8983 (1.8); 6.8922 (1.0); 6.8575 (1.5); 6.8513 (1.9); 6.8444 (1.1); 6.0984 (1.0); 6.0913 (1.0); 4.2064 (0.8); 4.1965 (1.0); 4.1706 (1.2); 4.1611 (1.2); 4.0327 (0.5); 4.0162 (0.6); 4.0037 (0.6); 3.9944 (0.4); 3.9870 (0.4); 3.9723 (1.5); 3.9567 (0.7); 3.9366 (1.0); 3.9210 (0.7); 3.2038 (0.7); 3.1872 (0.7); 3.1590 (1.1); 3.1420 (1.0); 3.0096 (1.1); 2.9802 (1.0); 2.9649 (0.8); 2.9350 (0.7); 2.8021 (16.0); 2.0810 (0.5); 2.0064 (0.5); 1.9951 (0.5); 1.9784 (1.0); 1.9617 (0.6); 1.9504 (0.6); 1.5990 (7.1); 1.3436 (0.4); 1.3194 (0.7); 1.3038 (2.3); 1.2962 (2.1); 1.2721 (0.3); 1.0901 (0.7); 1.0749 (1.6); 1.0681 (1.9); 1.0625 (1.0); 1.0531 (1.0); 1.0464 (1.8); 1.0400 (1.7); 1.0252 (0.9); 0.9597 (0.4); 0.9404 (0.8); 0.9187 (2.6); 0.8954 (1.0); 0.7970 (0.8); 0.7816 (2.2); 0.7756 (1.8); 0.7651 (1.8); 0.7595 (2.2); 0.7432 (0.7); 0.1194 (0.4); 0.1073 (10.1); 0.0952 (0.4); 0.0367 (8.3); 0.0259 (0.3) I-137: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1464 (11.5); 7.3954 (2.6); 7.3691 (6.0); 7.3618 (6.8); 7.3547 (6.7); 7.3428 (3.6); 7.2983 (30.0); 7.1553 (4.8); 7.1281 (6.1); 7.0543 (3.2); 7.0281 (2.8); 6.9471 (0.4); 6.9209 (2.9); 6.9164 (2.8); 6.8958 (4.2); 6.8901 (4.6); 6.8719 (1.9); 6.8688 (1.9); 6.8638 (2.7); 6.8342 (3.8); 6.8282 (5.0); 6.8214 (2.8); 6.2853 (2.5); 5.1330 (0.4); 5.1110 (1.4); 5.0896 (1.8); 5.0726 (1.5); 5.0516 (0.5); 4.2034 (1.9); 4.1936 (2.5); 4.1682 (2.8); 4.1577 (2.9); 4.1467 (1.0); 4.1233 (0.5); 4.1017 (0.4); 4.0509 (0.4); 4.0345 (0.8); 4.0241 (1.4); 4.0077 (1.4); 3.9953 (1.5); 3.9866 (1.0); 3.9784 (1.0); 3.9687 (0.7); 3.9557 (3.3); 3.9396 (1.9); 3.9200 (2.4); 3.9040 (1.7); 3.6352 (1.9); 3.6271 (2.4); 3.6190 (2.1); 3.6107 (2.1); 3.1997 (1.8); 3.1830 (1.8); 3.1548 (2.8); 3.1380 (2.6); 2.9898 (2.5); 2.9601 (2.3); 2.9453 (1.8); 2.9151 (1.6); 2.0824 (4.4); 2.0104 (0.6); 1.9936 (1.2); 1.9825 (1.3); 1.9658 (2.5); 1.9490 (1.5); 1.9377 (1.5); 1.9209 (0.8); 1.6697 (0.4); 1.6478 (0.4); 1.6082 (12.6); 1.6040 (16.0); 1.5865 (10.1); 1.5820 (11.1); 1.3203 (1.1); 1.3143 (0.4); 1.2964 (2.4); 1.2726 (1.0); 1.0757 (1.6); 1.0606 (4.1); 1.0538 (4.7); 1.0388 (2.6); 1.0323 (4.6); 1.0258 (4.3); 1.0110 (2.2); 0.9972 (0.7); 0.9726 (0.7); 0.9604 (0.6); 0.9542 (0.4); 0.9481 (0.4); 0.9295 (0.5); 0.7866 (2.0); 0.7714 (5.3); 0.7658 (4.7); 0.7550 (4.5); 0.7495 (5.7); 0.7331 (1.8); 0.1071 (9.4); 0.0477 (1.2); 0.0369 (38.3); 0.0260 (1.5) I-138: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9565 (5.2); 7.2987 (12.7); 7.1347 (2.4); 7.1194 (0.9); 7.1109 (2.0); 7.0923 (1.9); 7.0850 (2.6); 7.0696 (1.2); 7.0666 (1.2); 7.0198 (1.0); 7.0141 (1.1); 6.9910 (1.4); 6.9693 (0.7); 6.9638 (0.7); 6.9493 (1.5); 6.9238 (1.1); 6.8494 (0.8); 6.8441 (0.8); 6.8233 (1.3); 6.8013 (0.7); 6.7964 (0.6); 6.6059 (1.0); 6.5696 (1.1); 6.5473 (1.2); 6.5109 (1.2); 6.2725 (1.5); 5.6538 (2.0); 5.5952 (1.8); 5.3378 (6.2); 5.2142 (2.0); 5.1778 (1.9); 4.2677 (1.1); 4.2426 (1.3); 4.2340 (0.9); 4.1716 (0.7); 4.1478 (0.7); 3.9336 (0.4); 3.9229 (0.6); 3.9163 (0.7); 3.8862 (2.0); 3.8676 (0.5); 3.8523 (1.4); 3.8325 (0.8); 3.0678 (0.7); 3.0521 (0.6); 3.0227 (1.2); 3.0063 (1.1); 2.8494 (0.9); 2.8182 (0.9); 2.8036 (0.9); 2.7731 (0.7); 2.6697 (16.0); 2.3483 (12.2); 2.1241 (0.5); 2.1128 (0.6); 2.0959 (1.1); 2.0838 (3.6); 2.0680 (0.6); 2.0458 (0.5); 1.5979 (2.8); 1.3213 (1.0); 1.2975 (1.9); 1.2738 (0.8); 1.0724 (0.8); 1.0595 (1.5); 1.0527 (1.9); 1.0444 (1.3); 1.0401 (1.3); 1.0305 (1.5); 1.0244 (1.8); 1.0118 (0.9); 0.8171 (0.9); 0.8117 (1.0); 0.8024 (2.1); 0.7951 (2.0); 0.7864 (2.1); 0.7794 (1.2); 0.7695 (0.7); 0.1074 (3.7); 0.0377 (16.6); 0.0270 (0.8) I-139: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.9215 (5.3); 7.5367 (3.3); 7.5264 (2.9); 7.4475 (1.8); 7.3641 (0.7); 7.3591 (0.8); 7.3535 (1.0); 7.3496 (1.0); 7.3460 (0.6); 7.3409 (0.5); 7.2611 (3.8); 7.2042 (0.4); 7.1972 (4.2); 7.1928 (1.4); 7.1837 (1.3); 7.1792 (4.6); 7.1723 (0.5); 6.7660 (0.4); 6.7591 (4.5); 6.7546 (1.4); 6.7455 (1.3); 6.7410 (4.2); 6.7342 (0.4); 6.5356 (1.1); 5.2961 (1.6); 4.1452 (0.7); 4.1350 (1.3); 4.1312 (1.1); 4.1190 (1.9); 4.1160 (1.8); 4.1125 (1.9); 4.1062 (1.2); 4.0997 (1.0); 4.0925 (0.9); 4.0836 (1.8); 4.0641 (0.9); 4.0588 (0.5); 4.0408 (0.9); 4.0253 (1.1); 4.0117 (0.5); 2.6635 (16.0); −0.0002 (4.8) I-140: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.6825 (1.2); 8.6768 (1.3); 8.6195 (0.9); 8.6144 (1.0); 8.6036 (1.0); 8.5983 (1.0); 7.9766 (3.7); 7.7337 (0.6); 7.7280 (0.8); 7.7204 (0.6); 7.7074 (0.7); 7.7017 (0.8); 7.6997 (0.8); 7.6941 (0.7); 7.3785 (0.8); 7.3760 (0.7); 7.3623 (0.8); 7.3600 (0.8); 7.3521 (0.7); 7.3496 (0.7); 7.3300 (1.5); 7.3242 (1.5); 7.2987 (15.8); 7.2809 (1.3); 7.2549 (1.6); 7.1225 (0.9); 7.1164 (0.8); 7.0967 (0.6); 7.0905 (0.6); 7.0159 (1.4); 7.0086 (1.0); 6.9959 (2.4); 6.9878 (0.9); 6.9804 (1.0); 6.7599 (0.4); 6.7471 (0.5); 6.7388 (0.6); 6.7295 (0.7); 6.7134 (0.4); 6.7061 (0.4); 6.3273 (1.0); 4.3124 (0.4); 4.3038 (0.7); 4.2787 (0.8); 4.2701 (0.5); 4.1943 (0.7); 4.1705 (2.1); 4.1467 (2.1); 4.1234 (1.5); 4.1017 (1.8); 4.0793 (0.9); 3.9767 (0.4); 3.9689 (0.4); 3.9604 (0.4); 3.9468 (1.2); 3.9291 (0.3); 3.9131 (0.9); 3.8943 (0.5); 3.1385 (0.4); 3.1229 (0.4); 3.0931 (0.7); 3.0774 (0.7); 2.9348 (0.6); 2.9029 (0.5); 2.8897 (0.5); 2.8580 (0.4); 2.6726 (11.0); 2.4426 (7.6); 2.0963 (0.6); 2.0829 (16.0); 2.0451 (0.9); 2.0231 (0.3); 2.0119 (0.4); 1.9950 (0.6); 1.9779 (0.4); 1.9669 (0.4); 1.6943 (0.3); 1.6703 (0.8); 1.6615 (0.6); 1.6484 (1.2); 1.6391 (1.0); 1.6269 (0.9); 1.6221 (1.1); 1.5997 (0.6); 1.4562 (0.4); 1.4304 (0.6); 1.4051 (0.6); 1.3809 (0.4); 1.3202 (2.8); 1.2964 (5.6); 1.2726 (2.6); 0.9966 (1.5); 0.9801 (1.4); 0.9720 (3.4); 0.9637 (0.8); 0.9579 (1.2); 0.9537 (1.5); 0.9479 (1.9); 0.9411 (0.7); 0.9357 (0.6); 0.9308 (0.7); 0.9260 (1.0); 0.7187 (0.4); 0.7082 (0.9); 0.7034 (1.3); 0.6975 (1.1); 0.6914 (1.3); 0.6862 (1.2); 0.6807 (1.2); 0.1061 (5.1); 0.0472 (0.6); 0.0364 (18.0); 0.0255 (0.6) I-141: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.2914 (11.6); 7.3869 (3.0); 7.3613 (12.0); 7.3561 (7.7); 7.3343 (3.9); 7.2987 (34.0); 7.1575 (6.4); 7.1303 (7.9); 7.0473 (3.8); 7.0214 (3.4); 6.9474 (0.4); 6.9305 (3.0); 6.9233 (3.0); 6.9172 (2.7); 6.9100 (2.7); 6.9032 (2.8); 6.8958 (5.0); 6.8898 (4.8); 6.8843 (3.6); 6.8684 (2.4); 6.8606 (3.3); 6.8340 (4.8); 6.8279 (6.2); 6.8210 (3.5); 6.2510 (3.2); 6.0024 (0.6); 5.9802 (1.7); 5.9584 (1.7); 5.9366 (0.6); 5.8433 (0.6); 5.8218 (1.8); 5.7999 (1.8); 5.7784 (0.6); 4.2048 (2.5); 4.1948 (3.0); 4.1691 (3.6); 4.1592 (3.8); 4.0541 (0.4); 4.0377 (1.1); 4.0270 (1.7); 4.0106 (1.8); 3.9979 (2.0); 3.9884 (1.3); 3.9813 (1.4); 3.9634 (4.0); 3.9474 (2.0); 3.9278 (2.7); 3.9117 (1.8); 3.2005 (1.8); 3.1842 (1.8); 3.1556 (2.8); 3.1389 (2.6); 2.9965 (2.0); 2.9913 (2.2); 2.9669 (1.9); 2.9618 (2.1); 2.9521 (1.5); 2.9465 (1.6); 2.9217 (1.3); 2.9167 (1.5); 2.8045 (0.8); 2.0065 (0.7); 1.9893 (1.5); 1.9781 (1.7); 1.9613 (3.2); 1.9445 (1.8); 1.9333 (1.8); 1.9166 (0.9); 1.8271 (5.9); 1.8196 (7.0); 1.8053 (6.1); 1.7978 (7.0); 1.7459 (6.2); 1.7385 (7.3); 1.7242 (6.0); 1.7167 (6.8); 1.5968 (16.0); 1.3676 (0.4); 1.3430 (0.9); 1.3039 (5.5); 1.0727 (2.2); 1.0575 (5.2); 1.0508 (6.1); 1.0359 (3.4); 1.0291 (5.8); 1.0227 (5.3); 1.0080 (2.8); 0.9855 (0.6); 0.9595 (0.7); 0.9408 (2.1); 0.9192 (6.4); 0.8960 (2.4); 0.8164 (0.4); 0.7834 (2.7); 0.7681 (6.8); 0.7622 (6.1); 0.7517 (5.8); 0.7460 (7.0); 0.7298 (2.1); 0.1072 (2.1); 0.0480 (1.4); 0.0372 (41.6); 0.0263 (1.7) I-142: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9508 (1.0); 7.9441 (4.6); 7.2985 (6.3); 7.2411 (2.0); 7.1475 (0.7); 7.1442 (0.7); 7.1208 (1.6); 7.1167 (1.9); 7.0882 (3.3); 7.0613 (1.7); 7.0570 (1.8); 7.0411 (1.1); 7.0355 (1.6); 7.0169 (1.1); 7.0123 (1.3); 6.9906 (0.6); 6.9851 (0.6); 6.8657 (0.6); 6.8603 (0.7); 6.8390 (1.2); 6.8173 (0.6); 6.8123 (0.6); 6.2313 (1.2); 5.3347 (1.8); 4.2339 (0.6); 4.2263 (1.1); 4.2013 (1.1); 4.1929 (0.9); 4.1690 (1.1); 4.1452 (1.0); 4.1225 (1.9); 4.1004 (3.3); 4.0780 (1.7); 3.9383 (0.4); 3.9293 (0.5); 3.9198 (0.6); 3.8994 (1.7); 3.8832 (1.0); 3.8736 (0.4); 3.8660 (1.3); 3.8481 (0.8); 3.0627 (0.6); 3.0465 (0.6); 3.0339 (4.6); 3.0179 (1.2); 3.0012 (1.0); 2.8923 (0.8); 2.8617 (0.9); 2.8470 (0.6); 2.8164 (0.6); 2.6723 (14.1); 2.3492 (1.8); 2.3385 (0.9); 2.3238 (10.3); 2.1563 (0.6); 2.1410 (0.5); 2.1294 (0.6); 2.1212 (0.7); 2.1124 (1.0); 2.0948 (1.3); 2.0815 (16.0); 2.0413 (0.6); 1.6936 (0.4); 1.6691 (1.0); 1.6603 (0.4); 1.6470 (1.3); 1.6382 (0.7); 1.6207 (1.1); 1.5982 (0.5); 1.4794 (0.3); 1.4641 (0.4); 1.4549 (0.8); 1.4455 (0.4); 1.4289 (1.1); 1.4036 (1.2); 1.3798 (0.8); 1.3694 (0.4); 1.3558 (0.5); 1.3396 (0.4); 1.3186 (1.7); 1.2947 (4.3); 1.2710 (1.5); 1.2635 (0.4); 1.2397 (0.4); 1.0796 (0.6); 1.0770 (0.6); 1.0655 (1.7); 1.0586 (2.0); 1.0481 (1.1); 1.0445 (1.0); 1.0366 (1.8); 1.0303 (1.9); 1.0164 (0.8); 1.0095 (0.5); 0.9953 (2.8); 0.9789 (1.0); 0.9709 (5.4); 0.9566 (0.8); 0.9465 (2.2); 0.9156 (0.5); 0.8909 (0.5); 0.8678 (0.5); 0.8306 (0.9); 0.8244 (1.0); 0.8151 (1.9); 0.8078 (2.0); 0.7988 (2.0); 0.7912 (1.3); 0.7822 (0.7); 0.1127 (1.0); 0.1062 (2.8); 0.0355 (7.4); 0.0246 (0.3) I-143: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.0094 (5.3); 7.5950 (1.5); 7.5749 (4.2); 7.5723 (3.6); 7.5592 (0.4); 7.5547 (0.4); 7.4835 (2.0); 7.4536 (0.4); 7.4279 (21.0); 7.4067 (1.0); 7.3988 (0.7); 7.2984 (2.4); 6.3373 (1.6); 6.0795 (1.0); 6.0748 (1.3); 5.9068 (0.9); 5.9021 (1.3); 5.8973 (0.9); 5.3335 (2.5); 4.7576 (1.2); 4.7526 (1.2); 4.6921 (1.2); 4.6870 (1.2); 2.7327 (16.0); 2.0729 (0.6); 1.2919 (0.7); 0.1096 (1.1); 0.0362 (3.0) I-144: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.9500 (5.0); 7.5200 (6.9); 7.4341 (4.4); 7.3359 (2.8); 7.2584 (4.2); 6.9615 (0.4); 6.9468 (0.5); 6.9150 (2.7); 6.8972 (6.3); 6.6860 (3.0); 6.6707 (2.7); 6.6113 (0.6); 6.5725 (3.3); 5.2952 (1.8); 4.1339 (6.8); 4.1179 (7.2); 4.0341 (1.7); 4.0153 (2.9); 2.7247 (0.4); 2.6630 (16.0); 2.2822 (1.4); 2.2344 (14.6); 2.1731 (0.8); 2.0322 (14.5); 1.6016 (0.4); 1.2559 (0.6); −0.0002 (4.9) I-145: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.5306 (0.6); 7.5151 (1.6); 7.4996 (1.8); 7.4919 (2.0); 7.4762 (0.7); 7.4076 (2.0); 7.3601 (1.2); 7.3447 (1.0); 7.2592 (4.1); 6.9892 (2.6); 6.9854 (2.4); 6.9750 (2.4); 6.9003 (1.3); 6.8849 (1.0); 4.7171 (1.4); 4.1491 (0.6); 4.1435 (1.1); 4.1281 (1.3); 4.1228 (0.9); 3.9091 (0.4); 3.9032 (0.6); 3.8979 (0.6); 3.8920 (0.7); 3.8858 (0.9); 3.8812 (1.8); 3.8606 (1.3); 3.8503 (0.8); 2.9734 (0.5); 2.9631 (0.6); 2.9459 (1.0); 2.9353 (1.0); 2.8527 (0.8); 2.8349 (0.9); 2.8250 (0.8); 2.8072 (0.7); 2.5795 (14.3); 2.5470 (0.3); 2.3914 (14.2); 2.2747 (16.0); 2.2196 (0.4); 2.2012 (0.4); 1.5881 (0.4); 0.0710 (3.5); −0.0002 (4.8); −0.0066 (0.4) I-146: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.5302 (0.5); 7.5147 (1.4); 7.4991 (1.6); 7.4916 (1.9); 7.4760 (0.6); 7.4079 (1.8); 7.3599 (1.1); 7.3446 (0.9); 7.2591 (2.8); 6.9888 (2.4); 6.9853 (2.3); 6.9748 (2.1); 6.9001 (1.2); 6.8847 (0.9); 4.7263 (1.4); 4.1475 (0.6); 4.1421 (1.0); 4.1266 (1.2); 4.1214 (0.8); 3.9082 (0.4); 3.9022 (0.6); 3.8970 (0.6); 3.8912 (0.7); 3.8805 (1.7); 3.8601 (1.1); 3.8498 (0.7); 2.9728 (0.5); 2.9626 (0.5); 2.9453 (1.0); 2.9348 (0.9); 2.8531 (0.8); 2.8352 (0.8); 2.8253 (0.7); 2.8077 (0.6); 2.5787 (12.1); 2.3909 (12.0); 2.2748 (16.0); 1.5934 (1.1); −0.0002 (3.3) I-147: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1266 (16.0); 7.3610 (6.9); 7.3540 (7.4); 7.2986 (28.3); 7.1781 (6.5); 7.1505 (9.8); 7.1224 (2.9); 7.1187 (3.2); 7.0710 (2.4); 7.0653 (2.9); 7.0470 (2.7); 7.0425 (3.5); 7.0205 (1.6); 7.0150 (1.6); 6.9503 (4.3); 6.9432 (4.2); 6.9231 (3.4); 6.9160 (3.4); 6.9038 (2.1); 6.8984 (2.0); 6.8770 (3.3); 6.8553 (1.7); 6.8499 (1.6); 6.1439 (3.0); 5.3379 (0.6); 4.2090 (2.4); 4.1989 (2.9); 4.1732 (3.4); 4.1632 (3.8); 4.0718 (0.4); 4.0555 (1.0); 4.0451 (1.6); 4.0293 (1.8); 4.0154 (1.8); 4.0068 (1.2); 3.9990 (1.2); 3.9893 (0.8); 3.9789 (4.3); 3.9634 (2.4); 3.9432 (3.0); 3.9276 (2.2); 3.2102 (2.2); 3.1937 (2.2); 3.1654 (3.4); 3.1487 (3.2); 3.0043 (3.3); 2.9744 (3.2); 2.9595 (2.4); 2.9291 (2.2); 2.1590 (0.6); 2.1417 (1.2); 2.1306 (1.4); 2.1136 (2.5); 2.0962 (1.5); 2.0845 (1.7); 2.0677 (0.7); 1.5879 (12.6); 1.2976 (0.8); 1.1100 (1.2); 1.1069 (1.2); 1.0953 (4.1); 1.0891 (4.8); 1.0785 (2.8); 1.0746 (2.2); 1.0670 (4.4); 1.0608 (4.5); 1.0499 (1.7); 1.0469 (1.6); 0.9194 (0.6); 0.8969 (0.5); 0.8420 (2.5); 0.8355 (2.3); 0.8267 (5.1); 0.8192 (5.0); 0.8101 (5.8); 0.8028 (3.3); 0.7932 (1.9); 0.7711 (0.4); 0.0485 (1.2); 0.0375 (35.8); 0.0271 (1.5) I-148: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.6134 (4.6); 8.5969 (3.1); 8.5803 (2.8); 8.3197 (7.6); 8.2906 (0.3); 7.6531 (4.4); 7.6361 (4.6); 7.4188 (2.7); 7.3985 (3.0); 7.3817 (3.0); 7.3716 (1.2); 7.3631 (1.2); 7.3546 (1.6); 7.3486 (1.3); 7.3411 (1.0); 7.3329 (0.8); 7.2983 (6.2); 7.0579 (0.4); 7.0214 (2.4); 6.9959 (2.8); 6.9299 (3.1); 6.7168 (1.7); 6.6923 (1.4); 6.2299 (2.2); 4.3686 (1.2); 4.3583 (1.3); 4.3333 (1.4); 4.3228 (1.5); 4.2424 (0.5); 4.1686 (1.0); 4.1448 (1.0); 4.1213 (0.5); 3.9694 (0.6); 3.9551 (0.8); 3.9368 (0.8); 3.9253 (0.7); 3.9208 (0.7); 3.8874 (2.1); 3.8661 (1.1); 3.8521 (1.7); 3.8307 (1.1); 3.0843 (1.0); 3.0696 (1.0); 3.0388 (1.3); 3.0238 (1.2); 2.7768 (1.4); 2.7436 (1.4); 2.7315 (1.2); 2.6979 (1.0); 2.4409 (16.0); 2.3600 (0.8); 2.3378 (1.0); 2.3159 (15.2); 2.1936 (14.2); 2.1050 (0.9); 2.0807 (5.0): 1.6993 (0.5): 1.3186 (1.1); 1.2948 (2.3); 1.2710 (1.1); 0.9711 (0.4); 0.1075 (0.4); 0.0358 (6.8) I-149: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.7500 (6.2); 8.4871 (4.3); 8.4181 (2.7); 8.4018 (2.8); 7.8519 (2.5); 7.8357 (2.4); 7.6405 (3.2); 7.6232 (3.4); 7.4022 (1.8); 7.3547 (0.7); 7.3459 (0.7); 7.3379 (1.1); 7.3319 (0.9); 7.3243 (0.7); 7.3162 (0.5); 7.2983 (5.5); 7.0230 (1.8); 6.9975 (2.1); 6.9320 (2.1); 6.7300 (1.2); 6.7051 (1.0); 6.1511 (1.5); 4.3642 (0.8); 4.3539 (0.9); 4.3291 (1.0); 4.3187 (1.0); 4.1687 (0.6); 4.1448 (0.6); 4.0491 (16.0); 3.9724 (0.4); 3.9600 (0.5); 3.9392 (0.6); 3.9254 (1.1); 3.9084 (0.3); 3.8959 (1.6); 3.8746 (0.8); 3.8607 (1.3); 3.8395 (0.8); 3.0783 (0.7); 3.0637 (0.7); 3.0330 (1.0); 3.0178 (0.9); 2.7866 (1.0); 2.7538 (1.0); 2.7412 (0.8); 2.7081 (0.7); 2.3399 (0.4); 2.3152 (11.2); 2.1984 (10.4); 2.0808 (3.1); 1.6921 (0.4); 1.3187 (0.7); 1.2949 (1.5); 1.2710 (0.7); 0.1076 (0.4); 0.0360 (6.1) I-150: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.7825 (4.1); 8.7771 (2.6); 8.7676 (2.7); 8.7623 (4.2); 7.4856 (4.4); 7.4802 (2.8); 7.4708 (2.8); 7.4654 (4.3); 7.2985 (11.6); 7.1942 (0.4); 7.1874 (0.5); 7.1671 (1.4); 7.1604 (1.3); 7.1503 (3.5); 7.1390 (1.4); 7.1282 (2.1); 7.1007 (0.7); 7.0879 (1.7); 7.0623 (2.4); 7.0250 (2.3); 6.9585 (1.4); 6.9323 (1.0); 6.8642 (0.8); 6.8577 (0.8); 6.8409 (1.1); 6.8322 (1.1); 6.8215 (0.6); 6.8104 (0.6); 4.8753 (1.6); 4.2537 (0.6); 4.2452 (1.4); 4.2196 (1.3); 4.2110 (0.8); 4.1939 (0.4); 4.1701 (1.0); 4.1463 (1.0); 4.1226 (0.4); 3.9990 (0.4); 3.9889 (0.6); 3.9799 (0.6); 3.9702 (0.8); 3.9544 (1.8); 3.9209 (1.2); 3.9028 (0.7); 3.0597 (0.5); 3.0428 (0.5); 3.0137 (1.1); 2.9960 (1.0); 2.9256 (0.9); 2.8959 (0.9); 2.8793 (0.6); 2.8503 (0.6); 2.5007 (16.0); 2.3340 (11.8); 2.3151 (11.2); 2.1464 (0.6); 2.1356 (0.6); 2.1185 (1.0); 2.1012 (0.7); 2.0822 (4.6); 1.6283 (2.1); 1.3203 (1.2); 1.2965 (2.4); 1.2727 (1.2); 1.0862 (0.6); 1.0714 (1.8); 1.0644 (2.1); 1.0500 (1.0); 1.0427 (1.9); 1.0361 (2.0); 1.0221 (0.7); 0.8338 (0.8); 0.8191 (2.3); 0.8139 (2.3); 0.8019 (2.2); 0.7963 (2.2); 0.7805 (0.6); 0.1073 (0.9); 0.0479 (0.7); 0.0372 (14.0); 0.0263 (0.6) I-151: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.1189 (16.0); 7.6061 (9.8); 7.5959 (8.2); 7.5791 (0.9); 7.3657 (5.3); 7.2964 (7.3); 7.2923 (7.7); 7.2809 (0.7); 7.2726 (2.2); 7.2671 (2.9); 7.2605 (19.7); 7.2497 (2.3); 7.1243 (6.1); 7.1079 (7.4); 6.9526 (4.3); 6.9484 (4.5); 6.9363 (3.7); 6.9321 (3.8); 6.0300 (3.4); 4.1553 (2.8); 4.1491 (3.3); 4.1335 (3.6); 4.1272 (3.9); 4.0208 (0.4); 4.0142 (0.9); 4.0106 (1.1); 4.0042 (1.9); 3.9943 (2.0); 3.9869 (2.1); 3.9808 (1.4); 3.9765 (1.3); 3.9703 (0.7); 3.9265 (3.9); 3.9169 (3.1); 3.9046 (3.3); 3.8951 (2.8); 3.1355 (2.4); 3.1250 (2.5); 3.1084 (3.5); 3.0978 (3.4); 2.9774 (3.4); 2.9593 (3.4); 2.9503 (2.7); 2.9321 (2.5); 2.6072 (0.4); 1.5517 (6.0); 1.2553 (0.8); 0.0060 (0.9); −0.0002 (19.7); −0.0064 (1.5) I-152: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.1188 (16.0); 7.6063 (9.7); 7.5986 (4.9); 7.5960 (7.2); 7.5788 (0.5); 7.3667 (4.9); 7.2965 (7.4); 7.2923 (7.2); 7.2725 (2.6); 7.2670 (3.4); 7.2606 (19.6); 7.2496 (1.5); 7.1243 (5.9); 7.1079 (6.8); 6.9527 (4.4); 6.9485 (4.3); 6.9364 (3.6); 6.9322 (3.4); 6.0339 (3.2); 4.1552 (2.9); 4.1489 (3.1); 4.1334 (3.5); 4.1271 (3.4); 4.0207 (0.6); 4.0143 (1.0); 4.0107 (1.3); 4.0042 (1.9); 3.9944 (1.9); 3.9868 (1.9); 3.9825 (1.1); 3.9806 (1.1); 3.9765 (1.0); 3.9701 (0.5); 3.9265 (3.8); 3.9169 (3.0); 3.9045 (3.1); 3.8950 (2.4); 3.4879 (0.6); 3.1355 (2.4); 3.1249 (2.4); 3.1083 (3.3); 3.0978 (3.0); 2.9775 (3.3); 2.9593 (3.3); 2.9504 (2.5); 2.9322 (2.3); 2.6073 (0.7); 1.5530 (5.2); 1.2553 (0.6); 0.0062 (1.6); −0.0002 (19.8); −0.0067 (0.8) I-153: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1653 (3.3); 8.1409 (3.5); 7.2983 (38.6); 7.2320 (0.6); 7.2158 (0.9); 7.2059 (1.1); 7.1892 (1.2); 7.1786 (1.5); 7.1553 (1.7); 7.1296 (1.0); 7.1048 (0.7); 7.0998 (0.5); 7.0784 (0.3); 7.0140 (1.2); 6.9839 (1.4); 6.9217 (1.1); 6.8903 (1.1); 6.7110 (0.6); 6.6867 (1.0); 6.6651 (0.6); 6.1834 (0.7); 6.1180 (0.7); 4.3248 (0.4); 4.3151 (0.8); 4.3045 (0.6); 4.2908 (0.6); 4.2800 (1.0); 4.2697 (0.5); 3.9084 (0.6); 3.8933 (0.6); 3.8697 (1.7); 3.8469 (0.4); 3.8368 (1.0); 3.8163 (0.5); 3.0525 (0.5); 3.0142 (0.6); 3.0078 (0.7); 2.9995 (0.6); 2.9917 (0.6); 2.9070 (0.6); 2.8940 (0.5); 2.8819 (0.4); 2.8666 (0.6); 2.7792 (0.6); 2.7544 (0.6); 2.7404 (0.6); 2.7094 (0.4); 2.7016 (0.5); 2.3385 (0.4); 2.3086 (10.6); 2.1787 (5.6); 2.1461 (5.6); 2.0392 (0.3); 2.0220 (0.4); 2.0127 (0.4); 2.0000 (0.6); 1.9825 (0.6); 1.9731 (0.8); 1.9557 (0.8); 1.9432 (0.4); 1.9339 (0.4); 1.9168 (0.4); 1.7648 (0.4); 1.7572 (0.4); 1.7518 (0.5); 1.7444 (0.6); 1.7377 (0.4); 1.7296 (0.4); 1.7235 (0.5); 1.7159 (0.5); 1.7026 (0.4); 1.5781 (16.0); 1.2983 (0.9); 0.9416 (0.3); 0.9202 (1.0); 0.8969 (0.4); 0.0487 (1.8); 0.0379 (50.8); 0.0270 (1.9) I-154: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.0367 (4.6); 7.5989 (1.5); 7.5797 (3.8); 7.4870 (1.9); 7.4537 (0.8); 7.4427 (1.4); 7.4319 (3.0); 7.4032 (2.8); 7.2983 (10.6); 6.9827 (3.7); 6.9535 (3.2); 6.5887 (1.0); 4.9199 (0.9); 4.8869 (0.9); 3.9353 (0.5); 3.8517 (16.0); 2.7829 (0.8); 2.7547 (14.0); 2.6993 (0.4); 1.3221 (0.5); 1.2933 (1.1); 0.8898 (0.4); 0.8730 (0.4); 0.1076 (2.6); 0.0480 (0.6); 0.0375 (12.9); 0.0266 (0.6) I-155: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9810 (2.8); 7.9566 (2.8); 7.2986 (19.6); 7.2114 (0.7); 7.1942 (0.6); 7.1862 (2.0); 7.1788 (1.0); 7.1669 (1.3); 7.1586 (0.8); 7.1499 (0.6); 7.1377 (1.6); 7.1293 (0.9); 7.1192 (1.3); 7.1148 (1.3); 7.1066 (0.6); 7.0901 (0.5); 7.0237 (1.2); 6.9982 (1.4); 6.9244 (1.1); 6.8946 (1.1); 6.7220 (0.6); 6.6985 (1.0); 6.6775 (0.5); 6.2293 (0.7); 6.1603 (0.7); 4.2987 (0.5); 4.2905 (0.9); 4.2828 (0.6); 4.2640 (0.6); 4.2558 (1.0); 4.2479 (0.6); 3.9088 (0.5); 3.8935 (0.6); 3.8674 (1.8); 3.8469 (0.5); 3.8346 (1.1); 3.8142 (0.6); 3.0483 (0.4); 3.0408 (0.5); 3.0337 (0.4); 3.0264 (0.4); 3.0042 (0.6); 2.9969 (0.7); 2.9879 (0.6); 2.9803 (0.6); 2.9011 (0.6); 2.8896 (0.4); 2.8740 (0.4); 2.8611 (0.6); 2.7966 (0.7); 2.7708 (0.7); 2.7660 (0.6); 2.7566 (0.6); 2.7515 (0.6); 2.7261 (0.6); 2.7203 (0.5); 2.6709 (16.0); 2.3101 (11.2); 2.1872 (5.6); 2.1560 (5.6); 2.0840 (0.8); 2.0196 (0.3); 2.0022 (0.4); 1.9929 (0.4); 1.9798 (0.7); 1.9758 (0.6); 1.9627 (0.7); 1.9533 (0.8); 1.9362 (0.8); 1.9233 (0.4); 1.9139 (0.4); 1.8967 (0.4); 1.7537 (0.4); 1.7471 (0.4); 1.7403 (0.5); 1.7337 (0.5); 1.7260 (0.4); 1.7193 (0.4); 1.7115 (0.5); 1.7052 (0.5); 1.6986 (0.4); 1.6919 (0.4); 1.5911 (8.7); 1.3217 (0.4); 1.2979 (0.9); 0.9202 (0.6); 0.0488 (0.9); 0.0380 (25.2); 0.0289 (0.7); 0.0272 (0.9) I-156: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.0662 (16.0); 7.6775 (0.3); 7.5574 (0.9); 7.5470 (10.9); 7.5344 (4.9); 7.5187 (1.1); 7.2627 (5.6); 7.2584 (8.8); 7.2297 (2.1); 7.2253 (2.8); 7.2167 (2.6); 7.2122 (3.2); 7.2070 (1.6); 7.2004 (0.3); 7.1965 (0.3); 7.1591 (2.8); 7.1543 (3.8); 7.1472 (5.9); 7.1399 (7.1); 7.1316 (1.7); 7.1226 (2.7); 7.1158 (15.4); 7.1106 (11.3); 7.1070 (5.8); 7.1030 (6.6); 5.8108 (3.9); 3.9784 (0.4); 3.9747 (0.5); 3.9662 (1.2); 3.9568 (1.7); 3.9523 (1.5); 3.9475 (1.8); 3.9383 (1.3); 3.9299 (0.6); 3.9261 (0.5); 3.3707 (2.7); 3.3632 (2.8); 3.3492 (3.1); 3.3417 (3.0); 3.0213 (2.5); 3.0117 (2.6); 2.9946 (3.0); 2.9849 (2.9); 2.9726 (3.5); 2.9599 (3.4); 2.9510 (3.2); 2.9383 (3.1); 2.7010 (3.1); 2.6816 (3.1); 2.6743 (2.9); 2.6549 (2.8); 2.1657 (0.9); 1.9962 (1.6); −0.0002 (6.1); −0.0064 (0.4) I-157: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.5877 (1.1); 7.5682 (2.8); 7.5649 (2.5); 7.4429 (1.4); 7.4139 (0.6); 7.4039 (0.9); 7.3966 (0.7); 7.3832 (0.6); 7.3764 (0.4); 7.2986 (13.5); 7.0347 (2.6); 7.0092 (1.9); 6.9550 (1.1); 6.9288 (0.6); 4.6804 (1.0); 4.2132 (0.8); 4.1872 (0.9); 4.1697 (0.3); 3.9684 (0.5); 3.9452 (1.3); 3.9147 (1.0); 3.8981 (0.4); 3.0411 (0.4); 3.0247 (0.4); 2.9952 (0.7); 2.9789 (0.7); 2.9067 (0.7); 2.8770 (0.6); 2.8608 (0.4); 2.8301 (0.3); 2.5760 (11.7); 2.5600 (0.9); 2.3191 (16.0); 1.5850 (11.2); 1.3042 (0.8); 1.2975 (0.8); 0.9200 (0.8); 0.8963 (0.3); 0.1074 (0.4); 0.0487 (0.8); 0.0379 (15.9); 0.0271 (0.7) I-158: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.9079 (6.3); 8.9070 (6.2); 8.8864 (0.6); 8.5297 (9.5); 8.5072 (0.8); 8.4290 (6.5); 8.4278 (6.5); 8.2951 (0.6); 7.6427 (5.0); 7.6394 (4.6); 7.6308 (2.4); 7.6254 (3.4); 7.5965 (0.4); 7.3836 (2.6); 7.3378 (1.1); 7.3289 (1.2); 7.3243 (0.9); 7.3192 (1.7); 7.3127 (1.4); 7.3064 (1.2); 7.2987 (14.4); 7.1089 (0.4); 7.0586 (0.7); 7.0153 (2.6); 6.9898 (3.0); 6.9244 (3.0); 6.7060 (1.6); 6.6817 (1.4); 6.2183 (2.1); 4.3836 (1.0); 4.3747 (1.3); 4.3487 (1.4); 4.3395 (1.4); 4.1709 (0.7); 4.1471 (0.7); 3.9700 (0.6); 3.9484 (0.8); 3.9440 (0.7); 3.9371 (0.9); 3.9269 (0.7); 3.9208 (0.8); 3.9030 (2.6); 3.8819 (1.0); 3.8683 (2.0); 3.8469 (1.3); 3.8362 (0.4); 3.0858 (1.0); 3.0718 (1.0); 3.0406 (1.4); 3.0254 (1.3); 2.7771 (1.4); 2.7446 (1.4); 2.7319 (1.2); 2.6988 (1.1); 2.3618 (1.6); 2.3512 (1.0); 2.3387 (2.2); 2.3155 (16.0); 2.2758 (0.4); 2.1828 (14.8); 2.0829 (3.6); 1.6485 (1.3); 1.3206 (1.0); 1.2968 (2.0); 1.2730 (0.9); 0.1082 (0.5); 0.0482 (0.6); 0.0374 (16.4); 0.0265 (0.6) I-159: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.4940 (8.2); 7.7014 (0.5); 7.6819 (5.2); 7.6590 (2.2); 7.6326 (0.7); 7.3703 (2.6); 7.3145 (1.2); 7.3069 (1.7); 7.2987 (7.7); 7.2924 (1.5); 7.2848 (1.7); 7.2774 (0.8); 6.9847 (2.5); 6.9593 (2.9); 6.9157 (3.0); 6.6783 (1.7); 6.6536 (1.4); 6.1265 (2.0); 4.3831 (1.2); 4.3737 (1.3); 4.3477 (1.4); 4.3383 (1.4); 3.9448 (0.6); 3.9293 (0.8); 3.9234 (0.8); 3.9116 (0.8); 3.9007 (0.6); 3.8953 (0.7); 3.8888 (0.6); 3.8805 (0.5); 3.8694 (2.4); 3.8479 (1.1); 3.8342 (1.9); 3.8127 (1.2); 3.0851 (1.0); 3.0706 (1.0); 3.0397 (1.4); 3.0247 (1.3); 2.7366 (1.5); 2.7033 (1.4); 2.6913 (1.2); 2.6575 (1.1); 2.3027 (16.0); 2.1679 (14.8); 1.5940 (1.8); 0.1091 (0.5); 0.0491 (0.4); 0.0385 (8.5); 0.0277 (0.4) I-160: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.9338 (4.8); 7.5181 (0.8); 7.5024 (2.0); 7.4865 (1.3); 7.4227 (1.6); 7.4073 (1.2); 7.2604 (3.1); 7.2056 (2.2); 7.1446 (1.2); 7.1423 (1.2); 7.1284 (1.1); 7.1261 (1.1); 6.9589 (2.1); 6.9436 (2.4); 6.8862 (2.5); 6.7753 (1.2); 6.6850 (1.4); 6.6694 (1.3); 6.6626 (2.7); 6.5497 (1.3); 6.1586 (1.6); 4.2517 (1.1); 4.2452 (1.2); 4.2302 (1.2); 4.2237 (1.2); 3.8719 (0.5); 3.8679 (0.5); 3.8622 (0.7); 3.8584 (0.6); 3.8521 (0.7); 3.8487 (0.6); 3.8451 (0.5); 3.8427 (0.5); 3.8041 (1.7); 3.7915 (1.1); 3.7825 (1.5); 3.7699 (1.1); 2.9866 (0.9); 2.9771 (1.0); 2.9592 (1.1); 2.9498 (1.2); 2.7112 (1.2); 2.6915 (1.2); 2.6839 (1.1); 2.6641 (1.0); 2.6575 (0.3); 2.6324 (16.0); 2.2577 (13.2); 2.1642 (12.4); 1.9988 (8.9); 1.6185 (0.4); −0.0002 (3.0) I-161: ¹H-NMR(499.9 MHz, CDCl3): δ = 9.7273 (0.4); 7.9335 (5.0); 7.5179 (0.8); 7.5022 (1.9); 7.4863 (1.3); 7.4227 (1.7); 7.4073 (1.2); 7.2606 (3.3); 7.2053 (2.2); 7.1441 (1.2); 7.1420 (1.2); 7.1279 (1.1); 7.1257 (1.1); 6.9587 (2.1); 6.9435 (2.4); 6.8862 (2.6); 6.7753 (1.2); 6.6850 (1.4); 6.6693 (1.4); 6.6625 (2.6); 6.5497 (1.2); 6.1582 (1.6); 4.2517 (1.1); 4.2452 (1.2); 4.2302 (1.2); 4.2236 (1.2); 3.8718 (0.5); 3.8623 (0.7); 3.8585 (0.7); 3.8521 (0.7); 3.8451 (0.6); 3.8429 (0.6); 3.8039 (1.6); 3.7913 (1.1); 3.7823 (1.4); 3.7697 (1.1); 2.9866 (0.9); 2.9771 (0.9); 2.9592 (1.1); 2.9498 (1.2); 2.7111 (1.2); 2.6914 (1.2); 2.6838 (1.1); 2.6639 (1.1); 2.6568 (0.8); 2.6321 (16.0); 2.3083 (0.6); 2.2577 (12.8); 2.1642 (12.1); 1.9990 (10.8); −0.0002 (3.3) I-162: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.1157 (16.0); 7.6279 (0.5); 7.6114 (8.6); 7.6012 (10.4); 7.5857 (0.3); 7.4499 (7.6); 7.4462 (7.8); 7.3769 (5.4); 7.2770 (0.6); 7.2690 (2.4); 7.2607 (20.0); 7.2513 (2.2); 7.2464 (1.6); 7.1025 (2.6); 7.0988 (2.5); 7.0862 (5.8); 7.0825 (5.9); 7.0603 (9.2); 7.0440 (4.0); 6.0336 (3.3); 4.1497 (2.9); 4.1434 (3.1); 4.1278 (3.5); 4.1216 (3.6); 4.0169 (0.5); 4.0069 (1.2); 4.0003 (1.8); 3.9907 (2.0); 3.9831 (1.9); 3.9770 (1.2); 3.9729 (1.0); 3.9666 (0.5); 3.9268 (3.8); 3.9173 (2.9); 3.9049 (3.1); 3.8955 (2.5); 3.7962 (0.4); 3.1210 (2.4); 3.1105 (2.4); 3.0939 (3.4); 3.0833 (3.2); 2.9674 (3.4); 2.9493 (3.4); 2.9403 (2.5); 2.9221 (2.4); 2.6088 (0.6); 2.3990 (0.4); 2.0028 (13.4); 1.5537 (2.3); 1.2554 (1.2); 0.8456 (0.4); −0.0002 (18.8); −0.0067 (0.7) I-163: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.1153 (16.0); 7.6280 (0.4); 7.6114 (8.6); 7.6011 (11.0); 7.5855 (0.4); 7.4498 (8.0); 7.4460 (8.5); 7.3767 (5.7); 7.2773 (0.5); 7.2694 (2.0); 7.2607 (21.2); 7.2517 (2.5); 7.2466 (1.8); 7.1025 (2.7); 7.0987 (2.6); 7.0862 (6.0); 7.0825 (6.2); 7.0720 (0.3); 7.0604 (9.6); 7.0441 (4.3); 6.0313 (3.2); 4.1495 (2.7); 4.1433 (3.2); 4.1276 (3.4); 4.1214 (3.7); 4.0169 (0.5); 4.0070 (1.1); 4.0005 (1.8); 3.9910 (1.9); 3.9834 (1.9); 3.9732 (1.1); 3.9669 (0.5); 3.9270 (3.7); 3.9176 (2.9); 3.9051 (3.0); 3.8957 (2.5); 3.1210 (2.5); 3.1104 (2.5); 3.0938 (3.5); 3.0833 (3.4); 2.9676 (3.4); 2.9495 (3.4); 2.9405 (2.6); 2.9223 (2.4); 2.6113 (0.6); 2.0026 (14.9); 1.5559 (1.7); 1.4318 (0.5); 1.2842 (0.4); 1.2554 (1.6); 1.2420 (0.3); 1.2147 (2.0); 1.2025 (1.9); 0.8586 (0.5); 0.8456 (0.7); 0.0772 (0.4); 0.0700 (9.6); 0.0628 (0.5); 0.0062 (0.7); −0.0002 (20.6); −0.0067 (1.0) I-164: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.1190 (8.7); 7.6120 (2.8); 7.6088 (2.2); 7.6032 (4.6); 7.6017 (5.2); 7.3536 (2.5); 7.2606 (8.1); 7.2117 (3.7); 7.2039 (1.6); 7.2001 (1.6); 7.1969 (0.9); 7.1939 (1.2); 7.1887 (0.9); 7.0098 (1.1); 7.0060 (1.1); 6.9936 (1.9); 6.9898 (2.0); 6.9514 (3.7); 6.9352 (2.2); 6.0439 (1.7); 4.2125 (0.8); 4.2077 (1.6); 4.1923 (1.6); 4.1874 (1.0); 3.8828 (0.5); 3.8773 (0.7); 3.8722 (0.7); 3.8670 (0.8); 3.8581 (2.3); 3.8487 (1.2); 3.8375 (2.0); 3.8265 (1.1); 2.9836 (0.9); 2.9790 (0.6); 2.9740 (0.9); 2.9562 (1.4); 2.9517 (0.6); 2.9464 (1.4); 2.7712 (1.1); 2.7624 (0.3); 2.7523 (1.1); 2.7436 (1.1); 2.7248 (1.0); 2.2805 (16.0); 2.0022 (11.9); 1.5574 (1.0); 1.2555 (0.3); −0.0002 (8.9); −0.0067 (0.5) I-165: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.1193 (8.3); 7.6296 (0.3); 7.6122 (3.2); 7.6089 (2.5); 7.6036 (4.6); 7.6019 (5.0); 7.3545 (2.5); 7.2606 (8.3); 7.2151 (3.3); 7.2118 (3.8); 7.2039 (1.5); 7.2000 (1.5); 7.1968 (0.8); 7.1938 (1.1); 7.1886 (0.8); 7.0097 (1.2); 7.0058 (1.1); 6.9935 (2.0); 6.9897 (1.9); 6.9514 (3.7); 6.9352 (2.1); 6.0440 (1.7); 4.2129 (0.9); 4.2081 (1.5); 4.1926 (1.6); 4.1880 (1.0); 3.8879 (0.3); 3.8828 (0.6); 3.8774 (0.8); 3.8722 (0.8); 3.8670 (1.0); 3.8583 (2.4); 3.8489 (1.1); 3.8376 (1.9); 3.8266 (1.0); 2.9837 (1.0); 2.9793 (0.6); 2.9741 (0.9); 2.9563 (1.5); 2.9465 (1.3); 2.7711 (1.1); 2.7618 (0.4); 2.7521 (1.2); 2.7435 (1.0); 2.7247 (0.9); 2.2806 (16.0); 2.0024 (11.8); 1.5566 (1.2); 1.2555 (0.5); 0.0062 (0.7); −0.0002 (9.1); −0.0068 (0.3) I-166: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.9800 (4.0); 7.6528 (1.6); 7.6368 (1.6); 7.5021 (0.3); 7.4846 (1.9); 7.4746 (3.6); 7.3536 (1.9); 7.3302 (1.7); 7.3207 (1.3); 7.3150 (2.6); 7.2592 (6.5); 7.2414 (1.4); 7.2252 (0.7); 7.0794 (3.8); 7.0548 (1.0); 7.0405 (1.5); 7.0248 (0.8); 6.1856 (1.4); 5.2969 (3.7); 5.0872 (0.7); 5.0789 (0.8); 5.0712 (0.8); 5.0628 (0.7); 4.4304 (0.9); 4.4219 (0.8); 4.4083 (1.0); 4.3999 (0.9); 4.0363 (1.1); 4.0199 (1.1); 4.0143 (1.1); 3.9980 (1.0); 3.7432 (12.5); 2.6938 (12.0); 2.0019 (16.0); 1.5663 (1.8); −0.0002 (6.4) I-167: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.9811 (5.0); 7.6528 (1.7); 7.6368 (1.8); 7.5022 (0.4); 7.4863 (2.0); 7.4841 (2.0); 7.4808 (1.8); 7.4760 (3.5); 7.4742 (3.7); 7.3531 (1.9); 7.3315 (1.8); 7.3200 (1.4); 7.3152 (2.9); 7.3099 (1.0); 7.3045 (0.5); 7.2584 (9.2); 7.2435 (1.3); 7.2417 (1.6); 7.2271 (0.8); 7.2254 (0.7); 7.0793 (4.4); 7.0566 (1.0); 7.0551 (1.1); 7.0409 (1.7); 7.0266 (0.8); 7.0251 (0.8); 6.1856 (1.5); 5.2966 (5.4); 5.0893 (0.8); 5.0870 (0.8); 5.0810 (0.8); 5.0785 (0.8); 5.0732 (0.8); 5.0708 (0.8); 5.0647 (0.7); 5.0625 (0.7); 4.4320 (0.9); 4.4308 (0.9); 4.4238 (0.9); 4.4224 (0.9); 4.4101 (1.0); 4.4088 (1.0); 4.4017 (0.9); 4.0362 (1.4); 4.0199 (1.4); 4.0142 (1.3); 3.9979 (1.2); 3.7434 (16.0); 2.6940 (15.3); 1.5617 (1.5); 0.0061 (0.7); −0.0002 (9.3); −0.0066 (0.4) I-168: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.2557 (2.7); 8.2516 (3.0); 7.9074 (5.3); 7.7310 (3.1); 7.7269 (3.2); 7.5203 (0.5); 7.5111 (2.2); 7.5067 (2.2); 7.4897 (1.9); 7.4749 (2.1); 7.4700 (1.9); 7.4649 (2.0); 7.4504 (0.9); 7.2318 (1.4); 7.1902 (31.8); 5.2290 (11.7); 5.0100 (0.6); 5.0025 (0.9); 4.9964 (0.8); 4.9940 (0.9); 4.9864 (0.9); 4.9803 (0.7); 4.7926 (1.2); 4.7848 (1.2); 4.7717 (1.3); 4.7638 (1.2); 4.0730 (0.4); 4.0587 (1.2); 4.0444 (1.2); 4.0301 (0.4); 3.2432 (1.3); 3.2268 (1.4); 3.2223 (1.5); 3.2059 (1.3); 2.6335 (16.0); 2.2104 (0.3); 1.9741 (5.4); 1.9358 (4.1); 1.4856 (2.6); 1.2233 (0.4); 1.2142 (0.4); 1.2032 (1.8); 1.1889 (4.1); 1.1845 (2.9); 1.1747 (1.9); 1.1627 (0.4); 1.0994 (0.4); 1.0959 (0.4); 1.0867 (0.5); 1.0832 (0.5); 1.0629 (0.3); 0.8101 (0.5); 0.1164 (0.4); −0.0002 (89.6); −0.0638 (1.1); −0.0703 (34.5); −0.0765 (2.9); −0.1196 (0.6) I-169: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9111 (1.1); 7.9004 (1.1); 7.6445 (0.4); 7.6184 (1.5); 7.5972 (4.4); 7.5809 (0.8); 7.4673 (2.4); 7.4407 (1.0); 7.4320 (1.5); 7.4247 (1.0); 7.4112 (1.0); 7.4033 (0.6); 7.2983 (9.1); 7.0593 (1.8); 7.0332 (5.3); 6.9629 (1.7); 6.9360 (1.0); 5.3359 (1.0); 4.6975 (1.5); 4.2290 (0.4); 4.2125 (1.2); 4.1865 (1.4); 4.1700 (0.6); 3.9993 (0.8); 3.9840 (2.1); 3.9561 (1.8); 3.4764 (0.4); 3.0485 (0.4); 3.0324 (0.5); 3.0028 (1.2); 2.9866 (1.2); 2.9551 (1.2); 2.9383 (1.1); 2.9264 (2.1); 2.9140 (1.5); 2.9024 (1.1); 2.8834 (16.0); 2.8174 (1.7); 2.5233 (0.6); 2.3283 (14.0); 2.3172 (13.6); 1.7869 (0.3); 1.6704 (0.6); 1.2915 (0.4); 0.9114 (0.6); 0.8877 (2.5); 0.8695 (2.5); 0.8641 (2.0); 0.8465 (0.8); 0.6380 (0.8); 0.6239 (1.9); 0.6207 (2.1); 0.6143 (2.1); 0.6077 (2.0); 0.6034 (1.9); 0.5847 (0.6); 0.1071 (0.6); 0.0474 (0.4); 0.0366 (9.9); 0.0259 (0.4) I-170: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.2165 (16.0); 8.0518 (0.3); 7.3659 (6.9); 7.3589 (7.1); 7.2985 (23.7); 7.1937 (5.7); 7.1664 (8.3); 7.1391 (3.9); 7.1104 (3.7); 7.0889 (2.6); 7.0825 (3.3); 7.0653 (2.8); 7.0600 (3.4); 7.0406 (3.9); 7.0329 (1.7); 7.0040 (3.5); 6.9816 (3.9); 6.9453 (7.6); 6.9388 (4.7); 6.9186 (3.5); 6.9115 (3.4); 6.8823 (1.9); 6.8762 (1.9); 6.8561 (3.0); 6.8341 (1.7); 6.8287 (1.6); 6.2618 (6.3); 6.2023 (7.7); 5.6757 (6.2); 5.6384 (5.8); 4.2157 (2.3); 4.2056 (2.9); 4.1940 (0.5); 4.1800 (3.2); 4.1701 (4.2); 4.1464 (0.7); 4.0792 (0.4); 4.0630 (1.0); 4.0526 (1.6); 4.0367 (1.8); 4.0231 (1.8); 4.0137 (1.1); 4.0066 (1.2); 3.9883 (4.1); 3.9730 (2.2); 3.9528 (2.9); 3.9372 (2.0); 3.2175 (2.1); 3.2010 (2.1); 3.1728 (3.2); 3.1560 (3.0); 3.0166 (3.1); 2.9927 (3.3); 2.9870 (3.2); 2.9719 (2.2); 2.9417 (2.1); 2.9206 (2.4); 2.1596 (0.6); 2.1422 (1.2); 2.1311 (1.3); 2.1140 (2.4); 2.0968 (1.5); 2.0824 (3.7); 2.0686 (0.8); 1.6048 (10.8); 1.3674 (0.4); 1.3437 (0.9); 1.3200 (2.2); 1.3034 (5.6); 1.2965 (6.0); 1.2726 (1.2); 1.0968 (1.1); 1.0932 (1.2); 1.0823 (4.1); 1.0755 (4.9); 1.0650 (2.8); 1.0610 (2.2); 1.0536 (4.4); 1.0473 (4.5); 1.0366 (1.7); 1.0330 (1.6); 1.0156 (0.3); 0.9405 (2.0); 0.9187 (6.2); 0.8955 (2.4); 0.8721 (0.3); 0.8570 (0.4); 0.8351 (2.4); 0.8287 (2.4); 0.8199 (4.9); 0.8123 (4.9); 0.8033 (5.6); 0.7960 (3.4); 0.7864 (2.0); 0.7653 (0.4); 0.1069 (1.6); 0.0476 (0.9); 0.0367 (27.9); 0.0259 (1.2) I-171: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.7047 (5.9); 7.3638 (2.4); 7.3568 (2.4); 7.2983 (9.5); 7.2052 (0.6); 7.1955 (2.0); 7.1784 (1.4); 7.1743 (1.4); 7.1683 (2.5); 7.1516 (1.0); 7.1485 (1.0); 7.0983 (0.8); 7.0925 (0.9); 7.0744 (0.9); 7.0695 (1.1); 7.0477 (0.5); 7.0423 (0.5); 6.9592 (1.4); 6.9521 (1.4); 6.9320 (1.2); 6.9246 (1.6); 6.9181 (0.7); 6.8965 (1.1); 6.8750 (0.5); 6.8697 (0.5); 5.9875 (1.0); 5.9804 (1.0); 4.2173 (0.7); 4.2075 (0.9); 4.1817 (1.1); 4.1721 (1.2); 4.0697 (0.3); 4.0587 (0.5); 4.0428 (0.6); 4.0294 (0.6); 4.0217 (0.4); 4.0132 (0.4); 4.0029 (1.5); 3.9877 (0.7); 3.9671 (0.9); 3.9520 (0.7); 3.2195 (0.7); 3.2032 (0.7); 3.1749 (1.1); 3.1580 (1.0); 3.0299 (1.0); 3.0005 (1.0); 2.9853 (0.7); 2.9553 (0.7); 2.8133 (16.0); 2.1621 (0.4); 2.1508 (0.4); 2.1338 (0.8); 2.1164 (0.5); 2.1055 (0.4); 1.5939 (8.3); 1.3033 (1.1); 1.1217 (0.4); 1.1183 (0.4); 1.1070 (1.4); 1.1001 (1.6); 1.0896 (0.9); 1.0854 (0.7); 1.0783 (1.5); 1.0719 (1.5); 1.0607 (0.5); 1.0574 (0.5); 0.9398 (0.4); 0.9183 (1.3); 0.8951 (0.5); 0.8541 (0.8); 0.8467 (0.8); 0.8381 (1.6); 0.8314 (1.5); 0.8219 (1.8); 0.8151 (1.1); 0.8046 (0.6); 0.1064 (0.8); 0.0470 (0.3); 0.0362 (11.2); 0.0270 (0.4); 0.0254 (0.5) I-172: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9751 (0.4); 7.9587 (9.7); 7.3650 (5.0); 7.3580 (5.0); 7.2986 (22.6); 7.1915 (4.0); 7.1642 (5.0); 7.1556 (1.5); 7.1283 (3.0); 7.1004 (2.8); 7.0838 (2.1); 7.0773 (2.4); 7.0602 (2.1); 7.0550 (2.4); 7.0336 (1.2); 7.0278 (1.0); 6.9428 (3.0); 6.9357 (2.8); 6.9155 (2.5); 6.9085 (2.4); 6.8686 (1.4); 6.8620 (1.4); 6.8445 (2.3); 6.8202 (1.3); 6.8151 (1.2); 6.2138 (2.1); 4.2037 (1.7); 4.1938 (2.2); 4.1690 (2.7); 4.1580 (2.6); 4.1468 (1.2); 4.1234 (0.5); 4.0699 (0.4); 4.0534 (0.8); 4.0426 (1.2); 4.0271 (1.4); 4.0135 (1.4); 4.0067 (1.0); 3.9972 (1.0); 3.9877 (0.7); 3.9760 (2.9); 3.9605 (1.7); 3.9402 (2.1); 3.9247 (1.5); 3.2112 (1.5); 3.1945 (1.5); 3.1663 (2.3); 3.1496 (2.2); 3.0271 (2.3); 3.0095 (2.9); 3.0018 (7.1); 2.9766 (7.9); 2.9656 (2.1); 2.9512 (2.6); 2.9350 (1.6); 2.9219 (0.5); 2.1568 (0.4); 2.1403 (1.0); 2.1293 (1.1); 2.1122 (1.9); 2.0950 (1.3); 2.0828 (5.9); 2.0667 (0.6); 1.6148 (2.5); 1.4036 (7.7); 1.3783 (16.0); 1.3529 (7.3); 1.3203 (1.3); 1.2965 (2.6); 1.2727 (1.2); 1.2154 (0.4); 1.1480 (0.4); 1.0921 (1.0); 1.0880 (1.0); 1.0773 (3.2); 1.0709 (3.7); 1.0605 (2.2); 1.0562 (1.9); 1.0488 (3.4); 1.0427 (3.4); 1.0322 (1.4); 1.0282 (1.3); 0.9962 (0.4); 0.9723 (0.5); 0.8534 (0.4); 0.8310 (1.9); 0.8247 (2.0); 0.8160 (3.7); 0.8083 (3.8); 0.7993 (4.2); 0.7919 (2.6); 0.7826 (1.5); 0.7618 (0.4); 0.1065 (2.1); 0.0474 (1.0); 0.0367 (23.3); 0.0258 (1.2) I-173: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.0750 (10.2); 7.5797 (0.4); 7.5743 (0.7); 7.5721 (0.7); 7.5616 (5.6); 7.5567 (1.8); 7.5488 (2.2); 7.5330 (0.5); 7.3157 (2.5); 7.2584 (10.3); 7.2355 (1.0); 7.2313 (1.4); 7.2266 (0.7); 7.2244 (0.7); 7.2221 (1.3); 7.2178 (1.7); 7.2126 (0.7); 6.9483 (2.7); 6.9331 (2.8); 6.8612 (2.8); 6.6324 (1.6); 6.6172 (1.4); 5.7973 (1.9); 5.3681 (1.4); 5.2968 (2.2); 3.9547 (0.3); 3.9459 (0.7); 3.9418 (0.7); 3.9381 (0.8); 3.9320 (0.7); 3.9263 (0.8); 3.9224 (0.6); 3.9183 (0.6); 3.3820 (1.2); 3.3747 (1.2); 3.3606 (1.3); 3.3533 (1.2); 2.9929 (1.3); 2.9855 (2.2); 2.9730 (1.7); 2.9647 (2.5); 2.9563 (1.4); 2.9516 (1.5); 2.6989 (1.5); 2.6792 (1.5); 2.6717 (1.3); 2.6520 (1.2); 2.2512 (16.0); 2.1429 (14.8); 1.5545 (3.0); 0.0063 (0.7); −0.0002 (12.8); −0.0069 (0.4) I-174: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.2988 (1.7); 7.2858 (0.4); 7.2716 (0.7); 7.2672 (0.7); 7.2586 (0.7); 7.2522 (0.8); 7.2430 (0.6); 7.2361 (0.6); 7.2293 (0.6); 7.2239 (0.7); 7.2126 (0.7); 7.1962 (1.0); 7.1862 (1.0); 7.1695 (0.5); 7.1593 (0.5); 7.1255 (0.8); 7.1030 (1.1); 7.0796 (0.5); 7.0528 (0.8); 7.0416 (0.9); 7.0162 (3.6); 6.9458 (1.5); 6.9201 (0.9); 5.3334 (2.0); 4.9457 (0.8); 4.9061 (0.8); 4.2042 (0.5); 4.1782 (0.7); 4.1695 (0.6); 4.1588 (0.6); 4.1327 (0.7); 3.9242 (1.4); 3.9023 (1.3); 3.8966 (1.3); 3.8787 (0.4); 3.8700 (0.6); 3.8517 (0.3); 3.0245 (0.5); 3.0073 (0.5); 2.9790 (1.0); 2.9614 (0.9); 2.9093 (0.6); 2.8818 (1.1); 2.8650 (1.0); 2.8523 (1.0); 2.8363 (1.0); 2.8254 (0.7); 2.8080 (0.5); 2.5437 (7.4); 2.5354 (7.6); 2.3073 (16.0); 1.9572 (0.6); 1.9401 (0.5); 1.9343 (0.5); 1.9173 (0.6); 1.7314 (0.4); 1.7185 (0.6); 1.7070 (0.6); 1.6904 (0.6); 1.6786 (0.6); 1.6662 (0.5); 1.6511 (0.4); 0.0413 (1.7) I-175: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.1195 (16.0); 7.6182 (0.4); 7.6034 (1.7); 7.5876 (5.7); 7.5816 (5.2); 7.5658 (4.7); 7.5502 (2.0); 7.5190 (0.4); 7.4077 (6.5); 7.3915 (9.2); 7.3626 (0.4); 7.3384 (5.3); 7.3098 (8.6); 7.2936 (6.3); 7.2606 (13.4); 7.1951 (2.8); 7.1799 (2.9); 7.1768 (2.0); 6.0747 (3.3); 4.2144 (2.4); 4.2084 (2.9); 4.1930 (3.1); 4.1871 (3.1); 3.9386 (0.4); 3.9324 (0.6); 3.9279 (1.1); 3.9222 (1.5); 3.9172 (1.5); 3.9125 (1.6); 3.9090 (1.6); 3.9036 (1.6); 3.8982 (1.3); 3.8934 (1.4); 3.8849 (4.5); 3.8742 (2.0); 3.8635 (3.5); 3.8528 (2.4); 3.0894 (2.0); 3.0797 (2.0); 3.0625 (2.5); 3.0526 (2.4); 2.8706 (2.7); 2.8519 (2.6); 2.8438 (2.3); 2.8248 (2.1); 1.5603 (13.3); 0.0063 (0.5); −0.0002 (14.7); −0.0066 (0.7) I-176: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.5785 (1.0); 7.5541 (2.1); 7.5236 (0.3); 7.4362 (1.4); 7.4208 (0.8); 7.4141 (1.0); 7.4074 (0.5); 7.3900 (0.6); 7.2987 (7.1); 7.0418 (1.2); 7.0276 (1.7); 7.0168 (2.0); 6.9547 (1.1); 6.9293 (0.6); 4.6790 (1.0); 4.2087 (0.8); 4.1829 (1.0); 3.9618 (0.5); 3.9391 (1.3); 3.9086 (1.0); 3.8914 (0.4); 3.0338 (0.4); 3.0180 (0.4); 2.9879 (0.8); 2.9716 (0.7); 2.9056 (0.7); 2.8756 (0.6); 2.8601 (0.4); 2.8296 (0.4); 2.6636 (12.4); 2.4262 (12.0); 2.3187 (16.0); 1.5962 (0.3); 0.1200 (0.6); 0.1082 (10.9); 0.0959 (0.6); 0.0489 (0.5); 0.0381 (9.0); 0.0274 (0.4) I-177: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1047 (3.8); 7.6302 (0.7); 7.6045 (9.5); 7.5800 (4.1); 7.5496 (0.9); 7.5306 (2.7); 7.4646 (5.7); 7.4454 (1.3); 7.2986 (19.1); 7.0484 (3.1); 7.0039 (0.7); 6.9679 (5.2); 6.9417 (0.7); 5.8345 (2.0); 4.1620 (0.4); 4.1422 (1.4); 4.1174 (1.7); 4.0972 (0.6); 3.8625 (0.9); 3.8432 (2.6); 3.8278 (1.6); 3.8197 (2.4); 3.8008 (0.8); 2.9570 (0.7); 2.9388 (0.7); 2.9110 (1.3); 2.8926 (1.2); 2.8047 (1.2); 2.7784 (1.2); 2.7586 (0.7); 2.7326 (0.7); 2.3389 (15.0); 2.3200 (16.0); 2.2962 (0.7); 2.1853 (14.1); 1.5955 (6.9); 1.3715 (0.3); 1.3224 (0.5); 1.2931 (1.8); 1.2605 (0.4); 0.8940 (0.5); 0.8779 (0.4); 0.8692 (0.5); 0.1078 (1.8); 0.0380 (17.5); 0.0273 (0.9) I-178: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.5813 (1.0); 7.5568 (2.0); 7.5525 (1.8); 7.4325 (1.4); 7.4168 (0.7); 7.4104 (1.0); 7.4035 (0.5); 7.3943 (0.4); 7.3859 (0.6); 7.2986 (11.4); 7.0383 (1.2); 7.0276 (1.6); 7.0138 (1.9); 6.9541 (1.0); 6.9284 (0.6); 6.0502 (0.5); 6.0168 (0.8); 5.9938 (0.8); 5.9603 (0.6); 5.3793 (0.4); 5.3749 (1.1); 5.3703 (1.1); 5.3183 (0.9); 5.3138 (0.9); 5.3095 (0.4); 5.1848 (1.0); 5.1804 (1.0); 5.1514 (0.9); 5.1471 (0.9); 4.6572 (1.0); 4.2069 (0.8); 4.1811 (0.9); 3.9819 (2.4); 3.9787 (1.8); 3.9591 (2.6); 3.9556 (1.9); 3.9377 (1.2); 3.9140 (0.4); 3.9070 (1.0); 3.8901 (0.4); 3.0315 (0.4); 3.0153 (0.4); 2.9852 (0.7); 2.9692 (0.7); 2.9026 (0.6); 2.8726 (0.6); 2.8573 (0.4); 2.8263 (0.3); 2.4189 (12.6); 2.3181 (16.0); 1.5980 (1.2); 0.1075 (0.9); 0.0487 (0.4); 0.0378 (13.0); 0.0270 (0.5) I-179: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.0923 (8.6); 7.6036 (0.4); 7.5877 (2.2); 7.5825 (1.9); 7.5797 (2.0); 7.5762 (5.3); 7.5744 (5.4); 7.5007 (2.6); 7.4372 (0.9); 7.4310 (1.5); 7.4266 (1.5); 7.4189 (1.2); 7.4141 (0.8); 7.2588 (5.5); 7.2181 (2.8); 7.2023 (3.1); 6.9924 (2.8); 6.9089 (1.5); 6.9076 (1.5); 6.8933 (1.4); 6.8920 (1.4); 6.7314 (1.7); 4.1307 (1.3); 4.1238 (1.5); 4.1086 (1.7); 4.1017 (1.7); 3.8850 (1.6); 3.8743 (1.8); 3.8629 (1.4); 3.8521 (1.6); 3.6649 (0.5); 3.6594 (0.7); 3.6572 (0.7); 3.6503 (0.9); 3.6412 (0.8); 3.6358 (0.6); 3.1578 (1.5); 3.1485 (1.6); 3.1306 (1.8); 3.1212 (1.8); 2.8608 (1.7); 2.8420 (1.7); 2.8335 (1.6); 2.8148 (1.4); 2.3860 (0.4); 2.2862 (16.0); 2.2623 (15.6); 0.0710 (0.4); −0.0002 (6.1); −0.0066 (0.4) I-180: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.7251 (1.0); 7.6237 (0.5); 7.6081 (2.0); 7.5940 (4.9); 7.5800 (0.5); 7.4353 (2.6); 7.4001 (1.0); 7.3961 (1.6); 7.3822 (1.2); 7.3682 (0.5); 7.3523 (0.4); 7.2596 (9.2); 7.0813 (0.6); 7.0035 (2.4); 6.9950 (3.3); 6.9891 (3.2); 6.9209 (1.9); 6.9055 (1.4); 5.2980 (1.7); 4.6981 (2.0); 4.1913 (1.4); 4.1847 (0.6); 4.1755 (1.6); 4.1657 (0.6); 4.1550 (0.5); 4.1429 (0.4); 3.9415 (2.5); 3.9235 (1.8); 3.9136 (0.7); 3.4298 (16.0); 3.0029 (0.8); 2.9934 (0.8); 2.9751 (1.2); 2.9655 (1.1); 2.8886 (1.1); 2.8707 (1.1); 2.8613 (0.8); 2.8427 (0.7); 2.8020 (15.4); 2.4847 (1.4); 2.3464 (2.0); 2.2881 (14.9); 2.2812 (13.5); 2.1644 (0.8); 2.0397 (0.7); 1.5484 (2.2); 1.2568 (0.6); −0.0002 (10.3) I-181: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.1255 (7.3); 7.5722 (0.6); 7.5643 (3.7); 7.5625 (4.3); 7.5570 (1.6); 7.5503 (1.8); 7.5345 (0.4); 7.3179 (2.1); 7.2585 (8.0); 7.2422 (0.9); 7.2379 (1.1); 7.2329 (0.6); 7.2292 (1.1); 7.2248 (1.2); 7.2193 (0.6); 6.9353 (2.1); 6.9200 (2.3); 6.8670 (2.3); 6.6343 (1.3); 6.6193 (1.1); 5.8391 (0.9); 3.9805 (0.6); 3.9720 (0.6); 3.1553 (0.8); 3.1479 (0.8); 3.1335 (0.9); 3.1263 (0.8); 2.9821 (1.1); 2.9725 (1.1); 2.9548 (1.4); 2.9380 (16.0); 2.6823 (1.2); 2.6627 (1.2); 2.6551 (1.1); 2.6356 (1.0); 2.6195 (1.4); 2.6065 (1.4); 2.5976 (1.3); 2.5847 (1.2); 2.2760 (0.5); 2.2452 (12.8); 2.1515 (11.7); 0.0699 (0.6); 0.0062 (0.5); −0.0002 (8.6) I-182: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.1228 (9.3); 7.5650 (0.8); 7.5572 (4.5); 7.5555 (5.6); 7.5503 (2.0); 7.5431 (2.3); 7.5273 (0.5); 7.3565 (0.4); 7.3124 (2.7); 7.2582 (12.1); 7.2329 (1.1); 7.2288 (1.5); 7.2239 (0.8); 7.2199 (1.4); 7.2156 (1.6); 7.2101 (0.8); 6.9374 (2.7); 6.9221 (2.8); 6.8645 (3.0); 6.6315 (1.6); 6.6166 (1.4); 5.7947 (0.8); 3.9664 (0.7); 3.1671 (0.8); 3.1491 (1.8); 3.1349 (3.0); 3.1206 (2.8); 3.1065 (1.0); 2.9815 (1.0); 2.9719 (1.0); 2.9543 (1.2); 2.9448 (1.1); 2.6713 (1.4); 2.6589 (1.8); 2.6518 (1.7); 2.6456 (2.5); 2.6373 (1.7); 2.6244 (2.5); 2.2914 (0.7); 2.2456 (16.0); 2.2122 (0.7); 2.1496 (14.7); 1.3100 (3.3); 1.2958 (6.4); 1.2816 (3.1); 1.2712 (0.4); 1.0585 (0.4); 0.0062 (1.0); −0.0002 (14.5); −0.0068 (0.6) I-183: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1668 (16.0); 7.6526 (0.8); 7.6388 (8.2); 7.6357 (9.3); 7.6154 (4.3); 7.5891 (1.1); 7.3838 (4.5); 7.2983 (33.3); 7.2874 (2.4); 7.2797 (2.8); 7.2646 (3.1); 7.2543 (9.2); 7.2256 (10.0); 7.0435 (6.7); 7.0171 (5.3); 6.1203 (3.3); 5.3377 (5.5); 4.2605 (2.8); 4.2348 (3.2); 4.2274 (1.6); 4.2167 (0.8); 3.9614 (0.3); 3.9432 (0.9); 3.9331 (1.3); 3.9253 (1.5); 3.9103 (4.3); 3.9024 (3.9); 3.8764 (3.8); 3.8579 (1.8); 3.0841 (1.7); 3.0697 (1.6); 3.0390 (2.7); 3.0237 (2.5); 2.8493 (2.2); 2.8332 (0.7); 2.8182 (2.2); 2.8044 (1.8); 2.7731 (1.6); 1.5856 (12.7); 1.3466 (0.5); 1.2925 (1.1); 0.9180 (0.3); 0.1069 (5.2); 0.0478 (1.5); 0.0371 (44.2); 0.0262 (1.9); −0.0297 (0.4) I-184: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 10.1012 (5.6); 8.2715 (16.0); 7.8018 (5.5); 7.7810 (14.2); 7.7760 (8.8); 7.7625 (3.8); 7.7422 (4.5); 7.7307 (5.9); 7.7234 (5.3); 7.7038 (2.2); 7.6876 (3.6); 7.6686 (2.1); 7.4753 (3.7); 7.4700 (3.6); 7.4542 (3.3); 7.4488 (3.3); 5.5264 (1.7); 5.5161 (1.9); 5.4964 (2.0); 5.4854 (1.8); 3.8482 (1.8); 3.8377 (2.0); 3.8142 (2.4); 3.8038 (2.2); 3.5946 (2.4); 3.5636 (3.1); 3.5303 (2.0); 3.3414 (13.7); 2.6716 (0.4); 2.5069 (50.8); 2.5025 (68.1); 2.4980 (50.1); 2.3336 (0.4); 2.3293 (0.4); 0.0080 (0.4); 0.0001 (8.2) I-185: ¹H-NMR(300.1 MHz, d₆-DMSO): δ = 11.0094 (5.2); 8.2358 (16.0); 8.1566 (0.6); 7.8011 (5.9); 7.7774 (1.1); 7.7518 (3.4); 7.7263 (5.7); 7.7094 (5.9); 7.6891 (5.8); 7.6643 (2.1); 7.5211 (6.5); 7.4927 (12.4); 7.4339 (14.4); 7.4055 (7.4); 5.0679 (2.0); 5.0498 (2.3); 5.0250 (2.5); 5.0069 (2.1); 3.3270 (1.5); 2.7891 (1.9); 2.7707 (2.1); 2.7343 (3.2); 2.7160 (2.8); 2.5516 (3.1); 2.5079 (33.8); 2.5022 (41.1); 2.4966 (30.5); 2.4538 (2.2); 2.0755 (3.5); −0.0005 (5.8) I-186: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.1261 (10.9); 7.9532 (1.6); 7.6102 (1.0); 7.6062 (1.1); 7.5936 (1.2); 7.5896 (2.2); 7.5860 (1.4); 7.5738 (1.2); 7.5694 (1.2); 7.4468 (0.9); 7.4427 (1.0); 7.4297 (3.0); 7.4259 (3.7); 7.4221 (3.5); 7.4092 (1.8); 7.4048 (1.4); 7.3784 (1.8); 7.3753 (1.7); 7.3581 (2.2); 7.3548 (2.3); 7.3377 (0.8); 7.3342 (0.8); 7.0562 (2.7); 7.0371 (3.2); 6.9243 (3.3); 6.8250 (1.8); 6.8060 (1.5); 3.7625 (6.4); 3.7520 (1.2); 3.7434 (1.2); 3.7342 (1.0); 3.7250 (0.8); 3.7163 (0.5); 3.3321 (34.6); 2.8915 (11.2); 2.8527 (0.4); 2.8348 (0.4); 2.8180 (1.6); 2.8045 (2.7); 2.7883 (1.9); 2.7711 (0.4); 2.7323 (9.5); 2.5258 (0.7); 2.5209 (1.1); 2.5123 (13.2); 2.5079 (26.0); 2.5033 (33.7); 2.4988 (24.5); 2.4943 (11.9); 2.2407 (16.0); 2.1887 (14.6); −0.0002 (6.2) I-187: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.5821 (1.0); 7.5574 (2.0); 7.5527 (1.8); 7.5273 (0.3); 7.4362 (1.4); 7.4156 (0.7); 7.4087 (1.0); 7.4023 (0.5); 7.3896 (0.5); 7.3838 (0.6); 7.2983 (6.6); 7.0382 (1.3); 7.0267 (1.7); 7.0134 (1.9); 6.9532 (1.0); 6.9270 (0.6); 4.6657 (1.0); 4.2026 (0.8); 4.1768 (0.9); 3.9376 (1.3); 3.9084 (1.0); 3.8915 (0.4); 3.7231 (1.1); 3.7024 (3.0); 3.6838 (2.0); 3.5541 (2.0); 3.5348 (2.8); 3.5161 (1.0); 3.3973 (15.2); 3.0300 (0.4); 3.0142 (0.4); 2.9838 (0.7); 2.9678 (0.6); 2.9051 (0.6); 2.8755 (0.6); 2.8598 (0.4); 2.4285 (12.0); 2.3174 (16.0); 1.6183 (0.5); 0.1075 (0.6); 0.0373 (6.7) I-188: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1487 (16.0); 8.0661 (1.0); 7.9641 (0.4); 7.6337 (14.9); 7.6204 (9.3); 7.5880 (1.9); 7.5348 (0.8); 7.5091 (0.6); 7.4441 (0.7); 7.3817 (8.9); 7.3435 (1.1); 7.2985 (9.3); 7.2789 (6.0); 7.2668 (5.7); 7.2598 (5.6); 7.2139 (12.5); 7.1860 (14.4); 7.1564 (1.8); 7.1269 (1.4); 7.1048 (1.4); 7.0827 (1.2); 7.0536 (0.7); 7.0325 (0.7); 7.0046 (0.8); 6.9449 (13.7); 6.9173 (11.0); 6.8539 (0.4); 6.7847 (0.4); 6.6385 (4.1); 6.5391 (0.6); 6.3933 (8.1); 6.2928 (0.4); 6.1479 (6.0); 6.1301 (7.0); 5.3349 (0.6); 4.2616 (4.6); 4.2357 (5.3); 4.1693 (0.4); 4.0366 (0.4); 4.0094 (0.5); 3.8795 (8.6); 3.8464 (5.2); 3.8273 (3.0); 3.7955 (0.8); 3.7618 (0.4); 3.0621 (3.1); 3.0478 (3.1); 3.0176 (4.7); 3.0019 (4.2); 2.9611 (0.4); 2.9155 (0.6); 2.8958 (0.8); 2.8711 (0.5); 2.8051 (3.7); 2.7739 (3.8); 2.7603 (3.5); 2.7291 (2.8); 1.6319 (6.7); 1.2900 (0.7); 0.1080 (1.8); 0.0354 (8.2) I-189: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.2358 (6.4); 7.4223 (0.7); 7.4143 (0.7); 7.3974 (1.2); 7.3897 (1.0); 7.3743 (1.0); 7.3681 (1.0); 7.2986 (10.7); 7.2206 (0.7); 7.2163 (0.5); 7.1932 (1.8); 7.1889 (1.6); 7.1658 (3.1); 7.1578 (1.5); 7.1447 (1.2); 7.1385 (1.5); 7.1173 (0.6); 7.1111 (0.5); 7.0280 (1.6); 7.0214 (2.1); 6.9953 (2.6); 6.9689 (1.6); 6.9321 (1.6); 6.9102 (2.3); 6.7312 (1.3); 6.7061 (1.0); 6.2635 (2.8); 6.2044 (2.4); 6.0891 (1.5); 5.6836 (2.7); 5.6467 (2.5); 4.3355 (0.9); 4.3258 (1.1); 4.3010 (1.1); 4.2909 (1.1); 4.1946 (1.2); 4.1708 (3.5); 4.1470 (3.5); 4.1232 (1.2); 3.9478 (0.4); 3.9309 (0.6); 3.9256 (0.6); 3.9199 (0.6); 3.9149 (0.7); 3.8989 (0.6); 3.8915 (0.6); 3.8812 (2.1); 3.8604 (0.7); 3.8463 (1.5); 3.8255 (1.0); 3.0598 (0.8); 3.0443 (0.8); 3.0148 (1.1); 2.9985 (1.0); 2.7882 (1.2); 2.7567 (1.1); 2.7432 (0.9); 2.7110 (0.8); 2.3124 (12.7); 2.1859 (11.9); 2.0831 (16.0); 1.6073 (6.4); 1.3205 (4.3); 1.2967 (8.9); 1.2729 (4.1); 0.9190 (0.7); 0.0475 (0.4); 0.0368 (13.3); 0.0259 (0.5) I-190: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.8522 (5.3); 7.2856 (0.7); 7.2820 (0.8); 7.2696 (1.5); 7.2664 (1.0); 7.2565 (0.9); 7.2534 (0.9); 7.1890 (5.2); 7.0843 (0.7); 7.0818 (0.7); 7.0678 (1.6); 7.0654 (1.7); 7.0495 (1.4); 7.0372 (1.1); 7.0337 (1.2); 7.0240 (1.1); 7.0210 (1.5); 7.0077 (0.6); 7.0047 (0.6); 6.9004 (2.1); 6.8851 (2.4); 6.7973 (2.7); 6.6168 (1.4); 6.6017 (1.3); 5.9699 (1.7); 4.1921 (1.1); 4.1856 (1.2); 4.1706 (1.2); 4.1640 (1.3); 3.8143 (0.5); 3.8042 (0.8); 3.8007 (0.7); 3.7948 (0.8); 3.7849 (0.6); 3.7748 (0.3); 3.7462 (1.6); 3.7337 (1.1); 3.7246 (1.4); 3.7121 (1.1); 2.9231 (0.9); 2.9132 (1.0); 2.8958 (1.2); 2.8858 (1.1); 2.6614 (1.2); 2.6419 (1.2); 2.6343 (1.1); 2.6146 (0.9); 2.5625 (16.0); 2.5522 (0.7); 2.2313 (0.4); 2.1965 (13.2); 2.0772 (12.4); 1.9725 (1.7); 1.1870 (0.8); 0.8644 (0.4); −0.0002 (6.5); −0.0712 (6.2) I-192: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9700 (5.3); 7.2984 (10.0); 7.1265 (1.0); 7.1020 (2.4); 7.0711 (3.3); 7.0433 (3.3); 6.9991 (4.1); 6.8461 (1.2); 6.8231 (2.0); 6.8010 (1.2); 6.7718 (2.1); 6.7466 (1.8); 6.3163 (2.5); 5.3375 (0.5); 4.2789 (1.6); 4.2538 (1.7); 4.1710 (0.7); 4.1474 (0.6); 4.1243 (0.7); 4.1019 (1.0); 4.0797 (0.6); 3.8670 (2.9); 3.8345 (1.8); 3.8147 (0.9); 3.0478 (1.0); 3.0342 (1.0); 3.0035 (1.6); 2.9892 (1.4); 2.8809 (0.4); 2.8538 (0.9); 2.8271 (1.5); 2.7924 (1.9); 2.7602 (1.4); 2.7454 (1.3); 2.7149 (1.2); 2.6672 (16.0); 2.3330 (14.1); 2.1703 (0.6); 2.1520 (0.9); 2.1421 (1.1); 2.1255 (1.7); 2.1089 (1.4); 2.0972 (1.8); 2.0843 (5.8); 2.0467 (0.6); 1.9563 (1.9); 1.7832 (2.3); 1.7718 (2.0); 1.7617 (2.0); 1.7426 (1.7); 1.7277 (1.7); 1.7006 (2.2); 1.6854 (2.3); 1.6731 (2.6); 1.6612 (2.4); 1.6462 (2.8); 1.6231 (3.1); 1.4530 (1.7); 1.4312 (1.9); 1.4058 (1.5); 1.3817 (1.0); 1.3571 (0.6); 1.3210 (1.1); 1.2972 (2.0); 1.2733 (0.9); 1.0860 (1.2); 1.0662 (2.8); 1.0440 (2.6); 1.0381 (2.6); 1.0251 (1.5); 0.9970 (1.2); 0.9725 (1.8); 0.9480 (0.9); 0.9168 (0.4); 0.8813 (0.4); 0.8630 (0.4); 0.8108 (3.4); 0.7966 (3.3); 0.7784 (1.2); 0.1666 (0.7); 0.1346 (0.5); 0.1067 (2.7); 0.0367 (12.4) I-193: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9644 (5.4); 7.2987 (2.7); 7.1288 (0.6); 7.1025 (1.7); 7.0806 (2.9); 7.0559 (2.5); 7.0283 (1.0); 7.0227 (1.2); 6.9999 (1.5); 6.9778 (0.7); 6.9724 (0.8); 6.9547 (2.6); 6.8572 (0.8); 6.8520 (0.8); 6.8310 (1.5); 6.8092 (0.8); 6.8042 (0.7); 6.7573 (1.4); 6.7317 (1.2); 6.3076 (1.8); 4.2720 (1.2); 4.2469 (1.4); 4.2397 (0.8); 4.1697 (0.4); 4.1460 (0.4); 4.1232 (0.4); 4.1013 (0.5); 3.8964 (0.6); 3.8902 (0.7); 3.8654 (2.0); 3.8323 (1.5); 3.8120 (0.8); 3.4151 (0.6); 3.3836 (0.7); 3.3569 (0.7); 3.0500 (0.7); 3.0350 (0.7); 3.0050 (1.2); 2.9895 (1.1); 2.7991 (0.9); 2.7681 (0.9); 2.7539 (0.9); 2.7232 (0.8); 2.6653 (16.0); 2.3352 (12.8); 2.3128 (0.6); 2.3068 (0.6); 2.3011 (0.5); 2.2876 (0.8); 2.2777 (1.5); 2.2678 (1.3); 2.2521 (1.5); 2.2418 (1.0); 2.2342 (0.6); 2.2281 (0.7); 2.2194 (0.4); 2.1710 (0.3); 2.1531 (0.6); 2.1420 (0.7); 2.1249 (1.2); 2.1078 (0.8); 2.0965 (0.9); 2.0831 (3.5); 2.0579 (0.6); 2.0519 (0.7); 2.0378 (0.7); 2.0307 (1.4); 2.0207 (1.6); 2.0086 (1.9); 2.0025 (2.4); 1.9921 (1.8); 1.9860 (1.4); 1.9635 (0.6); 1.9595 (0.6); 1.9500 (0.5); 1.8559 (0.4); 1.8338 (0.8); 1.8265 (0.9); 1.8173 (0.7); 1.8078 (0.6); 1.7991 (0.4); 1.3201 (0.5); 1.2962 (1.0); 1.2725 (0.4); 1.0892 (0.8); 1.0751 (1.8); 1.0686 (2.0); 1.0550 (1.4); 1.0468 (1.9); 1.0403 (1.9); 1.0268 (1.0); 0.9968 (0.5); 0.9723 (0.9); 0.9478 (0.4); 0.8330 (1.0); 0.8155 (2.4); 0.8019 (2.3); 0.7820 (0.7); 0.1808 (0.4); 0.1757 (0.4); 0.1696 (0.4); 0.1095 (0.3); 0.0373 (3.0) I-194: ¹H-NMR(300.1 MHz, d₆-DMSO): δ = 11.1329 (3.6); 8.2414 (16.0); 7.8090 (5.9); 7.7810 (1.0); 7.7555 (3.2); 7.7300 (5.4); 7.7122 (5.9); 7.6950 (5.4); 7.6717 (7.8); 7.6628 (9.3); 7.6556 (8.7); 7.6439 (7.6); 7.4971 (4.6); 7.4902 (4.2); 7.4690 (3.4); 7.4621 (3.2); 5.2573 (2.2); 5.2397 (2.5); 5.2122 (2.7); 5.1946 (2.2); 3.3274 (2.6); 2.7605 (1.8); 2.7426 (2.1); 2.7304 (0.4); 2.7234 (0.3); 2.7055 (2.9); 2.6878 (2.6); 2.5317 (3.7); 2.5097 (21.9); 2.5040 (28.0); 2.4983 (20.0); 2.4772 (2.6); 2.4317 (2.1); 2.0772 (5.8); −0.0001 (4.3) I-195: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 10.0195 (2.3); 8.2622 (16.0); 7.7817 (1.1); 7.7626 (3.3); 7.7421 (3.8); 7.7200 (10.7); 7.7042 (2.4); 7.6810 (3.8); 7.6575 (9.8); 7.6361 (10.2); 7.4643 (10.8); 7.4431 (8.9); 5.2581 (2.0); 5.2477 (2.2); 5.2269 (2.3); 5.2163 (2.1); 4.0946 (0.6); 3.7996 (2.0); 3.7889 (2.2); 3.7658 (2.7); 3.7552 (2.4); 3.5227 (2.2); 3.4901 (3.4); 3.4574 (1.8); 3.3292 (14.2); 3.1609 (0.3); 2.8905 (1.6); 2.7309 (1.4); 2.6708 (0.4); 2.6670 (0.4); 2.5106 (24.6); 2.5064 (49.0); 2.5020 (65.0); 2.4975 (47.2); 2.4934 (23.2); 2.4441 (0.4); 2.3331 (0.4); 2.3286 (0.4); 2.3240 (0.3); 2.0762 (3.1); 0.0081 (0.3); 0.0000 (8.0) I-196: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.1061 (6.7); 7.2601 (6.1); 7.1886 (3.4); 7.1855 (4.3); 7.1563 (3.3); 6.9955 (2.6); 6.9802 (3.0); 6.9608 (3.2); 6.7899 (1.8); 6.7750 (1.6); 5.9616 (2.0); 4.2837 (1.3); 4.2770 (1.5); 4.2620 (1.5); 4.2553 (1.6); 3.9031 (0.6); 3.8990 (0.7); 3.8949 (0.9); 3.8906 (0.8); 3.8832 (1.0); 3.8795 (0.8); 3.8752 (0.8); 3.8633 (0.4); 3.8174 (1.9); 3.8049 (1.5); 3.7957 (1.8); 3.7832 (1.4); 3.0129 (1.1); 3.0037 (1.2); 2.9853 (1.4); 2.9761 (1.4); 2.7178 (1.5); 2.6975 (1.5); 2.6903 (1.4); 2.6699 (1.2); 2.2848 (16.0); 2.2322 (15.1); 2.1687 (0.9); 1.5633 (5.0); 0.0059 (0.4); −0.0002 (7.1) I-197: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.6129 (2.8); 8.5973 (2.7); 8.5222 (0.8); 8.4418 (0.7); 8.3317 (2.8); 8.3157 (2.8); 8.1354 (6.6); 7.9525 (0.7); 7.2620 (4.7); 6.9665 (2.7); 6.9513 (3.0); 6.9397 (0.5); 6.8818 (3.6); 6.7244 (2.0); 6.7093 (1.7); 5.8554 (2.2); 4.3135 (1.4); 4.3070 (1.5); 4.2918 (1.6); 4.2853 (1.5); 3.9004 (1.0); 3.8948 (1.0); 3.8890 (1.0); 3.8813 (0.8); 3.8300 (2.0); 3.8174 (1.5); 3.8083 (1.8); 3.7957 (1.3); 3.0382 (0.3); 3.0256 (1.3); 3.0160 (1.2); 2.9982 (1.6); 2.9886 (1.4); 2.7155 (1.5); 2.6953 (1.6); 2.6883 (1.4); 2.6680 (1.2); 2.3885 (0.6); 2.2738 (16.0); 2.2587 (0.9); 2.2436 (1.8); 2.1538 (15.4); 2.1422 (2.3); 2.0042 (6.7); 1.5956 (5.1); −0.0002 (5.7) I-198: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.3713 (3.3); 8.3687 (3.6); 8.1234 (3.2); 8.1185 (3.4); 8.1094 (6.3); 7.2615 (5.8); 7.0288 (1.9); 7.0247 (3.2); 7.0211 (2.2); 6.9419 (2.6); 6.9266 (2.9); 6.8872 (3.4); 6.6802 (1.8); 6.6651 (1.6); 6.0662 (2.2); 4.2829 (1.3); 4.2764 (1.4); 4.2613 (1.5); 4.2548 (1.5); 3.8778 (0.6); 3.8686 (0.9); 3.8584 (0.9); 3.8489 (0.7); 3.8086 (1.9); 3.7959 (1.3); 3.7870 (1.7); 3.7743 (1.2); 3.0064 (1.1); 2.9969 (1.2); 2.9790 (1.4); 2.9695 (1.3); 2.6971 (1.4); 2.6772 (1.4); 2.6698 (1.3); 2.6498 (1.2); 2.2634 (16.0); 2.1781 (15.3); 2.0038 (4.3); 1.9860 (0.4); 1.9759 (0.8); 1.9689 (0.9); 1.9591 (1.5); 1.9493 (1.0); 1.9424 (0.8); 1.9322 (0.4); 1.6075 (0.8); 1.1130 (0.8); 1.1013 (2.8); 1.0872 (2.6); 1.0845 (2.7); 1.0751 (0.8); 0.7733 (1.0); 0.7632 (3.2); 0.7526 (3.1); 0.7422 (0.9); −0.0002 (6.7) I-199: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.0368 (10.5); 7.9520 (1.4); 7.5037 (0.4); 7.4984 (2.5); 7.4933 (1.0); 7.4795 (4.4); 7.4777 (4.2); 7.4632 (1.4); 7.4586 (3.7); 7.4528 (0.6); 7.4314 (2.0); 7.4243 (2.0); 7.3185 (1.7); 7.3161 (1.1); 7.3000 (2.8); 7.2840 (0.7); 7.2815 (1.2); 7.2790 (0.7); 7.2519 (4.1); 7.2491 (5.0); 7.2441 (1.3); 7.2302 (4.2); 7.2281 (3.5); 7.2216 (0.4); 7.0504 (2.7); 7.0312 (3.2); 6.9337 (3.2); 6.8020 (1.7); 6.7830 (1.5); 3.7570 (0.6); 3.7389 (1.6); 3.7292 (4.6); 3.7217 (3.3); 3.7100 (1.3); 3.7009 (1.7); 3.6821 (0.4); 3.3374 (62.1); 2.8904 (10.0); 2.8113 (0.4); 2.7942 (1.7); 2.7844 (2.2); 2.7796 (2.1); 2.7679 (1.9); 2.7504 (0.3); 2.7322 (8.6); 2.7314 (8.2); 2.5248 (0.7); 2.5199 (1.0); 2.5113 (13.1); 2.5069 (25.9); 2.5023 (33.6); 2.4977 (24.4); 2.4933 (11.9); 2.2340 (16.0); 2.1914 (14.7); −0.0002 (7.4) I-200: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.0264 (10.8); 7.9518 (1.2); 7.4085 (2.1); 7.4010 (2.0); 7.3687 (1.5); 7.3493 (3.2); 7.3300 (1.9); 7.1216 (2.1); 7.1027 (1.8); 7.0468 (4.7); 7.0445 (4.3); 7.0405 (4.8); 7.0289 (3.4); 7.0199 (1.7); 6.9388 (3.2); 6.8064 (1.7); 6.7874 (1.5); 3.7542 (0.6); 3.7361 (1.6); 3.7260 (4.4); 3.7178 (3.2); 3.7058 (1.2); 3.6969 (1.8); 3.6783 (0.4); 3.3317 (40.4); 2.8901 (9.1); 2.7874 (1.9); 2.7811 (2.2); 2.7722 (2.0); 2.7639 (2.0); 2.7312 (7.8); 2.5244 (0.7); 2.5196 (1.0); 2.5109 (12.6); 2.5065 (25.4); 2.5019 (33.5); 2.4973 (24.5); 2.4928 (12.1); 2.3452 (15.8); 2.3289 (0.4); 2.2333 (16.0); 2.1965 (14.6); −0.0002 (6.0) I-201: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.0473 (10.7); 7.9521 (2.0); 7.5156 (1.4); 7.4960 (3.6); 7.4762 (3.0); 7.4320 (1.7); 7.4290 (3.0); 7.4260 (2.2); 7.4130 (1.1); 7.4097 (2.0); 7.4068 (1.3); 7.3845 (2.8); 7.3790 (5.2); 7.3757 (4.2); 7.3702 (2.3); 7.3388 (1.8); 7.3362 (1.9); 7.3330 (1.6); 7.3303 (1.4); 7.3186 (1.4); 7.3159 (1.4); 7.3127 (1.4); 7.3100 (1.2); 7.0405 (2.8); 7.0213 (3.3); 6.9225 (3.3); 6.7801 (1.7); 6.7622 (1.5); 4.3067 (8.3); 3.7743 (0.4); 3.7558 (2.1); 3.7467 (4.4); 3.7315 (1.0); 3.7224 (1.4); 3.7167 (1.2); 3.7042 (0.8); 3.6954 (0.5); 3.3311 (34.2); 2.8906 (14.9); 2.7890 (3.5); 2.7722 (3.5); 2.7315 (12.4); 2.5248 (0.7); 2.5199 (1.0); 2.5114 (14.0); 2.5069 (28.3); 2.5024 (37.2); 2.4978 (27.3); 2.4933 (13.5); 2.2285 (16.0); 2.1921 (14.8); −0.0002 (8.1) I-202: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 10.0480 (10.1); 8.0739 (11.2); 7.9525 (2.0); 7.8987 (1.3); 7.8957 (2.2); 7.8926 (1.5); 7.8799 (1.8); 7.8767 (2.9); 7.8737 (1.9); 7.7946 (0.4); 7.7893 (2.5); 7.7836 (3.1); 7.7800 (2.6); 7.7526 (2.0); 7.7327 (3.6); 7.7135 (2.2); 7.6308 (1.8); 7.6282 (2.0); 7.6247 (1.8); 7.6221 (1.8); 7.6105 (1.4); 7.6079 (1.4); 7.6044 (1.4); 7.6018 (1.2); 7.4569 (2.1); 7.4489 (2.1); 7.0457 (2.8); 7.0265 (3.2); 6.9114 (3.2); 6.7744 (1.7); 6.7554 (1.5); 3.7486 (6.2); 3.7310 (1.2); 3.7222 (1.1); 3.7126 (0.8); 3.7038 (0.5); 3.3315 (31.6); 2.8910 (14.7); 2.7923 (2.5); 2.7804 (2.1); 2.7753 (2.3); 2.7326 (12.1); 2.7315 (12.4); 2.5252 (0.8); 2.5206 (1.1); 2.5118 (14.1); 2.5073 (28.7); 2.5027 (37.8); 2.4981 (27.6); 2.4936 (13.5); 2.2683 (0.4); 2.2273 (16.0); 2.1696 (14.7); −0.0002 (8.6) I-203: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.0265 (9.6); 7.9520 (0.8); 7.4125 (2.0); 7.4052 (2.0); 7.3939 (1.9); 7.3743 (3.6); 7.3548 (2.3); 7.1564 (2.1); 7.1372 (1.8); 7.0756 (3.2); 7.0524 (4.0); 7.0330 (4.5); 6.9366 (3.2); 6.7952 (1.7); 6.7765 (1.5); 3.7550 (0.6); 3.7369 (1.6); 3.7271 (4.5); 3.7192 (3.2); 3.7066 (1.2); 3.6980 (1.7); 3.6792 (0.4); 3.3299 (26.4); 2.8901 (5.5); 2.7824 (2.3); 2.7723 (2.1); 2.7650 (2.0); 2.7313 (4.8); 2.6775 (1.4); 2.6587 (4.2); 2.6397 (4.3); 2.6207 (1.5); 2.5243 (0.6); 2.5195 (1.0); 2.5108 (12.2); 2.5064 (24.5); 2.5018 (32.2); 2.4973 (23.7); 2.4928 (11.7); 2.2335 (16.0); 2.1907 (14.7); 1.2369 (0.4); 1.2211 (6.6); 1.2022 (13.9); 1.1832 (6.3); −0.0002 (5.3) I-204: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.0331 (6.6); 7.9520 (0.8); 7.4001 (1.2); 7.3915 (2.3); 7.3710 (2.5); 7.3505 (1.4); 7.0489 (1.6); 7.0297 (1.9); 6.9333 (1.8); 6.8935 (0.8); 6.8917 (1.0); 6.8875 (1.1); 6.8857 (1.2); 6.8728 (0.8); 6.8711 (0.8); 6.8667 (1.1); 6.8649 (1.1); 6.8418 (1.3); 6.8363 (2.6); 6.8306 (1.5); 6.8213 (1.3); 6.8194 (1.4); 6.8159 (0.9); 6.8139 (0.9); 6.8015 (1.6); 6.7997 (1.4); 6.7958 (1.1); 6.7938 (1.1); 6.7890 (0.9); 3.7654 (16.0); 3.7419 (1.0); 3.7302 (1.6); 3.7171 (1.8); 3.7100 (0.9); 3.6966 (0.9); 3.6908 (0.6); 3.3311 (21.3); 2.8903 (5.6); 2.7866 (1.1); 2.7804 (1.3); 2.7715 (1.1); 2.7638 (1.2); 2.7322 (4.7); 2.7310 (4.8); 2.5244 (0.4); 2.5197 (0.6); 2.5111 (7.1); 2.5066 (14.4); 2.5020 (19.0); 2.4974 (14.0); 2.4929 (6.8); 2.2330 (9.3); 2.1933 (8.5); −0.0002 (4.4) I-205: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.0824 (9.6); 7.9525 (1.5); 7.4187 (2.1); 7.4107 (2.0); 7.2695 (0.5); 7.2649 (0.6); 7.2527 (1.2); 7.2467 (1.5); 7.2389 (1.0); 7.2303 (1.5); 7.2154 (1.8); 7.2103 (1.3); 7.2010 (5.9); 7.1932 (1.2); 7.1845 (2.4); 7.1641 (0.6); 7.0566 (2.7); 7.0374 (3.2); 6.9327 (3.2); 6.8270 (1.7); 6.8094 (1.5); 3.7812 (0.4); 3.7628 (2.0); 3.7536 (4.3); 3.7383 (1.0); 3.7290 (1.4); 3.7232 (1.2); 3.7108 (0.8); 3.7021 (0.5); 3.3305 (28.1); 2.8906 (10.9); 2.8474 (0.3); 2.8297 (0.4); 2.8124 (1.7); 2.7995 (2.5); 2.7834 (1.8); 2.7662 (0.4); 2.7498 (0.3); 2.7319 (9.3); 2.5248 (0.6); 2.5199 (1.0); 2.5114 (12.4); 2.5070 (24.8); 2.5025 (32.6); 2.4979 (23.9); 2.4935 (11.8); 2.3001 (9.3); 2.2961 (9.4); 2.2416 (16.0); 2.1921 (14.6); −0.0002 (5.8) I-206: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.0006 (7.9); 7.9492 (4.5); 7.9478 (4.4); 7.5006 (4.2); 7.4990 (4.1); 7.4429 (1.3); 7.4348 (1.3); 7.0869 (1.6); 7.0678 (2.0); 6.9731 (2.0); 6.8823 (1.1); 6.8637 (0.9); 4.5285 (0.4); 4.5118 (1.1); 4.4952 (1.5); 4.4786 (1.1); 4.4619 (0.4); 3.7362 (3.5); 3.7231 (0.6); 3.7136 (0.8); 3.7077 (0.6); 3.7043 (0.6); 3.6964 (0.5); 3.3280 (34.5); 2.8907 (3.6); 2.8391 (0.3); 2.8214 (0.9); 2.8049 (1.0); 2.7984 (1.1); 2.7805 (1.0); 2.7321 (3.0); 2.7308 (3.0); 2.5244 (0.7); 2.5196 (1.1); 2.5109 (13.7); 2.5064 (27.6); 2.5019 (36.0); 2.4973 (26.3); 2.4928 (12.8); 2.2561 (10.0); 2.2176 (9.1); 1.4407 (16.0); 1.4240 (15.8); −0.0002 (7.4) I-207: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.1276 (10.9); 7.9532 (1.4); 7.4903 (0.4); 7.4864 (0.5); 7.4688 (1.1); 7.4651 (1.1); 7.4602 (0.8); 7.4499 (2.7); 7.4477 (2.7); 7.4428 (2.8); 7.4257 (0.6); 7.4218 (0.6); 7.3744 (0.5); 7.3696 (0.5); 7.3596 (0.5); 7.3535 (1.1); 7.3486 (1.1); 7.3386 (1.0); 7.3343 (1.2); 7.3275 (0.6); 7.3174 (0.6); 7.3138 (0.6); 7.2930 (0.8); 7.2890 (1.3); 7.2856 (0.9); 7.2726 (1.5); 7.2686 (1.3); 7.2518 (0.8); 7.0621 (2.7); 7.0429 (3.2); 6.9302 (3.2); 6.8394 (1.7); 6.8204 (1.5); 3.7606 (6.4); 3.7425 (1.2); 3.7337 (1.0); 3.7240 (0.7); 3.7153 (0.5); 3.3319 (32.7); 2.8914 (10.8); 2.8554 (0.4); 2.8376 (0.5); 2.8207 (1.5); 2.8045 (3.1); 2.7874 (1.8); 2.7698 (0.4); 2.7536 (0.4); 2.7331 (8.6); 2.7322 (9.0); 2.5257 (0.7); 2.5210 (1.1); 2.5122 (12.6); 2.5078 (25.3); 2.5032 (33.1); 2.4986 (24.2); 2.4941 (11.8); 2.2429 (16.0); 2.1931 (14.6); −0.0002 (6.6) I-208: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 11.2170 (2.0); 8.3156 (0.3); 7.9940 (10.5); 7.9519 (0.4); 7.4546 (3.5); 7.4481 (2.4); 7.4404 (2.3); 7.4329 (3.9); 7.4220 (3.6); 7.4151 (2.3); 7.3697 (3.6); 7.3641 (3.7); 7.0650 (2.8); 7.0458 (3.2); 6.9717 (2.4); 6.9660 (2.3); 6.9500 (2.3); 6.9441 (2.5); 6.9346 (3.3); 6.8085 (1.7); 6.7896 (1.5); 6.4575 (1.9); 6.4523 (2.8); 6.4472 (1.9); 3.7882 (0.3); 3.7768 (1.0); 3.7584 (1.7); 3.7468 (1.8); 3.7335 (1.6); 3.7253 (2.9); 3.7107 (1.2); 3.7046 (1.7); 3.3360 (50.2); 2.8891 (3.1); 2.8419 (0.3); 2.8253 (0.4); 2.8077 (1.6); 2.7936 (2.6); 2.7782 (1.7); 2.7609 (0.4); 2.7316 (2.6); 2.7307 (2.6); 2.5242 (0.8); 2.5195 (1.2); 2.5108 (14.7); 2.5064 (29.2); 2.5018 (38.1); 2.4972 (27.8); 2.4927 (13.6); 2.2397 (16.0); 2.1770 (14.6); −0.0002 (7.5) I-209: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.0448 (10.4); 7.9522 (1.6); 7.3686 (2.0); 7.3613 (2.0); 7.2510 (1.1); 7.2321 (2.9); 7.2129 (2.4); 7.1842 (2.9); 7.1667 (1.5); 7.0486 (2.8); 7.0294 (3.2); 7.0069 (2.6); 6.9875 (2.2); 6.9326 (3.2); 6.8133 (1.7); 6.7943 (1.5); 3.7669 (0.8); 3.7490 (1.6); 3.7374 (4.0); 3.7278 (3.3); 3.7195 (1.4); 3.7077 (1.6); 3.7007 (1.0); 3.6916 (0.4); 3.3306 (31.7); 2.9548 (1.8); 2.9364 (3.5); 2.9178 (1.9); 2.8904 (12.2); 2.8148 (0.3); 2.7972 (1.6); 2.7885 (2.2); 2.7823 (2.0); 2.7720 (1.9); 2.7319 (10.0); 2.7314 (10.0); 2.5975 (1.1); 2.5881 (1.1); 2.5790 (2.2); 2.5698 (2.1); 2.5603 (1.2); 2.5517 (1.2); 2.5287 (0.4); 2.5247 (0.8); 2.5198 (1.1); 2.5111 (13.0); 2.5067 (26.1); 2.5021 (34.3); 2.4975 (25.0); 2.4930 (12.3); 2.2342 (16.0); 2.1938 (14.6); 2.0208 (0.6); 2.0024 (2.2); 1.9839 (3.1); 1.9652 (2.0); 1.9462 (0.5); −0.0002 (6.9) I-210: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.0074 (10.5); 7.9519 (1.7); 7.3966 (2.1); 7.3890 (2.1); 7.2947 (2.5); 7.2744 (2.8); 7.0710 (2.9); 7.0662 (3.1); 7.0481 (2.7); 7.0290 (3.2); 6.9804 (2.0); 6.9747 (1.8); 6.9601 (1.8); 6.9545 (1.7); 6.9401 (3.3); 6.8091 (1.7); 6.7907 (1.5); 3.7603 (0.8); 3.7421 (1.7); 3.7305 (3.1); 3.7196 (3.0); 3.7040 (1.2); 3.6971 (1.7); 3.6859 (0.8); 3.6770 (0.4); 3.3299 (34.2); 2.9003 (3.1); 2.8902 (14.4); 2.8827 (5.8); 2.8639 (3.1); 2.7874 (2.1); 2.7820 (2.2); 2.7719 (2.2); 2.7644 (2.0); 2.7475 (0.3); 2.7315 (10.5); 2.5242 (0.8); 2.5193 (1.2); 2.5108 (14.2); 2.5064 (27.9); 2.5018 (36.1); 2.4972 (26.3); 2.4928 (12.8); 2.2348 (16.0); 2.1965 (14.6); 2.1091 (0.7); 2.0906 (2.4); 2.0720 (3.4); 2.0538 (2.3); 2.0353 (0.6); −0.0002 (6.9) I-211: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.2211 (2.9); 8.2148 (3.1); 8.0498 (10.1); 7.9522 (2.0); 7.5363 (2.7); 7.5303 (2.8); 7.4099 (2.0); 7.4021 (2.0); 7.0500 (2.7); 7.0308 (3.1); 6.9279 (3.1); 6.7980 (1.7); 6.7800 (1.4); 3.7805 (0.4); 3.7622 (1.9); 3.7526 (4.4); 3.7291 (1.3); 3.7235 (1.3); 3.7134 (0.8); 3.7044 (0.5); 3.3397 (13.4); 2.9659 (1.8); 2.9488 (4.9); 2.9307 (5.5); 2.9120 (2.4); 2.8910 (14.5); 2.8169 (0.3); 2.7951 (2.4); 2.7832 (2.1); 2.7776 (2.2); 2.7323 (12.1); 2.7314 (11.7); 2.5248 (0.8); 2.5201 (1.2); 2.5115 (14.0); 2.5070 (28.4); 2.5024 (37.4); 2.4978 (27.4); 2.4934 (13.5); 2.2620 (0.4); 2.2349 (16.0); 2.1900 (14.3); 2.1601 (2.4); 2.1411 (3.2); 2.1225 (2.2); 2.1035 (0.6); −0.0002 (7.3) I-212: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 7.9916 (11.5); 7.3976 (2.1); 7.3898 (2.1); 7.1111 (2.8); 7.1050 (3.0); 7.0593 (2.7); 7.0401 (3.2); 6.9477 (4.5); 6.9328 (2.2); 6.9264 (2.1); 6.8286 (1.8); 6.8188 (5.0); 6.8128 (1.7); 6.7975 (3.6); 4.6007 (2.6); 4.5789 (5.6); 4.5571 (2.8); 3.7697 (0.7); 3.7515 (1.8); 3.7406 (3.5); 3.7310 (3.1); 3.7219 (1.0); 3.7113 (1.6); 3.7054 (1.5); 3.6939 (0.8); 3.6849 (0.5); 3.3317 (37.3); 3.2348 (1.9); 3.2132 (3.7); 3.1915 (1.8); 2.8903 (1.3); 2.7971 (2.0); 2.7908 (2.2); 2.7814 (2.1); 2.7735 (1.9); 2.7319 (1.1); 2.5243 (0.7); 2.5196 (1.0); 2.5109 (12.6); 2.5065 (25.4); 2.5019 (33.3); 2.4973 (24.3); 2.4928 (11.8); 2.2400 (16.0); 2.2038 (14.7); −0.0002 (6.8) I-213: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.0603 (7.4); 7.9523 (1.2); 7.9360 (0.9); 7.9327 (1.3); 7.9297 (1.0); 7.9168 (1.1); 7.9132 (1.5); 7.9105 (1.1); 7.8173 (1.6); 7.8123 (2.2); 7.8077 (1.6); 7.6678 (1.2); 7.6479 (2.5); 7.6283 (1.5); 7.5541 (1.2); 7.5517 (1.3); 7.5482 (1.2); 7.5458 (1.2); 7.5339 (0.9); 7.5315 (0.9); 7.5279 (0.9); 7.5255 (0.8); 7.4515 (1.4); 7.4436 (1.3); 7.0477 (1.8); 7.0285 (2.0); 6.9130 (2.0); 6.7775 (1.1); 6.7589 (1.0); 3.7611 (1.2); 3.7517 (2.9); 3.7401 (0.8); 3.7272 (0.8); 3.7225 (0.9); 3.7122 (0.5); 3.3317 (27.3); 2.8908 (8.4); 2.7929 (1.7); 2.7791 (1.5); 2.7755 (1.5); 2.7324 (6.9); 2.7313 (7.1); 2.6060 (16.0); 2.5250 (0.6); 2.5201 (0.8); 2.5115 (9.5); 2.5070 (18.9); 2.5025 (24.6); 2.4978 (17.9); 2.4933 (8.7); 2.2283 (10.2); 2.1703 (9.4); −0.0002 (5.0) I-214: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.0246 (11.2); 7.9522 (0.5); 7.4096 (2.1); 7.4020 (2.1); 7.3878 (1.4); 7.3687 (2.7); 7.3673 (2.8); 7.3482 (1.7); 7.1339 (2.3); 7.1145 (1.9); 7.0534 (8.3); 7.0339 (4.8); 6.9353 (3.2); 6.7911 (1.7); 6.7732 (1.5); 3.7551 (0.6); 3.7370 (1.7); 3.7274 (4.4); 3.7200 (3.3); 3.7063 (1.2); 3.6980 (1.6); 3.6876 (0.8); 3.6787 (0.5); 3.3301 (32.0); 2.8903 (3.9); 2.7822 (2.3); 2.7714 (2.1); 2.7648 (2.1); 2.7322 (3.4); 2.7312 (3.4); 2.6117 (2.4); 2.5933 (3.5); 2.5738 (2.6); 2.5245 (0.7); 2.5197 (1.0); 2.5110 (12.6); 2.5066 (25.5); 2.5020 (33.4); 2.4974 (24.4); 2.4929 (12.0); 2.2315 (16.0); 2.1900 (14.7); 1.6579 (0.4); 1.6394 (1.7); 1.6207 (2.9); 1.6017 (2.9); 1.5832 (1.7); 1.5649 (0.4); 0.9287 (6.3); 0.9105 (12.9); 0.8921 (5.7); −0.0002 (7.1) I-215: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.0036 (3.9); 7.9519 (0.6); 7.3949 (0.8); 7.3877 (0.8); 7.2556 (0.7); 7.2352 (1.4); 7.2148 (0.9); 7.0527 (1.0); 7.0335 (1.2); 6.9399 (1.2); 6.8189 (0.6); 6.7998 (0.6); 6.6436 (0.6); 6.6377 (0.6); 6.6227 (0.5); 6.6173 (0.6); 6.5457 (0.8); 6.5400 (1.4); 6.5343 (0.8); 6.4784 (0.7); 6.4737 (0.6); 6.4587 (0.6); 6.4543 (0.6); 3.7603 (0.4); 3.7418 (0.6); 3.7302 (0.6); 3.7051 (1.1); 3.6920 (0.5); 3.6846 (0.6); 3.3289 (28.5); 2.9018 (16.0); 2.8905 (4.2); 2.7770 (0.9); 2.7660 (0.8); 2.7609 (0.8); 2.7312 (3.5); 2.5241 (0.5); 2.5193 (0.8); 2.5107 (9.8); 2.5063 (19.7); 2.5018 (25.8); 2.4972 (18.9); 2.4928 (9.4); 2.2351 (6.0); 2.1947 (5.5); −0.0002 (4.8) I-216: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.0306 (11.3); 7.9521 (1.1); 7.3869 (2.2); 7.3794 (2.2); 7.3736 (2.4); 7.3532 (3.9); 7.3328 (2.2); 7.0455 (2.8); 7.0263 (3.2); 6.9329 (3.2); 6.8705 (1.6); 6.8665 (1.8); 6.8648 (1.8); 6.8500 (1.4); 6.8456 (1.9); 6.8441 (1.8); 6.8187 (2.0); 6.8133 (4.2); 6.8051 (4.3); 6.8032 (4.3); 6.8000 (3.0); 6.7848 (3.3); 6.7834 (3.4); 6.7798 (2.9); 4.0477 (1.6); 4.0303 (5.3); 4.0128 (5.4); 3.9954 (1.7); 3.7596 (0.9); 3.7416 (1.7); 3.7301 (2.6); 3.7254 (2.3); 3.7160 (3.2); 3.7078 (1.4); 3.6959 (1.7); 3.6888 (1.1); 3.6807 (0.4); 3.3307 (38.4); 2.8904 (8.2); 2.7797 (2.4); 2.7676 (2.2); 2.7628 (2.2); 2.7320 (6.9); 2.5245 (0.7); 2.5197 (1.1); 2.5110 (13.6); 2.5066 (27.4); 2.5021 (35.7); 2.4975 (26.0); 2.4930 (12.7); 2.2311 (16.0); 2.1930 (14.7); 1.3440 (5.9); 1.3266 (12.4); 1.3092 (5.7); −0.0002 (7.1) I-217: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.0319 (11.6); 7.9519 (0.7); 7.4689 (1.8); 7.4493 (3.8); 7.4297 (4.0); 7.2481 (2.2); 7.2290 (1.9); 7.2092 (2.0); 7.2044 (3.1); 7.1715 (1.8); 7.1673 (1.4); 7.1515 (1.4); 7.1472 (1.3); 7.0501 (2.8); 7.0310 (3.2); 6.9354 (3.2); 6.8018 (1.7); 6.7844 (1.4); 4.4582 (11.5); 3.7587 (0.4); 3.7405 (2.0); 3.7310 (4.4); 3.7178 (1.1); 3.7073 (1.3); 3.7013 (1.2); 3.6904 (0.8); 3.6817 (0.5); 3.3313 (38.8); 3.3211 (34.2); 2.8902 (5.2); 2.7862 (2.4); 2.7741 (2.1); 2.7688 (2.2); 2.7321 (4.3); 2.7310 (4.2); 2.5244 (0.7); 2.5196 (1.1); 2.5110 (12.6); 2.5065 (25.7); 2.5019 (34.0); 2.4973 (24.8); 2.4927 (12.1); 2.2331 (16.0); 2.1917 (14.6); −0.0002 (7.2) I-218: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.2138 (1.0); 8.2082 (2.0); 8.2054 (1.1); 8.2014 (2.3); 8.1983 (2.5); 8.1952 (4.1); 8.1933 (6.3); 8.1885 (6.6); 8.1787 (0.4); 8.0908 (12.9); 7.9527 (2.1); 7.8229 (0.5); 7.8200 (0.4); 7.8026 (3.4); 7.7965 (3.4); 7.7912 (4.1); 7.7877 (3.7); 7.7846 (6.3); 7.7755 (0.6); 7.4419 (2.0); 7.4338 (2.0); 7.0467 (2.8); 7.0275 (3.2); 6.8947 (3.2); 6.7646 (1.7); 6.7457 (1.5); 3.7702 (6.3); 3.7551 (1.2); 3.7465 (1.0); 3.7370 (0.7); 3.7284 (0.5); 3.3324 (44.2); 2.8915 (15.4); 2.8001 (3.0); 2.7835 (2.9); 2.7331 (12.8); 2.7318 (13.0); 2.5256 (0.8); 2.5209 (1.2); 2.5122 (14.0); 2.5077 (28.2); 2.5031 (37.0); 2.4984 (26.8); 2.4939 (12.8); 2.2239 (16.0); 2.1581 (14.7); −0.0002 (8.4) I-219: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 10.2376 (7.3); 8.1356 (10.4); 7.9526 (1.9); 7.8429 (0.8); 7.8389 (1.0); 7.8276 (1.0); 7.8237 (1.8); 7.8195 (1.2); 7.8085 (1.0); 7.8044 (1.0); 7.7818 (0.8); 7.7778 (0.9); 7.7620 (1.7); 7.7585 (1.6); 7.7429 (1.1); 7.7388 (0.9); 7.5267 (1.5); 7.5069 (2.6); 7.4870 (1.2); 7.4632 (2.0); 7.4551 (2.0); 7.0633 (2.7); 7.0441 (3.1); 6.9232 (3.2); 6.8321 (1.7); 6.8131 (1.4); 3.7680 (6.2); 3.7512 (1.2); 3.7421 (1.1); 3.7329 (0.8); 3.7241 (0.5); 3.3574 (0.3); 3.3328 (72.2); 2.8913 (13.7); 2.8607 (0.4); 2.8430 (0.5); 2.8260 (1.4); 2.8101 (3.0); 2.7933 (1.8); 2.7760 (0.4); 2.7592 (0.3); 2.7324 (11.4); 2.6717 (0.4); 2.5252 (1.2); 2.5205 (1.7); 2.5118 (20.4); 2.5073 (41.3); 2.5028 (54.4); 2.4982 (40.0); 2.4937 (19.7); 2.3297 (0.4); 2.2431 (16.0); 2.1804 (14.4); 1.2394 (0.6); −0.0002 (10.0) I-220: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.0828 (11.1); 7.9528 (1.0); 7.4192 (2.0); 7.4110 (2.0); 7.2919 (0.5); 7.2840 (0.7); 7.2763 (1.2); 7.2678 (1.6); 7.2616 (0.9); 7.2523 (1.4); 7.2465 (0.9); 7.2322 (3.7); 7.2273 (3.6); 7.2231 (2.6); 7.2133 (2.9); 7.0584 (2.8); 7.0392 (3.2); 6.9299 (3.2); 6.8201 (1.7); 6.8018 (1.5); 3.7815 (0.4); 3.7535 (4.8); 3.7386 (1.0); 3.7282 (1.3); 3.7195 (1.0); 3.7111 (0.8); 3.7022 (0.5); 3.3326 (39.5); 2.8908 (7.5); 2.8479 (0.4); 2.8304 (0.4); 2.8132 (1.7); 2.8009 (2.4); 2.7845 (1.8); 2.7674 (0.4); 2.7506 (0.3); 2.7326 (6.2); 2.7317 (6.2); 2.7119 (1.1); 2.6930 (3.3); 2.6742 (3.5); 2.6553 (1.2); 2.5252 (0.7); 2.5204 (1.0); 2.5118 (12.7); 2.5073 (25.7); 2.5027 (33.8); 2.4981 (24.7); 2.4936 (12.1); 2.2417 (16.0); 2.1871 (14.6); 1.2274 (6.1); 1.2086 (13.1); 1.1897 (5.8); −0.0002 (6.8) I-221: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.0358 (12.4); 7.9518 (1.4); 7.4278 (2.0); 7.4078 (4.4); 7.3879 (4.7); 7.3812 (2.2); 7.2042 (1.6); 7.2022 (2.0); 7.2000 (2.1); 7.1980 (2.0); 7.1845 (1.4); 7.1824 (1.6); 7.1802 (1.9); 7.1782 (1.7); 7.1533 (2.7); 7.1483 (4.2); 7.1434 (2.4); 7.0447 (2.8); 7.0262 (4.8); 7.0084 (1.7); 7.0064 (1.7); 7.0028 (1.7); 7.0008 (1.6); 6.9315 (3.2); 6.7958 (1.7); 6.7783 (1.5); 3.7715 (0.8); 3.7532 (1.7); 3.7417 (2.9); 3.7296 (3.0); 3.7160 (1.2); 3.7081 (1.9); 3.6886 (0.5); 3.3309 (40.9); 2.8902 (10.6); 2.7854 (3.4); 2.7687 (3.1); 2.7319 (8.5); 2.7310 (8.8); 2.5243 (0.7); 2.5196 (1.2); 2.5109 (13.2); 2.5065 (26.5); 2.5019 (34.6); 2.4973 (25.4); 2.4928 (12.8); 2.4858 (28.2); 2.2310 (16.0); 2.1955 (14.7); −0.0002 (6.7) I-222: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.0384 (12.8); 7.4652 (2.7); 7.4442 (3.0); 7.4433 (3.0); 7.3792 (4.2); 7.3731 (4.8); 7.3670 (2.4); 7.3588 (2.1); 7.1791 (2.3); 7.1731 (2.2); 7.1584 (2.1); 7.1524 (2.0); 7.0430 (2.7); 7.0238 (3.2); 6.9261 (3.2); 6.7913 (1.7); 6.7726 (1.5); 3.7755 (0.5); 3.7574 (1.8); 3.7484 (4.2); 3.7428 (3.7); 3.7335 (1.1); 3.7223 (1.4); 3.7164 (1.3); 3.7057 (0.8); 3.6968 (0.5); 3.3295 (28.9); 2.8906 (1.4); 2.7879 (3.4); 2.7710 (3.2); 2.7324 (1.2); 2.7313 (1.2); 2.5248 (0.8); 2.5201 (1.0); 2.5113 (12.5); 2.5068 (25.4); 2.5022 (33.4); 2.4976 (24.6); 2.4931 (12.1); 2.3677 (16.0); 2.2301 (15.8); 2.1921 (14.5); −0.0002 (7.4) I-223: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.0803 (10.0); 8.0432 (3.0); 8.0208 (3.3); 8.0060 (1.8); 7.9873 (1.9); 7.9841 (1.8); 7.9529 (2.1); 7.9269 (1.8); 7.9080 (2.0); 7.7449 (3.2); 7.7392 (3.4); 7.5925 (0.6); 7.5889 (0.8); 7.5753 (2.0); 7.5717 (1.8); 7.5574 (3.0); 7.5537 (3.0); 7.5393 (1.8); 7.5357 (1.9); 7.5221 (0.8); 7.5185 (0.6); 7.4777 (2.1); 7.4718 (2.1); 7.4493 (2.4); 7.4434 (2.3); 7.4271 (2.2); 7.4211 (2.2); 7.0478 (2.8); 7.0286 (3.2); 6.9102 (3.3); 6.7676 (1.8); 6.7499 (1.6); 3.7658 (1.0); 3.7472 (1.8); 3.7356 (3.4); 3.7306 (3.1); 3.7218 (2.8); 3.7019 (1.4); 3.3353 (43.9); 2.8900 (14.6); 2.8358 (0.4); 2.8191 (0.4); 2.8017 (1.2); 2.7838 (2.5); 2.7676 (1.6); 2.7502 (0.4); 2.7323 (12.6); 2.5250 (0.8); 2.5117 (13.2); 2.5073 (26.5); 2.5028 (34.9); 2.4982 (25.9); 2.4939 (13.0); 2.2270 (16.0); 2.1406 (14.8); 0.9123 (0.4); −0.0002 (6.4) I-224: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.8912 (4.7); 8.8845 (4.8); 8.2638 (3.2); 8.2574 (3.2); 8.1237 (12.4); 8.0984 (2.4); 8.0280 (1.9); 8.0092 (2.1); 8.0071 (2.1); 7.8224 (1.2); 7.8188 (1.3); 7.8051 (1.7); 7.8014 (2.4); 7.7977 (1.2); 7.7840 (1.5); 7.7804 (1.4); 7.7069 (1.5); 7.7041 (1.5); 7.6867 (2.4); 7.6840 (1.6); 7.6693 (1.1); 7.6665 (1.0); 7.4969 (2.0); 7.4903 (1.9); 7.0545 (2.7); 7.0353 (3.1); 6.8868 (3.1); 6.7458 (1.6); 6.7288 (1.5); 3.7921 (0.5); 3.7661 (6.2); 3.7421 (0.9); 3.3314 (265.9); 3.2973 (0.3); 2.8909 (1.7); 2.8520 (0.3); 2.8346 (0.4); 2.8183 (1.1); 2.8015 (2.4); 2.7860 (1.6); 2.7311 (1.4); 2.6802 (0.4); 2.6759 (0.7); 2.6713 (1.0); 2.6668 (0.8); 2.6623 (0.4); 2.5249 (3.1); 2.5201 (4.6); 2.5114 (59.7); 2.5070 (121.3); 2.5024 (159.8); 2.4978 (117.0); 2.4933 (57.5); 2.3381 (0.3); 2.3337 (0.7); 2.3292 (1.0); 2.3247 (0.7); 2.3201 (0.4); 2.2294 (16.0); 2.1116 (14.6); 1.2398 (1.1); 0.0080 (1.0); −0.0002 (33.0); −0.0085 (1.1) I-225: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.0839 (12.1); 7.4439 (1.3); 7.4386 (2.0); 7.4335 (1.4); 7.4221 (1.3); 7.4171 (2.0); 7.4118 (1.3); 7.3355 (2.1); 7.3276 (2.1); 7.3131 (1.7); 7.3082 (3.3); 7.3056 (3.3); 7.3011 (1.9); 7.2798 (1.6); 7.2743 (2.2); 7.2689 (1.1); 7.2557 (1.5); 7.2503 (2.3); 7.2448 (1.1); 7.0395 (2.8); 7.0203 (3.2); 6.9201 (3.3); 6.7871 (1.8); 6.7686 (1.5); 3.7514 (6.3); 3.7373 (1.3); 3.7284 (1.2); 3.7187 (0.8); 3.7099 (0.5); 3.3317 (39.5); 2.8910 (1.2); 2.7876 (3.4); 2.7707 (3.3); 2.7327 (1.0); 2.7316 (1.0); 2.5251 (0.7); 2.5204 (1.0); 2.5116 (12.2); 2.5072 (24.6); 2.5026 (32.2); 2.4980 (23.7); 2.4935 (11.7); 2.2265 (16.0); 2.1943 (14.7); −0.0002 (6.8) I-226: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.0558 (9.3); 7.9520 (1.7); 7.5986 (1.9); 7.5915 (2.1); 7.5827 (2.1); 7.5754 (3.7); 7.5524 (3.9); 7.5298 (2.1); 7.3616 (2.3); 7.3531 (3.4); 7.3458 (1.8); 7.3433 (1.9); 7.3358 (1.3); 7.3304 (1.2); 7.3207 (1.3); 7.3132 (1.0); 7.0465 (2.7); 7.0273 (3.2); 6.9189 (3.5); 6.7885 (1.9); 6.7693 (1.6); 3.7600 (6.3); 3.7488 (1.3); 3.7385 (1.3); 3.7306 (1.2); 3.7217 (0.8); 3.7130 (0.5); 3.3339 (44.9); 2.8911 (10.6); 2.7958 (3.7); 2.7789 (3.6); 2.7318 (9.7); 2.5073 (23.3); 2.5029 (30.8); 2.4984 (23.5); 2.2299 (16.0); 2.1910 (14.8); −0.0002 (4.1) I-227: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.1186 (9.4); 7.9532 (1.6); 7.9091 (0.7); 7.8901 (0.8); 7.8829 (1.3); 7.8642 (1.3); 7.8567 (0.8); 7.8380 (0.6); 7.6990 (0.7); 7.6796 (1.2); 7.6720 (0.8); 7.6605 (0.8); 7.6529 (1.2); 7.6337 (0.6); 7.3903 (2.0); 7.3824 (2.0); 7.0617 (2.6); 7.0426 (3.2); 6.9212 (3.2); 6.8429 (1.7); 6.8234 (1.5); 3.7696 (6.4); 3.7569 (1.3); 3.7477 (1.2); 3.7382 (0.8); 3.7292 (0.6); 3.3311 (25.3); 2.8917 (11.0); 2.8566 (0.4); 2.8383 (0.5); 2.8218 (1.4); 2.8065 (2.8); 2.7903 (1.8); 2.7725 (0.4); 2.7328 (9.4); 2.5256 (0.7); 2.5121 (12.8); 2.5077 (25.2); 2.5032 (32.6); 2.4986 (23.9); 2.4943 (11.8); 2.2696 (0.6); 2.2381 (16.0); 2.1938 (14.2); −0.0002 (6.2) I-228: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.0248 (10.7); 7.9519 (1.2); 7.4088 (3.6); 7.4035 (2.2); 7.3890 (3.9); 7.3694 (2.5); 7.1710 (2.1); 7.1518 (1.8); 7.0952 (1.9); 7.0908 (3.3); 7.0519 (4.5); 7.0326 (4.7); 6.9344 (3.2); 6.7839 (1.7); 6.7665 (1.5); 3.7626 (0.7); 3.7445 (1.7); 3.7337 (3.9); 3.7246 (3.1); 3.7091 (1.2); 3.7017 (1.6); 3.6905 (0.8); 3.6818 (0.5); 3.5848 (1.0); 3.5625 (1.5); 3.5406 (1.0); 3.5188 (0.3); 3.3332 (51.8); 2.8903 (9.4); 2.7852 (2.8); 2.7694 (2.4); 2.7313 (7.8); 2.5246 (0.8); 2.5199 (1.1); 2.5112 (13.4); 2.5067 (27.2); 2.5021 (36.0); 2.4975 (26.4); 2.4930 (13.0); 2.3429 (0.7); 2.3363 (0.9); 2.3295 (0.7); 2.3225 (1.4); 2.3155 (2.4); 2.3087 (1.4); 2.3016 (1.2); 2.2947 (2.4); 2.2884 (1.8); 2.2803 (0.7); 2.2742 (1.1); 2.2690 (1.0); 2.2332 (16.0); 2.1878 (14.7); 2.1503 (0.4); 2.1474 (0.4); 2.1437 (0.4); 2.1248 (1.4); 2.1187 (1.0); 2.1011 (2.2); 2.0957 (1.8); 2.0794 (1.5); 2.0727 (1.7); 2.0569 (0.5); 2.0529 (0.5); 2.0506 (0.6); 2.0326 (0.5); 2.0141 (0.9); 2.0087 (0.7); 1.9941 (0.5); 1.9893 (1.4); 1.9819 (0.4); 1.9726 (0.3); 1.9644 (1.3); 1.9458 (0.5); 1.9401 (0.6); 1.8499 (0.4); 1.8444 (0.6); 1.8242 (1.1); 1.8224 (1.1); 1.8178 (0.8); 1.8062 (0.5); 1.8027 (0.8); 1.7991 (0.8); 1.7962 (0.9); −0.0002 (7.1) I-229: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.0397 (10.3); 7.9519 (1.4); 7.4946 (1.7); 7.4750 (3.7); 7.4552 (2.6); 7.4273 (2.1); 7.4199 (2.0); 7.3456 (2.2); 7.3261 (1.7); 7.2979 (2.2); 7.2930 (3.4); 7.2887 (2.1); 7.1581 (1.7); 7.1542 (1.6); 7.1524 (1.5); 7.1399 (1.4); 7.1379 (1.5); 7.1341 (1.5); 7.0508 (2.7); 7.0316 (3.2); 6.9303 (3.2); 6.7818 (1.7); 6.7642 (1.5); 4.9745 (2.6); 4.9727 (2.7); 4.9598 (3.1); 4.9578 (3.2); 4.9538 (3.2); 4.9518 (3.1); 4.9390 (3.1); 4.9371 (3.1); 4.6345 (3.9); 4.6186 (6.2); 4.6030 (4.0); 4.3343 (0.5); 4.3139 (1.0); 4.2965 (1.7); 4.2792 (0.9); 4.2764 (0.9); 4.2588 (0.3); 3.7609 (0.6); 3.7428 (1.6); 3.7331 (4.4); 3.7255 (3.2); 3.7117 (1.2); 3.7035 (1.6); 3.6931 (0.8); 3.6842 (0.4); 3.3333 (95.9); 2.8905 (11.0); 2.7836 (2.4); 2.7713 (2.2); 2.7660 (2.1); 2.7311 (9.2); 2.6710 (0.4); 2.5246 (1.1); 2.5198 (1.6); 2.5111 (21.4); 2.5067 (43.3); 2.5021 (56.9); 2.4975 (41.7); 2.4930 (20.6); 2.3290 (0.4); 2.2314 (16.0); 2.1819 (14.7); 1.2391 (0.4); −0.0002 (10.0); −0.0085 (0.4) I-230: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.0576 (9.9); 7.9730 (3.8); 7.9516 (6.1); 7.8960 (3.5); 7.8907 (3.5); 7.7958 (4.7); 7.7822 (5.2); 7.5166 (3.5); 7.5029 (3.2); 7.4408 (2.2); 7.4341 (2.1); 7.3079 (2.7); 7.3024 (2.6); 7.2863 (2.6); 7.2809 (2.5); 7.0488 (2.8); 7.0296 (3.2); 6.9165 (3.3); 6.7702 (1.8); 6.7513 (1.6); 3.7739 (0.8); 3.7556 (1.6); 3.7436 (3.6); 3.7329 (3.0); 3.7209 (1.2); 3.7124 (1.5); 3.3369 (64.4); 2.8902 (15.9); 2.8162 (0.4); 2.7989 (1.5); 2.7891 (2.6); 2.7734 (2.0); 2.7547 (0.3); 2.7315 (13.5); 2.5250 (0.9); 2.5115 (15.4); 2.5072 (30.2); 2.5027 (39.0); 2.4981 (28.6); 2.4937 (14.2); 2.2289 (16.0); 2.1574 (14.9); 1.2383 (0.3); −0.0002 (6.6) I-231: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.0570 (7.7); 7.9529 (1.2); 7.9202 (0.9); 7.9171 (1.5); 7.9138 (1.1); 7.9011 (1.1); 7.8976 (1.7); 7.8946 (1.2); 7.8545 (1.7); 7.8495 (2.3); 7.8451 (1.6); 7.6679 (1.2); 7.6479 (2.6); 7.6284 (1.6); 7.5797 (1.3); 7.5770 (1.4); 7.5737 (1.3); 7.5711 (1.2); 7.5594 (0.8); 7.5567 (0.8); 7.5533 (0.9); 7.5507 (0.8); 7.4513 (1.4); 7.4430 (1.4); 7.0453 (1.8); 7.0261 (2.1); 6.9084 (2.2); 6.7631 (1.2); 6.7451 (1.0); 3.8789 (16.0); 3.7624 (2.1); 3.7553 (4.1); 3.7409 (0.7); 3.7318 (0.8); 3.7230 (0.7); 3.7143 (0.5); 3.7056 (0.3); 3.3336 (34.6); 2.8913 (8.4); 2.7954 (2.2); 2.7786 (2.2); 2.7328 (7.2); 2.5256 (0.5); 2.5208 (0.7); 2.5120 (8.9); 2.5077 (17.9); 2.5031 (23.5); 2.4986 (17.4); 2.4942 (8.7); 2.2285 (10.6); 2.1677 (9.8); −0.0002 (4.3) I-232: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.3163 (0.6); 8.0320 (6.3); 8.0284 (4.2); 7.9518 (2.0); 7.4209 (1.4); 7.4100 (1.8); 7.3898 (4.1); 7.3700 (3.2); 7.3503 (1.1); 7.1979 (1.2); 7.1788 (1.1); 7.1368 (1.8); 7.1323 (1.8); 7.0992 (1.3); 7.0934 (1.0); 7.0783 (1.7); 7.0760 (1.7); 7.0728 (1.6); 7.0515 (1.9); 7.0417 (1.6); 7.0318 (1.8); 7.0268 (2.3); 7.0229 (2.4); 7.0084 (0.8); 6.9929 (0.8); 6.9872 (1.4); 6.9824 (1.2); 6.9344 (3.4); 6.8003 (0.7); 6.7873 (1.7); 6.7716 (1.3); 5.0389 (0.4); 5.0319 (0.4); 5.0237 (0.7); 5.0166 (0.7); 5.0085 (0.4); 5.0014 (0.3); 4.9623 (0.4); 4.9566 (0.4); 4.8721 (0.3); 4.8651 (0.4); 4.8570 (0.7); 4.8498 (0.7); 4.8417 (0.4); 4.8345 (0.4); 4.8024 (0.4); 4.7968 (0.4); 3.7616 (0.4); 3.7574 (0.5); 3.7337 (2.5); 3.7260 (3.6); 3.7179 (2.6); 3.7042 (1.4); 3.6973 (1.5); 3.3294 (35.0); 2.8900 (14.9); 2.7830 (2.5); 2.7766 (2.3); 2.7671 (2.4); 2.7317 (12.3); 2.7309 (12.4); 2.5402 (0.3); 2.5352 (0.4); 2.5298 (0.4); 2.5242 (1.0); 2.5192 (1.4); 2.5106 (17.7); 2.5062 (35.0); 2.5016 (45.3); 2.4970 (33.0); 2.4925 (16.2); 2.4622 (0.3); 2.4572 (0.3); 2.2314 (16.0); 2.1930 (9.9); 2.1887 (11.5); 2.1636 (0.3); 1.5820 (0.4); 1.5536 (0.3); 1.5241 (0.3); 1.5211 (0.3); 1.3932 (0.6); 1.3863 (0.6); 1.3739 (0.4); 1.3669 (0.4); 1.3358 (0.6); 1.3288 (0.6); 1.3167 (0.4); 1.3099 (0.4); 1.2912 (0.4); 1.2763 (0.5); 1.2730 (0.4); 1.2656 (0.4); 1.2577 (0.8); 1.2508 (0.6); 1.2474 (0.5); 1.2424 (0.7); 1.2392 (0.8); 1.2322 (0.8); 1.2244 (0.4); 1.2170 (0.5); 1.2138 (0.4); 1.1987 (0.3); 1.1922 (0.6); 1.1747 (0.6); 1.1650 (0.6); 1.1474 (0.5); −0.0002 (9.7) I-233: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.3161 (0.4); 8.0969 (11.6); 7.9525 (1.1); 7.8756 (4.0); 7.8540 (4.5); 7.4866 (4.2); 7.4655 (3.9); 7.4297 (2.0); 7.4220 (2.0); 7.0317 (2.7); 7.0125 (3.1); 6.9112 (3.1); 6.7618 (1.7); 6.7441 (1.5); 3.7307 (6.1); 3.7191 (1.3); 3.7096 (1.2); 3.7003 (0.8); 3.6914 (0.5); 3.3320 (81.7); 2.8911 (8.1); 2.7846 (1.6); 2.7776 (2.4); 2.7689 (1.8); 2.7609 (2.1); 2.7324 (6.8); 2.7315 (6.8); 2.6715 (0.4); 2.5250 (1.3); 2.5202 (2.0); 2.5116 (22.7); 2.5071 (45.8); 2.5026 (60.2); 2.4980 (44.2); 2.4935 (21.8); 2.3293 (0.4); 2.3250 (0.3); 2.2247 (16.0); 2.1713 (14.6); 1.2392 (0.5); 0.0080 (0.4); −0.0002 (11.4); −0.0085 (0.4) I-234: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.0690 (9.7); 7.9524 (1.9); 7.7725 (4.4); 7.7505 (4.9); 7.6366 (4.5); 7.6299 (4.8); 7.3580 (2.2); 7.3501 (2.2); 7.3430 (3.0); 7.3362 (2.6); 7.3210 (2.4); 7.3142 (2.4); 7.0391 (2.7); 7.0199 (3.2); 6.9149 (3.4); 6.7831 (1.8); 6.7639 (1.6); 3.7545 (6.3); 3.7377 (1.3); 3.7287 (1.2); 3.7191 (0.8); 3.7105 (0.5); 3.3374 (68.8); 2.8915 (12.7); 2.7897 (3.4); 2.7728 (3.3); 2.7323 (11.0); 2.5256 (0.7); 2.5120 (13.3); 2.5077 (26.4); 2.5032 (34.4); 2.4987 (25.6); 2.4944 (12.9); 2.2272 (16.0); 2.1876 (14.8); −0.0002 (5.1) I-235: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.0608 (1.2); 8.0552 (9.9); 7.9523 (2.3); 7.7732 (0.6); 7.7515 (0.6); 7.7138 (0.4); 7.6910 (3.0); 7.6876 (4.2); 7.6692 (4.6); 7.6320 (1.4); 7.6287 (1.1); 7.6124 (2.9); 7.6094 (2.1); 7.5897 (2.5); 7.5701 (3.6); 7.5577 (2.4); 7.5520 (4.2); 7.5031 (2.3); 7.4988 (1.0); 7.4849 (5.0); 7.4653 (3.1); 7.4158 (3.9); 7.4080 (2.4); 7.3975 (2.8); 7.3927 (0.8); 7.3865 (0.4); 7.3794 (0.9); 7.3477 (0.6); 7.3261 (0.6); 7.2718 (1.4); 7.2693 (1.7); 7.2664 (1.6); 7.2635 (1.5); 7.2522 (1.3); 7.2497 (1.4); 7.2468 (1.5); 7.2440 (1.3); 7.0458 (2.8); 7.0267 (3.0); 6.9375 (0.3); 6.8976 (3.2); 6.7336 (1.7); 6.7144 (1.5); 3.7970 (0.3); 3.7865 (0.8); 3.7681 (1.7); 3.7569 (2.3); 3.7515 (2.0); 3.7422 (3.1); 3.7278 (1.3); 3.7202 (2.0); 3.7012 (0.5); 3.3337 (46.3); 2.8900 (16.0); 2.7918 (3.5); 2.7750 (3.2); 2.7313 (14.1); 2.5247 (0.9); 2.5111 (15.0); 2.5069 (30.0); 2.5024 (39.7); 2.4979 (29.8); 2.4936 (15.2); 2.2434 (1.6); 2.2220 (15.3); 2.1853 (1.4); 2.1201 (14.2); −0.0002 (7.4) I-236: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.3152 (0.4); 8.0538 (11.2); 7.9521 (1.5); 7.5401 (1.8); 7.5373 (5.1); 7.5334 (6.0); 7.5304 (2.5); 7.5181 (2.4); 7.5155 (2.7); 7.5139 (2.3); 7.5110 (1.7); 7.4743 (1.9); 7.4729 (1.7); 7.4542 (3.2); 7.4514 (1.6); 7.4363 (0.9); 7.4333 (1.5); 7.3710 (2.1); 7.3628 (2.0); 7.3173 (1.9); 7.3132 (2.8); 7.3090 (1.8); 7.2970 (1.5); 7.2944 (1.5); 7.2915 (1.6); 7.2889 (1.4); 7.0399 (2.8); 7.0207 (3.2); 6.9248 (3.2); 6.7787 (1.7); 6.7611 (1.5); 3.7772 (0.4); 3.7493 (5.0); 3.7346 (1.0); 3.7261 (1.4); 3.7158 (1.0); 3.7073 (0.8); 3.6987 (0.5); 3.3375 (69.0); 2.8909 (11.2); 2.7887 (3.6); 2.7718 (3.5); 2.7326 (9.0); 2.7316 (9.3); 2.5254 (0.6); 2.5206 (1.0); 2.5119 (12.4); 2.5074 (25.0); 2.5029 (32.7); 2.4982 (23.8); 2.4937 (11.6); 2.2293 (16.0); 2.1955 (14.7); −0.0002 (3.9) I-237: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.0687 (10.4); 7.9527 (0.6); 7.6426 (1.7); 7.6217 (3.5); 7.6015 (1.9); 7.3943 (2.1); 7.3865 (2.1); 7.3517 (3.6); 7.3497 (3.5); 7.3445 (4.0); 7.3402 (2.2); 7.3242 (3.2); 7.3191 (2.1); 7.0472 (2.8); 7.0280 (3.2); 6.9155 (3.2); 6.7625 (1.7); 6.7445 (1.5); 3.7793 (0.4); 3.7510 (4.7); 3.7319 (1.2); 3.7276 (1.2); 3.7232 (1.3); 3.7131 (0.8); 3.7045 (0.5); 3.3382 (75.7); 2.8913 (4.7); 2.7901 (3.3); 2.7733 (3.1); 2.7325 (3.9); 2.5256 (0.8); 2.5208 (1.2); 2.5122 (13.8); 2.5078 (27.3); 2.5032 (35.5); 2.4986 (25.7); 2.4942 (12.4); 2.2249 (16.0); 2.1765 (14.7); −0.0002 (5.9) I-238: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.0634 (11.4); 7.9524 (0.7); 7.5080 (3.0); 7.4869 (4.4); 7.4854 (4.4); 7.4122 (2.5); 7.4033 (9.5); 7.3974 (2.6); 7.3862 (1.9); 7.3804 (5.8); 7.3716 (0.5); 7.0417 (2.8); 7.0225 (3.2); 6.9137 (3.2); 6.7530 (1.7); 6.7341 (1.5); 3.7527 (3.1); 3.7450 (5.9); 3.7290 (1.0); 3.7193 (1.2); 3.7107 (1.1); 3.7019 (0.8); 3.6932 (0.5); 3.3350 (60.0); 2.8909 (5.5); 2.7918 (3.1); 2.7748 (2.9); 2.7328 (4.3); 2.7317 (4.7); 2.5253 (0.6); 2.5206 (0.9); 2.5118 (12.8); 2.5073 (26.5); 2.5028 (35.3); 2.4982 (26.2); 2.4936 (13.1); 2.2298 (16.0); 2.1735 (14.7); 1.2394 (0.3); −0.0002 (6.9) I-239: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.1218 (10.8); 7.9530 (1.6); 7.7160 (1.1); 7.7121 (1.3); 7.7005 (1.2); 7.6961 (2.0); 7.6919 (1.4); 7.6802 (1.3); 7.6764 (1.3); 7.4717 (1.0); 7.4679 (1.1); 7.4507 (2.2); 7.4475 (1.6); 7.4333 (1.6); 7.4294 (1.6); 7.4215 (2.1); 7.4132 (2.1); 7.3203 (1.5); 7.3167 (1.5); 7.2998 (2.4); 7.2962 (2.4); 7.2793 (1.1); 7.2757 (1.0); 7.0535 (2.7); 7.0343 (3.2); 6.9228 (3.2); 6.8198 (1.7); 6.8007 (1.5); 4.2232 (0.3); 3.7688 (3.2); 3.7620 (6.3); 3.7499 (1.2); 3.7415 (1.2); 3.7321 (1.1); 3.7234 (0.8); 3.7144 (0.5); 3.3363 (64.6); 2.8916 (11.3); 2.8506 (0.4); 2.8327 (0.4); 2.8159 (1.6); 2.8043 (2.4); 2.7878 (1.9); 2.7705 (0.4); 2.7333 (9.2); 2.7323 (9.6); 2.5261 (0.6); 2.5213 (1.0); 2.5126 (13.8); 2.5081 (27.7); 2.5036 (36.2); 2.4990 (26.6); 2.4945 (13.1); 2.2399 (16.0); 2.1882 (14.6); 1.2385 (0.4); 0.9132 (0.6); −0.0002 (5.9) I-240: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.0671 (12.0); 7.9525 (0.9); 7.6758 (8.3); 7.6692 (2.9); 7.6597 (4.3); 7.6497 (0.4); 7.6394 (0.9); 7.5521 (0.4); 7.5475 (1.6); 7.5410 (2.5); 7.5333 (1.6); 7.5317 (1.4); 7.5265 (1.3); 7.5243 (1.4); 7.5185 (1.1); 7.4203 (2.1); 7.4122 (2.1); 7.0521 (2.8); 7.0329 (3.2); 6.9157 (3.3); 6.7652 (1.7); 6.7461 (1.5); 3.7559 (5.4); 3.7447 (1.2); 3.7342 (1.3); 3.7278 (1.2); 3.7176 (0.8); 3.7087 (0.5); 3.3336 (54.1); 2.8911 (6.2); 2.7941 (3.2); 2.7774 (3.0); 2.7329 (5.2); 2.7317 (5.2); 2.5253 (0.7); 2.5206 (1.1); 2.5118 (13.6); 2.5074 (27.4); 2.5028 (35.9); 2.4982 (26.3); 2.4937 (12.9); 2.2258 (16.0); 2.1762 (14.7); −0.0002 (7.2) I-241: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.3142 (0.5); 8.0412 (9.8); 7.9520 (1.8); 7.6963 (1.1); 7.6921 (2.3); 7.6868 (1.6); 7.6705 (5.4); 7.3636 (2.1); 7.3552 (2.1); 7.3205 (0.8); 7.3151 (0.6); 7.3045 (2.8); 7.3000 (6.9); 7.2949 (2.6); 7.2825 (2.9); 7.2621 (0.8); 7.0384 (2.8); 7.0192 (3.2); 6.9300 (3.2); 6.7815 (1.7); 6.7634 (1.5); 3.7777 (0.4); 3.7490 (4.2); 3.7263 (1.0); 3.7202 (1.4); 3.7115 (1.1); 3.7032 (0.8); 3.6943 (0.5); 3.3662 (0.4); 3.3397 (87.8); 3.3178 (0.5); 2.8911 (13.0); 2.7859 (3.7); 2.7689 (3.6); 2.7321 (11.0); 2.5253 (0.8); 2.5206 (1.1); 2.5119 (14.0); 2.5075 (27.9); 2.5030 (36.5); 2.4984 (26.7); 2.4940 (13.1); 2.2301 (16.0); 2.2044 (14.7); 0.9128 (0.3); −0.0002 (3.3) I-242: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.7889 (2.6); 8.7848 (2.7); 8.0704 (9.8); 8.0439 (0.4); 7.9539 (2.1); 7.8755 (1.3); 7.8717 (1.8); 7.8537 (6.1); 7.8509 (6.0); 7.6893 (1.5); 7.6681 (3.0); 7.6481 (1.5); 7.4533 (2.1); 7.4453 (2.1); 7.3335 (1.9); 7.3293 (1.8); 7.3148 (1.4); 7.3111 (2.0); 7.3073 (1.4); 7.3023 (0.4); 7.0926 (3.5); 7.0862 (3.4); 7.0469 (2.8); 7.0278 (3.2); 6.8975 (3.3); 6.7597 (1.8); 6.7397 (1.6); 3.7935 (0.6); 3.7752 (1.9); 3.7659 (3.9); 3.7577 (3.2); 3.7448 (0.9); 3.7359 (1.6); 3.7255 (1.1); 3.7169 (0.8); 3.7081 (0.5); 3.3361 (56.7); 2.8923 (15.0); 2.7942 (3.6); 2.7774 (3.5); 2.7335 (12.8); 2.5268 (1.0); 2.5219 (1.3); 2.5133 (16.1); 2.5089 (31.8); 2.5044 (41.2); 2.4998 (29.9); 2.4954 (14.6); 2.2257 (16.0); 2.2056 (0.7); 2.1225 (14.8); 1.2384 (0.4); 0.9137 (0.4); −0.0002 (6.7) I-243: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1687 (5.4); 7.9487 (1.2); 7.9226 (1.5); 7.9205 (1.4); 7.7716 (0.4); 7.7289 (1.7); 7.7253 (1.6); 7.7183 (2.3); 7.7118 (1.5); 7.7032 (2.5); 7.6768 (1.3); 7.3811 (1.2); 7.3786 (1.1); 7.3733 (1.1); 7.3538 (1.0); 7.3461 (1.0); 7.2985 (7.2); 7.0645 (0.4); 6.9873 (1.8); 6.9619 (2.2); 6.9320 (2.2); 6.7494 (1.2); 6.7243 (1.0); 6.0714 (1.5); 4.3139 (0.8); 4.3043 (1.0); 4.2791 (1.1); 4.2696 (1.0); 3.9113 (0.6); 3.9024 (0.6); 3.8952 (0.6); 3.8885 (0.6); 3.8796 (0.6); 3.8657 (1.9); 3.8455 (0.6); 3.8310 (1.3); 3.8105 (0.8); 3.1418 (15.4); 3.1202 (0.4); 3.0554 (0.7); 3.0401 (0.7); 3.0103 (1.0); 2.9941 (1.0); 2.7618 (1.0); 2.7305 (0.9); 2.7165 (0.8); 2.6846 (0.8); 2.3505 (0.9); 2.3360 (1.0); 2.3035 (11.6); 2.1975 (10.9); 2.0444 (16.0); 1.6222 (3.0); 1.2899 (1.7); 0.0366 (5.4); 0.0348 (7.5) I-244: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1453 (8.4); 7.2987 (4.6); 7.0274 (2.5); 7.0019 (3.0); 6.9271 (2.9); 6.7491 (1.6); 6.7238 (1.3); 6.1505 (1.9); 4.2900 (1.0); 4.2809 (1.4); 4.2555 (1.5); 4.2463 (1.3); 3.9247 (0.5); 3.9126 (0.6); 3.9066 (0.8); 3.8959 (0.8); 3.8898 (0.8); 3.8841 (0.7); 3.8751 (0.8); 3.8654 (2.8); 3.8458 (0.8); 3.8308 (1.9); 3.8109 (1.2); 3.0433 (0.9); 3.0277 (0.9); 2.9984 (1.4); 2.9816 (1.3); 2.7965 (1.3); 2.7657 (1.3); 2.7512 (1.2); 2.7200 (1.0); 2.3476 (12.9); 2.3460 (12.7); 2.3078 (16.0); 2.2337 (14.9); 2.2087 (0.5); 2.0448 (0.4); 1.6518 (1.2); 0.0365 (5.6) I-245: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.9043 (5.1); 7.3247 (3.0); 7.3206 (2.8); 7.2614 (12.0); 7.1435 (2.4); 7.1272 (2.7); 7.1043 (0.7); 7.0885 (1.8); 7.0726 (1.2); 7.0325 (1.0); 7.0295 (1.0); 7.0161 (1.4); 7.0022 (0.7); 6.9994 (0.6); 6.8967 (1.7); 6.8925 (1.6); 6.8804 (1.5); 6.8762 (1.4); 6.8254 (0.9); 6.8230 (0.9); 6.8099 (1.5); 6.7965 (0.8); 6.1556 (1.4); 4.1483 (1.1); 4.1420 (1.2); 4.1265 (1.4); 4.1201 (1.4); 4.0004 (0.5); 3.9942 (0.8); 3.9852 (0.8); 3.9767 (0.8); 3.9670 (0.4); 3.9247 (1.5); 3.9154 (1.1); 3.9029 (1.2); 3.8935 (1.0); 3.4877 (14.0); 3.4371 (0.8); 3.1551 (1.0); 3.1450 (1.0); 3.1281 (1.3); 3.1180 (1.2); 2.9585 (1.3); 2.9402 (1.3); 2.9315 (1.0); 2.9132 (0.9); 2.6681 (0.6); 2.6423 (16.0); 2.0867 (0.6); 2.0800 (0.7); 2.0699 (1.2); 2.0596 (0.7); 2.0530 (0.6); 2.0055 (5.0); 1.5712 (1.1); 1.2427 (0.3); 1.0396 (0.5); 1.0304 (2.1); 1.0269 (2.2); 1.0240 (1.8); 1.0134 (2.2); 1.0099 (2.1); 1.0009 (0.6); 0.7834 (1.5); 0.7808 (1.3); 0.7771 (1.4); 0.7734 (2.2); 0.7701 (2.2); 0.7680 (2.2); 0.7579 (1.3); −0.0002 (14.6) I-246: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.9040 (4.8); 7.4760 (2.6); 7.4726 (2.7); 7.2609 (11.5); 7.1091 (0.8); 7.0929 (1.8); 7.0835 (1.7); 7.0772 (1.4); 7.0673 (3.4); 7.0424 (1.9); 7.0391 (2.0); 7.0269 (1.7); 7.0231 (1.2); 7.0138 (1.5); 6.9998 (0.6); 6.8255 (0.9); 6.8122 (1.4); 6.7985 (0.7); 6.1529 (1.4); 4.1455 (1.0); 4.1392 (1.2); 4.1237 (1.3); 4.1174 (1.4); 3.9967 (0.4); 3.9900 (0.7); 3.9812 (0.8); 3.9727 (0.8); 3.9253 (1.4); 3.9159 (1.1); 3.9034 (1.2); 3.8941 (0.9); 3.4856 (0.5); 3.4375 (0.4); 3.1423 (1.0); 3.1322 (1.0); 3.1153 (1.2); 3.1052 (1.2); 2.9460 (1.2); 2.9277 (1.2); 2.9192 (1.0); 2.9008 (0.9); 2.6680 (1.0); 2.6418 (14.6); 2.0943 (0.6); 2.0875 (0.6); 2.0775 (1.1); 2.0674 (0.7); 2.0606 (0.6); 2.0052 (16.0); 1.5580 (10.7); 1.0338 (1.8); 1.0304 (2.0); 1.0169 (2.0); 1.0135 (2.0); 1.0044 (0.6); 0.7884 (1.3); 0.7781 (2.1); 0.7736 (2.2); 0.7635 (1.4); −0.0002 (14.0) I-247: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.9036 (3.8); 7.4760 (2.2); 7.4725 (2.1); 7.2612 (7.6); 7.1099 (0.6); 7.0933 (1.4); 7.0838 (1.4); 7.0777 (1.0); 7.0675 (2.6); 7.0426 (1.7); 7.0390 (1.6); 7.0268 (1.4); 7.0228 (0.9); 7.0138 (1.1); 6.9997 (0.5); 6.8255 (0.7); 6.8124 (1.1); 6.7989 (0.6); 6.1559 (1.1); 4.1452 (0.8); 4.1389 (0.9); 4.1234 (1.0); 4.1171 (1.0); 3.9965 (0.4); 3.9900 (0.6); 3.9811 (0.6); 3.9726 (0.6); 3.9253 (1.1); 3.9160 (0.8); 3.9034 (0.9); 3.8942 (0.7); 3.1423 (0.8); 3.1322 (0.8); 3.1153 (1.0); 3.1052 (0.9); 2.9463 (0.9); 2.9279 (0.9); 2.9194 (0.8); 2.9010 (0.7); 2.6660 (1.1); 2.6415 (11.4); 2.0945 (0.5); 2.0878 (0.5); 2.0776 (0.9); 2.0675 (0.6); 2.0608 (0.5); 2.0050 (16.0); 1.5636 (5.5); 1.0339 (1.5); 1.0305 (1.6); 1.0170 (1.6); 1.0135 (1.6); 1.0044 (0.4); 0.7885 (1.1); 0.7786 (1.8); 0.7755 (1.8); 0.7736 (1.8); 0.7638 (1.0); −0.0002 (9.4) I-248: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9692 (5.4); 7.2990 (7.5); 7.1670 (2.0); 7.1402 (3.8); 7.1202 (0.7); 7.1099 (0.3); 7.0970 (1.6); 7.0937 (1.6); 7.0704 (1.1); 7.0674 (1.2); 7.0193 (0.9); 7.0135 (1.1); 6.9953 (1.1); 6.9904 (1.3); 6.9687 (0.6); 6.9632 (0.6); 6.9381 (1.3); 6.9323 (1.2); 6.9123 (1.0); 6.9068 (1.0); 6.8563 (0.8); 6.8507 (0.7); 6.8298 (1.3); 6.8080 (0.7); 6.8029 (0.6); 6.2922 (1.5); 5.3361 (4.3); 5.0228 (1.5); 5.0169 (1.5); 5.0030 (1.8); 4.9959 (2.6); 4.9890 (1.7); 4.9751 (1.8); 4.9692 (1.7); 4.6478 (1.5); 4.6308 (2.0); 4.6257 (2.3); 4.6088 (2.4); 4.5889 (1.5); 4.2779 (0.6); 4.2699 (1.1); 4.2447 (1.2); 4.2368 (0.7); 4.1932 (0.7); 4.1694 (2.1); 4.1456 (2.1); 4.1219 (0.8); 4.0971 (0.3); 4.0737 (0.7); 4.0695 (0.7); 4.0463 (1.1); 4.0232 (0.6); 4.0190 (0.6); 3.9960 (0.4); 3.9345 (0.5); 3.9233 (0.6); 3.9174 (0.6); 3.8945 (1.8); 3.8607 (1.6); 3.8413 (0.9); 3.0768 (0.6); 3.0613 (0.6); 3.0318 (1.1); 3.0158 (1.1); 2.8565 (0.8); 2.8415 (1.0); 2.8253 (0.8); 2.8111 (0.7); 2.7801 (0.6); 2.6683 (16.0); 2.3741 (11.8); 2.1360 (0.5); 2.1250 (0.6); 2.1080 (1.0); 2.0820 (9.9); 2.0627 (0.4); 1.3195 (2.6); 1.2957 (5.2); 1.2719 (2.4); 1.0979 (0.7); 1.0836 (1.6); 1.0769 (1.9); 1.0701 (1.1); 1.0630 (1.2); 1.0550 (1.7); 1.0485 (1.8); 1.0348 (1.0); 0.8358 (0.9); 0.8218 (2.0); 0.8179 (2.0); 0.8091 (1.3); 0.8047 (2.0); 0.8007 (1.9); 0.7839 (0.8); 0.1063 (2.4); 0.0359 (9.0); 0.0251 (0.4) I-249: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9706 (5.1); 7.2989 (7.3); 7.2037 (0.4); 7.1955 (0.5); 7.1887 (0.5); 7.1642 (0.7); 7.1512 (0.5); 7.1352 (1.1); 7.1078 (4.3); 7.0817 (3.9); 7.0597 (0.5); 7.0332 (1.3); 7.0289 (1.3); 7.0052 (4.0); 6.9834 (0.7); 6.9788 (0.7); 6.8551 (0.9); 6.8315 (1.4); 6.8065 (0.9); 6.7876 (1.7); 6.7615 (1.3); 6.2972 (1.8); 5.3356 (2.2); 4.2640 (1.3); 4.2388 (1.4); 4.1687 (0.6); 4.1453 (0.5); 4.1225 (0.4); 4.1137 (0.4); 4.1005 (0.4); 4.0806 (1.0); 4.0681 (0.9); 4.0540 (2.0); 4.0401 (2.0); 4.0264 (2.2); 4.0095 (1.4); 3.9979 (1.2); 3.9761 (0.4); 3.9494 (1.1); 3.9427 (1.0); 3.9228 (1.8); 3.9163 (1.8); 3.8912 (2.2); 3.8793 (2.4); 3.8730 (2.4); 3.8469 (1.9); 3.8275 (1.0); 3.7598 (0.4); 3.7472 (0.4); 3.7217 (0.4); 3.6010 (0.8); 3.5747 (1.3); 3.5660 (0.8); 3.5476 (0.8); 3.5392 (1.3); 3.5121 (0.8); 3.2613 (0.6); 3.2527 (0.6); 3.2348 (0.8); 3.2265 (0.9); 3.2086 (0.6); 3.2004 (0.6); 3.0544 (0.9); 3.0397 (0.8); 3.0095 (1.4); 2.9941 (1.3); 2.8392 (1.2); 2.8232 (1.0); 2.8053 (0.5); 2.7919 (1.3); 2.7782 (0.8); 2.7522 (1.8); 2.7344 (0.6); 2.7105 (0.3); 2.6970 (0.6); 2.6852 (1.0); 2.6668 (16.0); 2.6393 (0.4); 2.3911 (0.5); 2.3615 (2.3); 2.3452 (13.5); 2.3176 (1.3); 2.3056 (0.8); 2.2889 (0.8); 2.2791 (0.9); 2.2639 (0.9); 2.2537 (0.7); 2.2379 (0.7); 2.2287 (0.4); 2.2136 (0.4); 2.1674 (0.4); 2.1498 (0.6); 2.1378 (0.8); 2.1222 (1.2); 2.1057 (1.0); 2.0938 (1.0); 2.0821 (2.4); 2.0415 (0.4); 1.9072 (0.8); 1.8797 (1.1); 1.8663 (0.7); 1.8524 (0.8); 1.8388 (0.9); 1.8114 (0.7); 1.3196 (0.5); 1.2956 (1.2); 1.2719 (0.4); 1.0961 (0.7); 1.0817 (1.7); 1.0753 (2.0); 1.0613 (1.5); 1.0535 (2.1); 1.0468 (2.5); 1.0335 (1.5); 1.0170 (0.8); 1.0102 (0.8); 0.9964 (0.6); 0.9717 (0.4); 0.8335 (0.8); 0.8184 (2.3); 0.8015 (2.4); 0.7973 (2.4); 0.7548 (0.4); 0.1751 (0.8); 0.1611 (0.8); 0.1359 (0.4); 0.1070 (2.6); 0.0470 (0.3); 0.0363 (9.0) I-250: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.9038 (4.0); 7.3244 (2.3); 7.3203 (2.2); 7.2611 (8.6); 7.1433 (1.8); 7.1270 (2.0); 7.1027 (0.6); 7.0869 (1.4); 7.0711 (1.0); 7.0321 (0.7); 7.0291 (0.8); 7.0153 (1.1); 7.0017 (0.5); 6.9990 (0.5); 6.8966 (1.3); 6.8926 (1.2); 6.8804 (1.1); 6.8763 (1.0); 6.8225 (0.8); 6.8094 (1.2); 6.7960 (0.6); 6.1544 (1.2); 4.1478 (0.9); 4.1415 (0.9); 4.1260 (1.1); 4.1196 (1.1); 4.0000 (0.4); 3.9936 (0.6); 3.9846 (0.7); 3.9761 (0.6); 3.9698 (0.4); 3.9665 (0.4); 3.9240 (1.2); 3.9146 (0.9); 3.9021 (1.0); 3.8928 (0.7); 3.1546 (0.8); 3.1446 (0.8); 3.1277 (1.0); 3.1176 (1.0); 2.9581 (1.0); 2.9397 (1.0); 2.9311 (0.8); 2.9128 (0.7); 2.6671 (1.0); 2.6415 (12.2); 2.0863 (0.5); 2.0795 (0.6); 2.0695 (0.9); 2.0593 (0.6); 2.0526 (0.5); 2.0050 (16.0); 1.5617 (4.4); 1.0392 (0.4); 1.0301 (1.6); 1.0267 (1.6); 1.0237 (1.4); 1.0132 (1.8); 1.0098 (1.6); 1.0073 (1.3); 1.0007 (0.4); 0.7831 (1.2); 0.7807 (1.1); 0.7730 (1.9); 0.7702 (1.9); 0.7677 (1.9); 0.7577 (1.1); −0.0002 (10.4) I-251: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.5985 (0.4); 7.5723 (1.4); 7.5483 (2.6); 7.5221 (0.4); 7.4533 (2.1); 7.4300 (0.9); 7.4231 (1.3); 7.4076 (0.6); 7.3992 (0.8); 7.2988 (13.4); 7.0495 (1.5); 7.0253 (3.4); 6.9558 (1.4); 6.9312 (0.9); 5.3375 (0.5); 4.8697 (1.2); 4.6754 (1.3); 4.2116 (0.9); 4.1856 (1.1); 3.9738 (0.6); 3.9440 (1.7); 3.9129 (1.4); 3.9081 (1.8); 3.8964 (0.7); 3.8852 (3.7); 3.8629 (2.0); 3.6653 (0.4); 3.6570 (0.4); 3.6492 (0.6); 3.5716 (0.6); 3.5635 (0.4); 3.5563 (0.4); 3.5422 (0.3); 3.4180 (1.8); 3.4080 (0.6); 3.3912 (3.6); 3.3719 (14.5); 3.3555 (0.4); 3.3211 (0.3); 3.2013 (1.7); 3.1789 (3.4); 3.1563 (1.6); 3.0378 (0.5); 3.0220 (0.5); 2.9919 (1.0); 2.9762 (0.9); 2.9139 (0.9); 2.8842 (0.8); 2.8678 (0.5); 2.8379 (0.4); 2.6049 (1.1); 2.6004 (1.2); 2.5933 (2.4); 2.5723 (0.4); 2.5326 (0.7); 2.4878 (11.2); 2.3210 (16.0); 2.2881 (0.6); 2.2705 (0.4); 2.2557 (0.4); 2.0445 (0.6); 1.6878 (0.5); 1.6675 (0.5); 1.2918 (0.5); 0.2209 (0.5); 0.2068 (0.5); 0.1930 (0.8); 0.1848 (1.0); 0.1775 (1.0); 0.1634 (1.1); 0.1072 (0.4); 0.0481 (0.4); 0.0373 (11.1); 0.0264 (0.6) I-252: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9788 (6.3); 7.4090 (0.8); 7.4004 (0.9); 7.3850 (1.4); 7.3765 (1.2); 7.3612 (1.1); 7.3549 (1.2); 7.2989 (12.1); 7.2101 (0.8); 7.1826 (2.1); 7.1789 (2.0); 7.1557 (3.0); 7.1381 (1.6); 7.1318 (1.9); 7.1108 (0.8); 7.1045 (0.7); 7.0361 (0.4); 7.0187 (2.5); 6.9932 (3.0); 6.9478 (0.4); 6.9077 (3.0); 6.7283 (1.6); 6.7046 (1.3); 6.0997 (1.8); 4.3227 (1.0); 4.3128 (1.2); 4.2877 (1.4); 4.2779 (1.3); 4.1942 (1.1); 4.1704 (3.4); 4.1466 (3.4); 4.1228 (1.3); 4.1014 (0.4); 3.9218 (0.9); 3.9058 (0.9); 3.8998 (0.8); 3.8900 (0.8); 3.8814 (0.8); 3.8694 (2.4); 3.8486 (1.1); 3.8346 (1.8); 3.8136 (1.2); 3.0519 (0.9); 3.0366 (1.0); 3.0183 (1.6); 3.0071 (1.5); 2.9928 (5.4); 2.9677 (4.6); 2.9423 (1.7); 2.7823 (1.4); 2.7507 (1.4); 2.7374 (1.2); 2.7051 (1.0); 2.3338 (0.8); 2.3088 (15.1); 2.2420 (0.8); 2.2168 (0.5); 2.1848 (14.2); 2.1182 (0.3); 2.0840 (16.0); 1.6703 (0.5); 1.6486 (0.5); 1.6213 (0.3); 1.3943 (4.9); 1.3691 (10.1); 1.3437 (4.8); 1.3207 (4.0); 1.2969 (8.0); 1.2731 (4.0); 0.9721 (0.5); 0.0472 (0.3); 0.0364 (14.5); 0.0257 (0.8) I-253: ¹H-NMR(300.2 MHz, CDCl3): δ = 9.0325 (0.6); 9.0159 (0.6); 8.1695 (7.8); 8.1306 (0.6); 8.1141 (0.6); 7.6278 (5.3); 7.6105 (4.3); 7.5822 (0.3); 7.3626 (2.8); 7.3148 (1.3); 7.2988 (14.4); 7.2911 (1.6); 7.2768 (0.7); 7.0043 (2.6); 6.9787 (3.0); 6.9208 (3.2); 6.7060 (1.8); 6.6806 (1.5); 6.1911 (2.0); 5.1198 (2.9); 5.0996 (4.4); 5.0916 (3.4); 5.0713 (4.7); 5.0238 (2.4); 5.0154 (2.4); 5.0017 (3.4); 4.9936 (3.3); 4.9809 (1.8); 4.9726 (1.7); 4.6289 (0.5); 4.6063 (1.1); 4.6010 (1.0); 4.5835 (0.7); 4.5783 (1.8); 4.5556 (0.8); 4.5501 (0.8); 4.5275 (0.3); 4.3517 (1.1); 4.3423 (1.4); 4.3168 (1.4); 4.3069 (1.5); 3.9470 (0.6); 3.9311 (0.8); 3.9140 (0.9); 3.9034 (0.7); 3.8977 (0.7); 3.8734 (2.5); 3.8522 (1.1); 3.8384 (1.9); 3.8171 (1.2); 3.0667 (1.0); 3.0523 (1.0); 3.0214 (1.4); 3.0064 (1.3); 2.7607 (1.6); 2.7279 (1.5); 2.7153 (1.3); 2.6821 (1.2); 2.3047 (16.0); 2.1844 (15.0); 1.6327 (1.8); 1.2913 (0.6); 1.2565 (1.9); 1.2361 (1.9); 0.0471 (0.5); 0.0363 (12.9); 0.0254 (0.5) I-254: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.0397 (4.6); 7.5998 (2.7); 7.5824 (2.4); 7.3536 (1.4); 7.2989 (12.3); 7.2798 (0.9); 7.2733 (0.8); 7.2670 (0.5); 7.2588 (0.4); 7.0023 (1.5); 6.9768 (1.7); 6.9206 (1.7); 6.7170 (0.9); 6.6913 (0.8); 6.1224 (1.1); 4.3288 (0.6); 4.3196 (0.8); 4.2943 (0.8); 4.2843 (0.8); 3.9211 (0.4); 3.9029 (0.5); 3.8867 (0.4); 3.8803 (0.4); 3.8715 (0.4); 3.8631 (1.5); 3.8417 (0.8); 3.8346 (1.8); 3.8283 (1.4); 3.8132 (4.2); 3.7919 (2.1); 3.4322 (0.3); 3.3682 (16.0); 3.2259 (2.0); 3.2046 (3.9); 3.1832 (1.7); 3.0504 (0.6); 3.0357 (0.6); 3.0051 (0.8); 2.9897 (0.8); 2.7572 (0.8); 2.7247 (0.8); 2.7119 (0.7); 2.6789 (0.6); 2.2995 (9.4); 2.1898 (8.7); 1.6101 (4.1); 1.2916 (0.4); 0.0476 (0.4); 0.0368 (12.2); 0.0260 (0.5) I-255: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.0465 (8.3); 7.6130 (4.5); 7.5961 (3.9); 7.3514 (2.6); 7.2987 (23.2); 7.2882 (1.6); 7.2853 (1.5); 7.2671 (0.7); 7.0004 (2.4); 6.9749 (2.8); 6.9184 (2.9); 6.7065 (1.6); 6.6823 (1.3); 6.1588 (2.0); 4.3427 (1.2); 4.3328 (1.3); 4.3073 (1.5); 4.2976 (1.4); 4.2616 (1.6); 4.2363 (2.3); 4.2332 (2.3); 4.2080 (2.1); 4.1365 (0.6); 4.1176 (0.7); 4.1084 (1.4); 4.0905 (1.5); 4.0811 (1.0); 4.0626 (0.9); 4.0185 (1.2); 3.9941 (2.5); 3.9694 (1.7); 3.9661 (1.8); 3.9537 (1.5); 3.9487 (1.6); 3.9412 (1.5); 3.9301 (2.2); 3.9252 (2.9); 3.9202 (1.8); 3.9016 (1.8); 3.8967 (1.8); 3.8677 (2.5); 3.8467 (1.1); 3.8328 (2.0); 3.8115 (1.3); 3.8031 (0.6); 3.7787 (1.4); 3.7507 (1.5); 3.7264 (1.2); 3.7021 (0.4); 3.0588 (1.0); 3.0446 (1.0); 3.0138 (1.4); 2.9987 (1.3); 2.7572 (1.2); 2.7239 (1.2); 2.7122 (1.0); 2.6785 (0.9); 2.4983 (0.4); 2.4805 (0.4); 2.4715 (0.5); 2.4563 (0.9); 2.4390 (0.7); 2.4295 (1.0); 2.4127 (0.8); 2.4034 (0.6); 2.3862 (0.6); 2.3454 (0.7); 2.3190 (1.8); 2.3013 (16.0); 2.2776 (1.1); 2.2533 (0.9); 2.2293 (0.4); 2.1831 (14.7); 1.6145 (4.4); 1.2913 (0.9); 1.2574 (0.3); 0.0471 (1.0); 0.0363 (20.6); 0.0253 (0.9) I-256: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.0537 (6.4); 7.6303 (4.7); 7.6132 (4.1); 7.5857 (0.6); 7.4773 (0.5); 7.3582 (2.8); 7.2987 (13.1); 7.2846 (1.9); 7.2712 (1.1); 7.0018 (2.6); 6.9763 (3.0); 6.9481 (0.4); 6.9166 (3.2); 6.7033 (1.8); 6.6787 (1.5); 6.1610 (2.2); 4.3441 (1.1); 4.3349 (1.3); 4.3094 (1.4); 4.2996 (1.5); 3.9182 (0.9); 3.9071 (1.0); 3.8904 (0.8); 3.8653 (2.3); 3.8440 (1.2); 3.8302 (1.8); 3.8089 (1.2); 3.3168 (2.2); 3.2922 (5.1); 3.2678 (3.2); 3.0619 (1.1); 3.0478 (1.2); 3.0170 (1.5); 3.0019 (1.6); 2.9892 (3.6); 2.9648 (5.4); 2.9401 (2.4); 2.7542 (1.4); 2.7214 (1.4); 2.7090 (1.3); 2.6755 (1.1); 2.3430 (1.1); 2.3296 (1.0); 2.3026 (16.0); 2.2459 (0.7); 2.1794 (14.2); 2.0906 (0.4); 1.9021 (0.4); 1.8946 (0.4); 1.8823 (0.4); 1.6454 (1.4); 1.5037 (0.4); 1.4813 (0.5); 1.4733 (0.5); 1.4629 (0.6); 1.4258 (0.5); 1.2907 (0.6); 1.2583 (0.4); 0.2277 (1.2); 0.2010 (1.2); 0.1948 (1.1); 0.1698 (0.7); 0.1402 (0.4); 0.0362 (9.4) I-257: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.8888 (6.4); 7.5502 (5.4); 7.5403 (3.9); 7.5235 (0.5); 7.3135 (3.1); 7.2604 (8.7); 7.2494 (1.4); 7.2444 (1.5); 7.2381 (1.6); 7.2347 (1.5); 7.2269 (0.9); 6.9573 (2.7); 6.9421 (2.9); 6.8797 (3.4); 6.6718 (2.0); 6.6567 (1.7); 6.1097 (2.3); 4.2785 (1.5); 4.2718 (1.5); 4.2569 (1.6); 4.2503 (1.5); 3.8842 (0.8); 3.8765 (1.1); 3.8651 (1.1); 3.8573 (0.9); 3.8129 (2.0); 3.8001 (1.4); 3.7913 (1.7); 3.7786 (1.3); 3.0032 (5.8); 2.9968 (2.3); 2.9879 (7.2); 2.9691 (1.6); 2.9599 (1.5); 2.7526 (0.7); 2.7369 (1.4); 2.7213 (1.9); 2.7059 (2.8); 2.6863 (1.7); 2.6789 (1.5); 2.6588 (1.2); 2.3126 (0.4); 2.3040 (0.5); 2.2584 (16.0); 2.2326 (0.4); 2.1511 (15.4); 2.0891 (0.8); 2.0743 (1.7); 2.0667 (1.9); 2.0575 (2.0); 2.0528 (1.9); 2.0470 (1.5); 2.0430 (1.6); 2.0322 (0.8); 2.0277 (0.8); 1.9137 (0.3); 1.8921 (0.7); 1.8731 (1.6); 1.8659 (1.5); 1.8589 (2.5); 1.8566 (2.5); 1.8494 (1.5); 1.8407 (2.5); 1.8293 (1.2); 1.7903 (1.0); 1.7874 (1.0); 1.7710 (1.9); 1.7516 (2.2); 1.7340 (1.5); 1.7177 (0.5); 1.5735 (4.6); 1.3333 (0.4); 1.2840 (0.7); 1.2554 (3.3); 1.2178 (0.5); 0.8934 (0.4); 0.8804 (0.5); 0.8662 (0.5); 0.8582 (0.8); 0.8455 (1.0); −0.0002 (9.0) I-258: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1576 (9.5); 7.6702 (1.0); 7.6645 (1.1); 7.6519 (1.1); 7.6451 (1.9); 7.6386 (1.4); 7.6262 (1.2); 7.6203 (1.3); 7.5680 (0.4); 7.5158 (0.9); 7.5100 (0.9); 7.4918 (1.1); 7.4880 (2.0); 7.4826 (1.5); 7.4646 (1.7); 7.4586 (1.4); 7.4133 (1.9); 7.4097 (1.8); 7.3858 (2.1); 7.3836 (2.2); 7.3600 (1.0); 7.3561 (1.0); 7.2988 (9.8); 7.0064 (2.5); 6.9810 (3.0); 6.9174 (2.9); 6.7366 (1.6); 6.7105 (1.3); 5.9193 (1.9); 4.3410 (1.2); 4.3320 (1.4); 4.3057 (1.5); 4.2966 (1.5); 3.9502 (0.6); 3.9432 (0.7); 3.9374 (0.8); 3.9332 (0.8); 3.9271 (0.8); 3.9216 (0.8); 3.9167 (0.9); 3.9006 (0.7); 3.8932 (0.7); 3.8793 (2.6); 3.8588 (1.1); 3.8442 (2.0); 3.8236 (1.3); 3.0662 (1.1); 3.0506 (1.0); 3.0209 (1.4); 3.0048 (1.3); 2.7760 (1.5); 2.7439 (1.4); 2.7307 (1.2); 2.6981 (1.1); 2.3646 (0.6); 2.3412 (0.7); 2.3088 (16.0); 2.2090 (2.6); 2.1925 (15.0); 2.0454 (4.6); 1.6023 (7.3); 0.0477 (0.5); 0.0369 (12.3); 0.0260 (0.6) I-259: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.9086 (5.4); 7.3117 (2.9); 7.2648 (1.2); 7.0812 (0.7); 7.0671 (3.9); 7.0517 (3.6); 7.0158 (0.9); 7.0127 (1.1); 6.9989 (1.5); 6.9856 (0.6); 6.9826 (0.6); 6.8065 (0.8); 6.8038 (0.8); 6.7909 (1.5); 6.7777 (0.8); 6.7751 (0.7); 6.7318 (1.5); 6.7165 (1.4); 6.1799 (1.6); 4.1825 (1.1); 4.1758 (1.2); 4.1606 (1.3); 4.1540 (1.4); 4.0174 (0.5); 4.0110 (0.7); 4.0052 (0.7); 4.0023 (0.8); 3.9997 (0.8); 3.9940 (0.8); 3.9880 (0.6); 3.9839 (0.4); 3.8817 (1.4); 3.8711 (1.2); 3.8598 (1.2); 3.8492 (1.1); 3.1430 (0.9); 3.1328 (1.0); 3.1161 (1.2); 3.1059 (1.1); 2.9028 (1.2); 2.8843 (1.2); 2.8759 (1.0); 2.8574 (0.9); 2.6296 (16.0); 2.1631 (12.3); 2.0869 (0.6); 2.0802 (0.7); 2.0700 (1.1); 2.0598 (0.7); 2.0531 (0.6); 1.9962 (0.6); 1.6990 (1.2); 1.0292 (1.0); 1.0252 (1.6); 1.0224 (2.0); 1.0172 (1.6); 1.0147 (1.5); 1.0087 (1.7); 1.0054 (2.0); 1.0013 (1.2); 0.7772 (1.2); 0.7738 (1.2); 0.7683 (1.9); 0.7650 (2.0); 0.7624 (2.2); 0.7547 (1.2); 0.7519 (1.3); −0.0002 (1.7) I-260: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1222 (16.0); 7.4002 (6.2); 7.3933 (6.4); 7.2990 (9.6); 7.2957 (4.2); 7.2896 (5.5); 7.2862 (4.7); 7.2684 (9.9); 7.2625 (6.5); 7.2054 (4.3); 7.1782 (7.4); 7.1121 (4.8); 7.1051 (4.6); 7.0849 (2.7); 7.0779 (2.6); 5.9521 (2.5); 5.9445 (2.5); 4.1739 (2.1); 4.1639 (2.6); 4.1379 (3.0); 4.1280 (3.6); 4.0768 (0.4); 4.0616 (0.8); 4.0482 (1.4); 4.0435 (1.1); 4.0373 (1.4); 4.0329 (1.7); 4.0221 (1.7); 4.0127 (1.0); 4.0040 (1.0); 3.9940 (0.6); 3.9732 (3.8); 3.9582 (2.3); 3.9374 (2.5); 3.9223 (1.9); 3.1891 (1.7); 3.1709 (1.7); 3.1439 (3.2); 3.1256 (3.0); 3.0485 (3.2); 3.0194 (3.1); 3.0034 (1.8); 2.9741 (1.8); 2.2035 (2.1); 1.6101 (3.9); 0.9966 (0.3); 0.1070 (0.5); 0.0469 (0.4); 0.0360 (10.9); 0.0252 (0.4) I-261: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1225 (16.0); 7.5511 (6.7); 7.5447 (6.8); 7.3106 (4.6); 7.3051 (6.4); 7.2988 (12.4); 7.2617 (4.3); 7.2558 (12.0); 7.2501 (8.0); 7.2347 (5.0); 7.2282 (4.6); 7.1396 (7.4); 7.1124 (4.8); 5.9485 (2.9); 5.9416 (2.9); 4.1726 (2.2); 4.1627 (2.7); 4.1367 (3.2); 4.1269 (3.7); 4.0750 (0.5); 4.0598 (1.0); 4.0462 (1.6); 4.0418 (1.4); 4.0350 (1.6); 4.0310 (1.9); 4.0203 (1.8); 4.0117 (1.2); 4.0023 (1.2); 3.9921 (0.8); 3.9753 (4.0); 3.9604 (2.4); 3.9395 (2.7); 3.9245 (2.0); 3.1765 (1.8); 3.1586 (1.8); 3.1315 (3.4); 3.1133 (3.1); 3.0375 (3.4); 3.0085 (3.2); 2.9925 (1.9); 2.9632 (1.8); 2.2045 (6.1); 2.0417 (3.8); 1.6129 (1.9); 0.1065 (0.6); 0.0465 (0.8); 0.0359 (13.5); 0.0250 (0.6) I-262: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1526 (0.5); 8.1431 (8.7); 7.5304 (0.5); 7.5257 (0.7); 7.5238 (0.7); 7.5199 (0.6); 7.5011 (1.5); 7.4830 (0.7); 7.4783 (1.0); 7.4731 (0.7); 7.2988 (3.9); 7.2668 (2.2); 7.2406 (1.8); 7.2274 (1.0); 7.2248 (1.1); 7.2209 (1.2); 7.2011 (1.4); 7.1992 (1.4); 7.1745 (0.6); 7.0107 (2.5); 6.9852 (2.9); 6.9105 (3.0); 6.7154 (1.6); 6.6906 (1.4); 6.1589 (2.0); 4.3121 (1.0); 4.3037 (1.4); 4.2777 (1.5); 4.2692 (1.2); 3.9222 (0.5); 3.9052 (0.8); 3.8951 (0.7); 3.8895 (0.8); 3.8824 (0.7); 3.8664 (2.9); 3.8464 (0.7); 3.8321 (1.9); 3.8116 (1.1); 3.0533 (0.9); 3.0383 (0.9); 3.0086 (1.4); 2.9924 (1.3); 2.7778 (1.2); 2.7466 (1.2); 2.7326 (1.1); 2.7010 (1.0); 2.3086 (16.0); 2.1616 (15.0); 2.0412 (1.9); 1.6467 (1.4); 1.5431 (0.6); 1.5171 (2.1); 1.4968 (0.8); 1.4802 (0.6); 1.4538 (2.1); 1.4335 (0.8); 1.2289 (0.6); 1.2221 (0.5); 1.2052 (2.2); 1.1989 (2.4); 1.1754 (2.6); 1.1688 (1.9); 1.1523 (0.4); 1.1457 (0.4); 0.0383 (3.8) I-263: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.4738 (0.3); 7.4483 (0.5); 7.4269 (0.4); 7.3453 (0.6); 7.3217 (0.5); 7.3191 (0.4); 7.2987 (17.9); 7.2791 (0.7); 7.2528 (0.7); 7.0508 (0.8); 7.0246 (2.1); 6.9477 (0.8); 6.9225 (0.4); 4.7748 (0.7); 4.2165 (0.6); 4.1909 (0.7); 3.9375 (0.9); 3.9238 (0.4); 3.9071 (0.7); 2.9959 (0.5); 2.9788 (0.5); 2.9038 (0.5); 2.8746 (0.4); 2.5591 (9.3); 2.3245 (6.2); 2.3065 (5.8); 2.0460 (16.0); 1.5902 (7.6); 1.4943 (0.8); 1.4312 (0.8); 1.4090 (0.3); 1.1862 (0.8); 1.1792 (0.9); 1.1565 (0.9); 0.0483 (0.8); 0.0375 (21.6); 0.0266 (0.7) I-264: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1623 (1.6); 7.6310 (0.9); 7.6277 (1.0); 7.6229 (0.5); 7.6098 (0.6); 7.5867 (1.1); 7.5616 (3.1); 7.5563 (1.7); 7.5374 (0.4); 7.5093 (1.7); 7.4814 (0.8); 7.4740 (1.2); 7.4668 (0.6); 7.4593 (0.5); 7.4567 (0.5); 7.4509 (0.7); 7.4436 (0.4); 7.3508 (0.4); 7.2988 (6.7); 7.0805 (1.2); 7.0549 (2.3); 7.0410 (1.9); 7.0011 (1.3); 6.9755 (0.7); 6.9631 (0.6); 6.9180 (0.5); 5.6422 (1.1); 4.1494 (0.9); 4.1235 (1.0); 3.9395 (0.4); 3.9314 (0.6); 3.9081 (1.7); 3.8938 (0.7); 3.8854 (0.6); 3.8765 (1.3); 3.8592 (0.9); 3.8249 (0.4); 3.8040 (0.3); 3.7236 (0.9); 3.7188 (0.9); 3.7034 (2.0); 3.6852 (1.0); 3.6790 (1.0); 3.1836 (0.8); 3.1624 (1.4); 3.1510 (1.6); 3.1433 (0.9); 3.1318 (0.8); 3.1035 (0.4); 3.0884 (16.0); 2.9193 (1.0); 2.8990 (1.8); 2.8721 (0.9); 2.3372 (10.2); 2.3197 (9.5); 2.2971 (3.0); 2.1801 (2.6); 1.4843 (0.6); 1.4720 (0.7); 1.2926 (0.5); 0.1087 (0.4); 0.0380 (6.9) I-265: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.5506 (0.5); 7.5351 (1.7); 7.5196 (4.4); 7.5047 (0.6); 7.4170 (2.6); 7.3727 (1.6); 7.3584 (1.2); 7.2591 (3.2); 6.9995 (3.0); 6.9852 (1.8); 6.9698 (2.8); 6.9247 (1.9); 6.9095 (1.2); 4.6809 (1.9); 4.1229 (1.0); 4.1171 (1.2); 4.1013 (1.3); 4.0954 (1.3); 3.9300 (0.8); 3.9201 (0.9); 3.9134 (0.9); 3.9081 (0.7); 3.9027 (0.6); 3.8927 (1.7); 3.8830 (0.8); 3.8709 (1.2); 3.8612 (0.9); 3.5416 (0.8); 3.5232 (1.2); 3.5052 (0.8); 2.9721 (0.7); 2.9616 (0.8); 2.9444 (1.3); 2.9337 (1.2); 2.8718 (1.3); 2.8539 (1.2); 2.8443 (0.8); 2.8261 (0.8); 2.2822 (15.0); 2.2782 (16.0); 2.2594 (0.4); 2.1659 (0.6); 2.1486 (1.1); 2.1391 (1.2); 2.1314 (1.2); 2.0996 (0.4); 1.9969 (0.6); 1.9659 (2.4); 1.9581 (2.2); 1.9410 (1.6); 1.7424 (1.4); 1.7353 (1.5); 1.5712 (2.3); 1.2562 (0.4); −0.0002 (3.7) I-266: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.5347 (1.2); 7.5107 (3.3); 7.4871 (0.3); 7.4209 (1.6); 7.3758 (0.7); 7.3682 (1.2); 7.3610 (0.6); 7.3544 (0.4); 7.3516 (0.5); 7.3455 (0.7); 7.3381 (0.4); 7.2989 (4.3); 7.0283 (1.8); 7.0111 (0.9); 6.9855 (2.5); 6.9612 (1.4); 6.9354 (0.5); 5.9718 (0.7); 5.9573 (0.4); 5.0851 (1.1); 5.0801 (1.2); 4.1354 (0.6); 4.1239 (0.7); 4.0987 (0.8); 4.0872 (0.8); 3.9200 (0.3); 3.9111 (0.4); 3.9004 (0.5); 3.8920 (0.6); 3.8818 (0.5); 3.8726 (0.4); 3.8061 (1.0); 3.7868 (0.7); 3.7696 (0.9); 3.7503 (0.8); 3.7288 (16.0); 3.6910 (0.8); 3.6739 (0.9); 3.6555 (0.8); 3.6371 (0.7); 3.6146 (0.4); 2.9907 (0.5); 2.9706 (0.5); 2.9445 (0.8); 2.9244 (0.8); 2.8125 (0.8); 2.7847 (0.8); 2.7665 (0.6); 2.7385 (0.5); 2.5322 (1.5); 2.5095 (3.2); 2.4868 (1.8); 2.3163 (9.2); 2.2988 (9.8); 2.1019 (0.5); 2.0793 (1.6); 2.0567 (2.2); 2.0341 (1.4); 2.0112 (0.3); 1.6466 (0.6); 0.0374 (4.8) I-267: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.5571 (0.5); 7.5311 (2.0); 7.5074 (5.6); 7.4842 (0.6); 7.4414 (2.8); 7.3855 (1.1); 7.3780 (1.9); 7.3709 (1.1); 7.3643 (0.7); 7.3552 (1.2); 7.2989 (9.1); 7.0345 (3.2); 7.0089 (1.2); 6.9833 (4.5); 6.9690 (2.8); 6.9409 (0.7); 6.0630 (0.8); 6.0451 (1.5); 6.0263 (0.8); 5.2446 (2.0); 4.1009 (0.9); 4.0907 (1.1); 4.0652 (1.2); 4.0549 (1.3); 3.8906 (0.7); 3.8806 (0.8); 3.8718 (0.9); 3.8643 (0.9); 3.8438 (0.6); 3.8306 (1.9); 3.8129 (0.8); 3.7947 (1.3); 3.7770 (0.9); 3.5758 (0.5); 3.5568 (0.5); 3.5314 (1.8); 3.5123 (2.0); 3.5051 (1.8); 3.4852 (1.4); 3.4604 (0.4); 3.4411 (0.4); 2.9973 (0.8); 2.9773 (0.8); 2.9519 (1.4); 2.9309 (1.3); 2.8350 (1.3); 2.8090 (1.3); 2.7892 (0.8); 2.7627 (0.8); 2.5402 (1.2); 2.3208 (15.1); 2.2944 (16.0); 1.6456 (2.7); 1.3312 (15.6); 1.3194 (15.9); 1.2921 (1.0); 1.2648 (0.3); 1.2587 (0.4); 0.1079 (0.7); 0.0375 (10.6); 0.0267 (0.5) I-268: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.0565 (2.3); 8.0535 (2.4); 8.0477 (2.5); 8.0448 (2.2); 7.6358 (2.5); 7.6320 (2.5); 7.6269 (2.2); 7.6188 (5.2); 7.6154 (5.7); 7.6009 (0.4); 7.4929 (2.7); 7.4722 (0.4); 7.4650 (0.4); 7.4584 (1.2); 7.4454 (1.6); 7.4385 (1.5); 7.4283 (1.1); 7.4198 (0.7); 7.2988 (13.8); 7.0904 (0.4); 7.0679 (0.4); 7.0350 (2.3); 7.0095 (6.4); 6.9330 (2.0); 6.9074 (1.1); 6.8841 (3.2); 6.8753 (3.2); 6.8595 (0.4); 6.8504 (0.3); 5.0046 (1.8); 4.9954 (1.8); 3.9002 (1.1); 3.8895 (1.4); 3.8643 (1.3); 3.8537 (2.1); 3.8236 (0.8); 3.8132 (0.8); 3.8050 (0.8); 3.7957 (0.8); 3.7861 (0.6); 3.7757 (0.5); 3.7289 (0.5); 3.7022 (1.8); 3.6863 (1.4); 3.6664 (1.3); 3.6506 (1.0); 2.9169 (0.5); 2.8970 (0.6); 2.8705 (1.8); 2.8462 (2.4); 2.8166 (1.7); 2.7992 (0.5); 2.7706 (0.5); 2.3586 (1.7); 2.3415 (1.6); 2.3119 (15.1); 2.2947 (16.0); 2.0813 (0.7); 1.6469 (0.6); 1.2929 (0.8); 0.1088 (1.4); 0.0491 (0.5); 0.0458 (0.4); 0.0383 (16.6); 0.0290 (0.6); 0.0274 (0.7) I-269: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.5276 (0.5); 7.5007 (2.3); 7.4805 (6.0); 7.4613 (0.6); 7.4224 (3.0); 7.3812 (0.4); 7.3651 (1.3); 7.3553 (1.7); 7.3476 (1.4); 7.3342 (1.2); 7.3268 (0.7); 7.2984 (18.0); 7.0145 (3.7); 6.9918 (1.4); 6.9662 (4.6); 6.9495 (3.0); 6.9236 (0.8); 6.0218 (0.8); 6.0053 (1.6); 5.9887 (0.8); 5.3805 (1.7); 4.1931 (0.8); 4.1693 (2.5); 4.1455 (2.5); 4.1218 (1.0); 4.1006 (0.4); 4.0844 (1.0); 4.0730 (1.1); 4.0479 (1.2); 4.0368 (1.2); 3.8627 (1.0); 3.7884 (1.6); 3.7699 (1.1); 3.7516 (1.3); 3.7329 (1.1); 3.7014 (0.7); 3.6796 (1.2); 3.6622 (1.4); 3.6419 (1.4); 3.6232 (1.1); 3.6010 (0.7); 3.5803 (0.4); 3.0141 (0.4); 3.0010 (0.4); 2.9523 (1.3); 2.9322 (1.4); 2.9069 (2.0); 2.8858 (2.0); 2.8132 (2.5); 2.7866 (2.6); 2.7672 (2.1); 2.7406 (1.9); 2.5335 (2.3); 2.5121 (3.9); 2.4900 (2.5); 2.3738 (0.4); 2.3080 (16.0); 2.2717 (16.0); 2.1158 (1.3); 2.0829 (11.9); 2.0523 (2.0); 2.0307 (2.6); 2.0089 (1.6); 1.9868 (0.5); 1.4680 (1.6); 1.3195 (3.1); 1.2957 (6.3); 1.2719 (3.1); 1.2571 (1.0); 0.1057 (9.4); 0.0934 (0.4); 0.0462 (1.0); 0.0354 (22.9); 0.0261 (0.7); 0.0246 (0.8) I-270: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1526 (10.5); 7.6416 (0.6); 7.6284 (5.6); 7.6253 (6.4); 7.6162 (2.4); 7.6052 (2.9); 7.5788 (0.7); 7.3624 (3.2); 7.3441 (1.1); 7.3126 (19.1); 7.2990 (7.2); 7.2822 (1.0); 7.2529 (1.3); 7.2457 (1.8); 7.2369 (0.9); 7.2312 (1.6); 7.2239 (1.8); 7.2149 (0.9); 6.7125 (2.2); 6.5247 (4.3); 6.3369 (2.1); 6.1198 (2.2); 5.3355 (5.7); 4.2806 (1.4); 4.2715 (1.8); 4.2458 (2.0); 4.2365 (1.8); 4.1909 (0.9); 4.1671 (2.8); 4.1433 (2.8); 4.1200 (1.4); 4.0987 (1.2); 4.0764 (0.6); 3.9684 (0.7); 3.9594 (0.8); 3.9517 (0.9); 3.9430 (0.9); 3.9363 (1.0); 3.9276 (1.0); 3.9189 (1.0); 3.9083 (3.4); 3.8900 (1.1); 3.8735 (2.4); 3.8547 (1.4); 3.1250 (1.0); 3.1100 (1.0); 3.0806 (1.5); 3.0646 (1.4); 2.8740 (1.6); 2.8431 (1.6); 2.8295 (1.4); 2.7980 (1.2); 2.0928 (0.4); 2.0796 (16.0); 2.0392 (1.8); 1.6690 (0.5); 1.6467 (0.7); 1.6376 (0.7); 1.6205 (1.2); 1.5988 (0.5); 1.4288 (0.4); 1.4041 (0.4); 1.3184 (3.5); 1.2945 (7.7); 1.2708 (3.3); 0.9957 (1.0); 0.9790 (0.4); 0.9712 (2.0); 0.9469 (0.8); 0.1074 (2.0); 0.0361 (8.0); 0.0252 (0.3) I-271: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1283 (9.7); 7.4820 (1.8); 7.4545 (3.9); 7.4270 (2.3); 7.2991 (1.4); 7.1318 (1.5); 7.1294 (1.3); 7.1262 (1.5); 7.1246 (1.5); 7.1042 (1.2); 7.1016 (1.1); 7.0988 (1.3); 6.9948 (2.5); 6.9693 (3.0); 6.9439 (1.6); 6.9413 (2.0); 6.9338 (4.4); 6.9168 (1.3); 6.9142 (1.4); 6.9093 (1.7); 6.9067 (1.7); 6.8745 (2.0); 6.8671 (3.2); 6.8600 (1.5); 6.8252 (2.2); 6.7383 (1.6); 6.7130 (1.3); 6.5809 (4.6); 6.3365 (2.3); 6.1467 (1.9); 5.3310 (0.5); 4.3019 (1.1); 4.2919 (1.3); 4.2668 (1.5); 4.2576 (1.4); 3.9149 (0.5); 3.9085 (0.6); 3.9031 (0.7); 3.8987 (0.7); 3.8927 (0.7); 3.8878 (0.7); 3.8822 (0.8); 3.8758 (0.6); 3.8731 (0.6); 3.8662 (0.7); 3.8582 (0.7); 3.8466 (2.5); 3.8260 (1.0); 3.8118 (1.9); 3.7910 (1.2); 3.0447 (1.0); 3.0295 (1.0); 2.9994 (1.4); 2.9836 (1.3); 2.7524 (1.4); 2.7206 (1.4); 2.7072 (1.2); 2.6748 (1.1); 2.2965 (16.0); 2.2161 (14.9); 1.6829 (4.2); 0.0412 (1.7) I-272: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1079 (9.0); 7.2991 (0.8); 7.1374 (3.4); 7.1091 (4.0); 7.0066 (2.5); 6.9811 (3.1); 6.9411 (3.0); 6.8138 (2.9); 6.8069 (4.8); 6.7971 (3.6); 6.7891 (1.6); 6.7686 (3.3); 6.7608 (3.4); 6.7377 (1.4); 6.1056 (2.2); 4.3091 (1.2); 4.2990 (1.3); 4.2738 (1.5); 4.2637 (1.4); 3.9259 (0.5); 3.9192 (0.6); 3.9097 (0.8); 3.9035 (0.7); 3.8930 (0.8); 3.8872 (0.6); 3.8767 (0.6); 3.8698 (0.5); 3.8610 (0.4); 3.8438 (2.3); 3.8230 (1.2); 3.8084 (1.8); 3.7876 (1.2); 3.0525 (1.0); 3.0368 (1.0); 3.0071 (1.4); 2.9910 (1.3); 2.7532 (1.5); 2.7207 (1.4); 2.7078 (1.2); 2.6749 (1.1); 2.3035 (16.0); 2.2287 (15.0); 2.1965 (0.9); 2.0299 (2.6); 0.0402 (0.8) I-273: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9511 (5.2); 7.6284 (2.2); 7.4035 (1.4); 7.3774 (2.0); 7.2987 (8.3); 7.2179 (1.4); 7.1914 (1.0); 7.1348 (0.6); 7.1079 (1.6); 7.0812 (1.4); 7.0528 (1.0); 7.0467 (1.1); 7.0290 (1.1); 7.0239 (1.2); 7.0024 (0.6); 6.9967 (0.5); 6.8555 (0.7); 6.8496 (0.7); 6.8290 (1.2); 6.8074 (0.7); 6.8019 (0.6); 6.2083 (1.2); 6.2012 (1.2); 5.3366 (9.0); 4.1933 (0.8); 4.1838 (1.1); 4.1580 (1.4); 4.1489 (1.4); 4.0865 (0.4); 4.0753 (0.6); 4.0599 (0.7); 4.0461 (0.6); 4.0266 (1.9); 4.0131 (0.7); 3.9916 (1.0); 3.9777 (0.7); 3.3038 (0.6); 3.2888 (0.6); 3.2599 (1.1); 3.2440 (1.0); 3.1217 (1.0); 3.0920 (1.0); 3.0776 (0.8); 3.0474 (0.7); 2.6832 (16.0); 2.6373 (0.6); 2.1128 (0.5); 2.1014 (0.6); 2.0835 (1.2); 2.0671 (0.6); 2.0562 (0.5); 1.6032 (9.0); 1.2964 (0.5); 1.0803 (0.4); 1.0660 (1.6); 1.0591 (1.9); 1.0485 (1.0); 1.0444 (0.9); 1.0374 (1.7); 1.0309 (1.8); 1.0196 (0.7); 0.8115 (0.9); 0.7957 (2.0); 0.7889 (1.8); 0.7795 (2.1); 0.7725 (1.3): 0.7620 (0.8); 0.1074 (2.9); 0.0480 (0.4); 0.0372 (11.6); 0.0264 (0.5) I-274: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.1159 (5.7); 7.5661 (1.2); 7.5528 (4.0); 7.5377 (2.4); 7.5286 (1.6); 7.5125 (2.1); 7.4969 (0.9); 7.2596 (19.4); 7.2071 (6.5); 7.1994 (4.9); 7.0789 (0.8); 7.0710 (1.4); 7.0627 (2.6); 7.0556 (2.1); 7.0468 (1.9); 6.8197 (4.3); 6.1876 (1.8); 5.2984 (4.6); 4.3560 (1.1); 4.3490 (1.2); 4.3342 (1.2); 4.3273 (1.3); 4.0189 (0.5); 4.0110 (0.7); 4.0055 (0.7); 3.9990 (0.8); 3.9914 (0.6); 3.8370 (1.4); 3.8240 (1.2); 3.8152 (1.4); 3.8022 (1.2); 3.4563 (16.0); 3.1722 (0.9); 3.1628 (1.0); 3.1436 (1.2); 3.1343 (1.2); 2.8727 (1.2); 2.8527 (1.2); 2.8442 (1.1); 2.8242 (1.0); 2.0050 (0.3); 1.7880 (0.7); 1.6424 (0.3); 1.6022 (0.4); 1.5920 (0.4); 1.5778 (0.4); 1.5651 (0.4); 1.5424 (0.5); 1.5250 (0.3); 1.4218 (0.3); 1.3208 (0.3); 1.3078 (0.4); 1.2838 (0.5); 1.2546 (3.5); 1.2317 (0.6); 1.2159 (0.5); 0.8802 (0.5); 0.8579 (1.1); 0.8451 (1.5); −0.0002 (24.2) I-275: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1152 (6.1); 7.2988 (2.8); 7.1320 (1.6); 7.1064 (2.0); 7.0016 (1.7); 6.9761 (2.0); 6.9334 (2.0); 6.8585 (1.2); 6.8514 (1.5); 6.8322 (1.0); 6.8252 (1.3); 6.7823 (2.1); 6.7757 (1.9); 6.7340 (1.1); 6.7087 (0.9); 6.2953 (1.3); 4.2905 (0.7); 4.2822 (0.9); 4.2569 (1.0); 4.2475 (0.8); 3.8998 (0.3); 3.8887 (0.4); 3.8828 (0.5); 3.8727 (0.5); 3.8675 (0.5); 3.8607 (0.5); 3.8438 (1.9); 3.8235 (0.5); 3.8095 (1.3); 3.7887 (0.8); 3.2373 (16.0); 3.0421 (0.6); 3.0266 (0.6); 2.9973 (1.0); 2.9808 (0.9); 2.7581 (0.8); 2.7272 (0.8); 2.7127 (0.8); 2.6816 (0.7); 2.3019 (10.8); 2.2288 (10.0); 1.6484 (0.5); 0.0401 (2.9) I-276: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1422 (10.2); 7.2988 (2.9); 7.2744 (1.3); 7.2714 (1.3); 7.2681 (1.2); 7.2530 (3.1); 7.2292 (2.1); 7.2245 (2.2); 7.2011 (0.7); 7.1966 (1.0); 7.1093 (1.4); 7.1030 (1.4); 7.0875 (1.4); 7.0825 (1.2); 7.0783 (1.6); 7.0635 (1.0); 7.0544 (0.9); 7.0087 (2.5); 6.9832 (3.0); 6.9093 (2.8); 6.8612 (1.9); 6.7297 (1.6); 6.7045 (1.3); 6.6187 (3.9); 6.3762 (2.0); 6.0757 (1.9); 4.3131 (1.1); 4.3040 (1.4); 4.2782 (1.4); 4.2692 (1.4); 3.9279 (0.5); 3.9207 (0.6); 3.9158 (0.7); 3.9107 (0.8); 3.9041 (0.7); 3.8999 (0.7); 3.8948 (0.8); 3.8883 (0.6); 3.8789 (0.8); 3.8651 (2.8); 3.8448 (0.9); 3.8304 (2.0); 3.8099 (1.2); 3.0530 (1.0); 3.0375 (1.0); 3.0080 (1.4); 2.9916 (1.3); 2.7770 (1.4); 2.7457 (1.3); 2.7320 (1.2); 2.7001 (1.1); 2.3039 (16.0); 2.1724 (15.0); 1.6681 (0.8); 0.0389 (2.3) I-277: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.0748 (0.4); 8.0680 (0.5); 7.8830 (4.3); 7.8780 (4.2); 7.5795 (4.6); 7.5625 (4.2); 7.5346 (0.5); 7.5111 (0.4); 7.3519 (0.4); 7.3180 (2.6); 7.2987 (37.3); 7.2865 (0.7); 7.2703 (1.0); 7.2629 (1.0); 7.2541 (1.4); 7.2473 (1.1); 7.2401 (0.9); 7.2321 (0.8); 7.0338 (0.4); 6.9962 (2.3); 6.9708 (2.7); 6.9153 (2.9); 6.7144 (1.6); 6.6886 (1.3); 6.1638 (0.3); 6.1296 (1.9); 4.3200 (1.0); 4.3097 (1.2); 4.2854 (1.3); 4.2755 (1.2); 3.9493 (0.3); 3.9080 (0.9); 3.8952 (0.9); 3.8800 (0.8); 3.8580 (2.0); 3.8365 (1.0); 3.8234 (1.4); 3.8024 (1.0); 3.3985 (0.6); 3.3901 (0.4); 3.1339 (0.5); 3.0424 (1.0); 3.0281 (0.9); 2.9973 (1.3); 2.9819 (1.2); 2.7557 (1.3); 2.7243 (1.3); 2.7113 (1.1); 2.6775 (1.0); 2.3576 (0.4); 2.3285 (1.3); 2.2957 (16.0); 2.1859 (14.4); 1.9616 (0.5); 1.9437 (1.0); 1.9295 (1.0); 1.9155 (1.1); 1.9007 (0.6); 1.6002 (9.7); 1.5465 (1.6); 1.5320 (1.5); 1.5171 (1.4); 1.4969 (1.3); 1.4810 (0.8); 1.4591 (0.5); 1.4210 (0.3); 1.3242 (1.0); 1.3169 (1.1); 1.2938 (4.0); 1.2794 (1.5); 1.2720 (1.3); 1.2629 (1.0); 1.2557 (0.9); 1.1671 (0.3); 0.9797 (0.4); 0.9663 (1.1); 0.9522 (1.6); 0.9478 (1.5); 0.9365 (1.9); 0.9187 (2.0); 0.8980 (1.1); 0.8718 (0.4); 0.4991 (0.6); 0.4847 (1.4); 0.4696 (1.6); 0.4553 (1.8); 0.4423 (1.4); 0.4278 (0.8); 0.4088 (0.4); 0.3980 (0.4); 0.2215 (0.5); 0.1939 (1.9); 0.1833 (2.2); 0.1074 (0.9); 0.0487 (1.2); 0.0379 (45.2); 0.0287 (2.3); 0.0271 (2.4); −0.0022 (0.4); −0.0301 (0.3) I-278: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.5541 (0.5); 7.5384 (1.4); 7.5255 (3.4); 7.5230 (3.5); 7.5110 (0.5); 7.3864 (2.0); 7.3488 (1.3); 7.3446 (1.3); 7.3404 (0.9); 7.3348 (1.0); 7.3308 (1.0); 7.2600 (11.3); 7.0032 (2.4); 6.9998 (2.3); 6.9883 (2.9); 6.9222 (0.9); 6.9059 (0.6); 6.8957 (0.9); 6.8801 (0.6); 4.7032 (1.0); 4.6853 (0.9); 4.2035 (0.5); 4.1972 (0.6); 4.1818 (0.6); 4.1752 (0.7); 4.1602 (0.7); 4.1447 (0.7); 3.9342 (0.4); 3.9281 (0.5); 3.9226 (0.6); 3.9051 (1.5); 3.8978 (0.9); 3.8889 (1.2); 3.8798 (1.2); 3.8685 (0.6); 3.8578 (0.7); 3.8466 (0.5); 3.8041 (0.7); 3.7816 (0.7); 3.7710 (0.6); 3.7483 (0.6); 3.0127 (0.4); 3.0027 (0.5); 2.9917 (0.6); 2.9847 (0.7); 2.9809 (0.8); 2.9752 (0.6); 2.9641 (0.6); 2.9528 (0.6); 2.8642 (0.6); 2.8475 (0.6); 2.8367 (0.4); 2.8184 (0.8); 2.8002 (0.6); 2.7900 (0.5); 2.7723 (0.4); 2.3743 (0.4); 2.3691 (0.4); 2.3251 (0.9); 2.2820 (16.0); 2.2760 (8.2); 1.8252 (0.4); 1.8132 (0.7); 1.8102 (0.7); 1.8079 (0.7); 1.7974 (1.1); 1.7867 (0.7); 1.7846 (0.7); 1.7813 (0.8); 1.7693 (0.5); 1.5708 (2.0); 1.4769 (0.4); 1.4656 (0.6); 1.4579 (0.7); 1.4476 (0.9); 1.4391 (0.9); 1.4288 (0.7); 1.4212 (0.6); 1.4098 (0.3); 1.2840 (0.4); 1.2568 (1.7); 1.1690 (0.4); 1.1604 (0.7); 1.1522 (0.9); 1.1437 (1.0); 1.1351 (0.9); 1.1269 (0.6); 1.1181 (0.4); 1.0818 (0.5); 1.0705 (0.7); 1.0640 (0.5); 1.0588 (0.6); 1.0526 (0.6); 1.0410 (0.5); 1.0282 (0.4); 1.0169 (0.7); 1.0104 (0.5); 1.0052 (0.6); 0.9992 (0.6); 0.9874 (0.5); 0.9486 (0.6); 0.9378 (1.0); 0.9269 (1.0); 0.9201 (1.0); 0.9092 (0.9); 0.8983 (0.5); 0.8942 (0.4); 0.8802 (0.5); 0.8665 (0.4); 0.5735 (0.4); 0.5640 (0.6); 0.5553 (0.8); 0.5459 (1.0); 0.5376 (0.8); 0.5293 (0.6); 0.5199 (0.4); 0.4486 (0.4); 0.4460 (0.4); 0.4374 (0.6); 0.4348 (0.6); 0.4292 (0.8); 0.4209 (0.9); 0.4104 (0.7); 0.4026 (0.5); 0.2718 (0.4); 0.2656 (0.5); 0.2609 (0.6); 0.2577 (0.7); 0.2530 (0.8); 0.2469 (0.8); 0.2425 (0.8); 0.2385 (0.7); 0.2341 (0.7); 0.2280 (0.4); 0.2233 (0.4); 0.2037 (0.5); 0.1947 (1.0); 0.1846 (1.0); 0.1758 (0.8); 0.1658 (0.5); 0.0060 (0.8); −0.0002 (11.6); −0.0066 (0.6) I-279: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.4114 (0.5); 7.6165 (0.4); 7.5901 (1.5); 7.5688 (4.0); 7.5485 (0.5); 7.4643 (2.0); 7.4352 (0.9); 7.4264 (1.3); 7.4187 (0.8); 7.4053 (0.9); 7.2993 (16.0); 7.0382 (2.5); 7.0080 (2.8); 6.9720 (1.7); 6.9469 (0.8); 6.1375 (0.6); 6.1197 (0.5); 6.1025 (0.7); 6.0806 (0.8); 6.0628 (0.6); 6.0456 (0.8); 6.0271 (0.4); 5.5680 (1.3); 5.5636 (1.3); 5.5109 (1.1); 5.5064 (1.1); 5.4135 (1.4); 5.4100 (1.4); 5.3787 (1.2); 5.3751 (1.2); 5.3378 (1.2); 5.0691 (0.5); 5.0505 (0.5); 5.0287 (1.2); 5.0104 (1.1); 4.9858 (1.2); 4.9674 (1.1); 4.9454 (0.4); 4.9269 (0.4); 4.8564 (1.4); 4.2052 (0.9); 4.1948 (1.0); 4.1693 (1.2); 4.1592 (1.1); 3.9841 (0.3); 3.9753 (0.4); 3.9650 (0.7); 3.9553 (0.6); 3.9462 (0.8); 3.9364 (0.7); 3.9278 (0.6); 3.9081 (1.8); 3.8902 (0.7); 3.8723 (1.2); 3.8543 (0.8); 3.7191 (0.4); 3.6962 (0.5); 3.6747 (0.4); 3.1490 (0.3); 3.1244 (0.8); 3.0995 (0.8); 3.0757 (0.4); 3.0327 (0.8); 3.0141 (0.8); 2.9869 (1.3); 2.9682 (1.2); 2.8845 (1.4); 2.8557 (1.3); 2.8384 (0.9); 2.8093 (0.9); 2.7587 (0.4); 2.7508 (0.4); 2.7401 (0.4); 2.7078 (0.4); 2.6696 (0.4); 2.6378 (0.4); 2.6153 (0.4); 2.5271 (0.4); 2.5004 (0.4); 2.4102 (0.6); 2.3845 (0.6); 2.3591 (0.9); 2.3197 (16.0); 2.2518 (0.4); 2.1343 (0.5); 1.6191 (0.4); 1.5988 (0.4); 1.5734 (0.4); 1.5040 (1.1); 1.4795 (1.9); 1.4543 (6.5); 1.4322 (5.8); 1.3662 (0.5); 1.2915 (1.9); 1.2550 (0.5); 0.9587 (0.4); 0.9411 (0.4); 0.8988 (1.2); 0.8776 (1.3); 0.1073 (0.8); 0.0569 (0.3); 0.0480 (0.8); 0.0374 (14.5); 0.0268 (0.7) I-280: ¹H-NMR(400.1 MHz, CDCl3): δ = 8.0072 (2.2); 7.5345 (0.6); 7.5155 (1.8); 7.4906 (3.7); 7.4715 (0.7); 7.3897 (2.4); 7.3418 (1.6); 7.3242 (1.1); 7.2621 (19.2); 7.0038 (3.6); 6.9710 (0.6); 6.9520 (2.0); 6.9351 (3.5); 6.9076 (0.5); 6.0694 (0.5); 6.0242 (0.7); 6.0124 (0.6); 5.3007 (1.0); 5.2271 (0.6); 5.2152 (0.7); 5.2044 (0.7); 5.1924 (0.6); 5.0549 (1.0); 5.0485 (0.5); 5.0429 (1.1); 5.0369 (1.0); 5.0306 (0.5); 5.0248 (0.9); 4.9629 (0.9); 4.9110 (0.7); 4.8802 (0.8); 4.3992 (0.8); 4.3904 (1.1); 4.3820 (0.9); 4.3730 (1.0); 4.3621 (0.6); 4.2208 (0.8); 4.2044 (0.8); 4.1993 (0.9); 4.1830 (0.7); 4.1487 (0.4); 4.1401 (0.4); 4.1214 (0.9); 4.1123 (1.0); 4.1013 (0.5); 4.0930 (0.9); 4.0847 (0.7); 4.0741 (0.5); 4.0654 (0.5); 4.0012 (0.7); 3.9802 (1.3); 3.9592 (1.0); 3.9353 (0.7); 3.9247 (0.7); 3.9130 (0.5); 3.9024 (0.6); 3.8679 (1.8); 3.8612 (1.4); 3.8564 (1.4); 3.8463 (1.2); 3.8353 (0.9); 3.7757 (0.7); 3.7580 (1.1); 3.7424 (1.3); 3.7274 (1.4); 3.7149 (1.8); 3.6831 (0.6); 3.6693 (0.9); 3.6551 (0.5); 3.6463 (0.5); 3.6304 (0.5); 3.6245 (0.5); 3.6089 (0.8); 3.5933 (0.6); 3.5874 (0.7); 3.5718 (0.7); 3.5496 (0.5); 2.9552 (16.0); 2.9246 (1.1); 2.9110 (1.1); 2.8800 (13.8); 2.7663 (0.5); 2.7466 (1.0); 2.7262 (0.8); 2.7129 (0.9); 2.7054 (0.6); 2.6914 (0.5); 2.6830 (0.4); 2.2858 (13.3); 2.2651 (13.0); 1.5821 (7.6); 1.4676 (4.2); 1.4632 (4.4); 1.4557 (4.5); 1.4512 (4.2); 1.3878 (3.8); 1.3760 (3.8); 0.0077 (1.3); −0.0002 (23.6) I-281: ¹H-NMR(400.1 MHz, CDCl3): δ = 8.0124 (2.1); 7.6080 (1.2); 7.5930 (2.9); 7.5494 (0.4); 7.5386 (1.1); 7.5253 (2.0); 7.5233 (2.1); 7.4413 (1.5); 7.3952 (1.3); 7.3803 (1.0); 7.3748 (0.8); 7.3643 (0.7); 7.3417 (0.5); 7.3326 (0.6); 7.3276 (0.6); 7.3189 (0.5); 7.3129 (0.4); 7.2620 (17.5); 7.0874 (0.9); 7.0682 (1.3); 7.0095 (1.3); 6.9984 (0.4); 6.9757 (0.9); 6.9499 (1.5); 6.9304 (1.5); 6.8866 (1.6); 6.7357 (0.9); 6.7172 (0.8); 5.3006 (1.1); 5.1570 (0.8); 5.1031 (0.9); 5.0952 (1.0); 4.1073 (0.8); 4.0993 (0.8); 4.0931 (0.9); 4.0763 (1.3); 4.0710 (1.5); 4.0621 (0.7); 4.0542 (0.9); 4.0396 (0.5); 3.9280 (2.1); 3.9189 (2.9); 3.8393 (0.5); 3.8291 (0.8); 3.8204 (1.0); 3.8128 (1.0); 3.8029 (0.8); 3.7951 (0.8); 3.7768 (0.9); 3.7614 (1.2); 3.7585 (1.1); 3.7393 (1.0); 3.7203 (0.4); 3.6625 (0.6); 3.6479 (0.6); 3.6351 (0.6); 3.6206 (0.5); 2.9556 (15.6); 2.9288 (0.5); 2.9111 (0.6); 2.8934 (1.1); 2.8815 (16.0); 2.8646 (1.7); 2.7892 (0.6); 2.7703 (0.6); 2.7549 (0.4); 2.7358 (0.4); 2.6467 (0.4); 2.6282 (0.6); 2.6098 (0.5); 2.5980 (0.4); 2.5795 (0.4); 2.5739 (0.6); 2.5643 (0.5); 2.5553 (1.1); 2.5418 (0.8); 2.5372 (0.9); 2.5320 (0.7); 2.5219 (0.7); 2.5099 (1.0); 2.4990 (0.4); 2.4892 (0.8); 2.4794 (0.4); 2.4669 (0.4); 2.3710 (0.4); 2.3581 (0.8); 2.3393 (1.3); 2.3199 (2.2); 2.3027 (7.2); 2.2865 (6.3); 2.2602 (0.5); 2.2267 (11.5); 1.6067 (2.1); 1.2217 (0.5); 0.0078 (1.1); −0.0002 (21.7); −0.0083 (1.1) I-282: ¹H-NMR(400.1 MHz, CDCl3): δ = 8.0094 (1.5); 7.5258 (0.5); 7.5065 (1.4); 7.4866 (2.4); 7.4813 (2.2); 7.4618 (0.5); 7.3865 (2.0); 7.3322 (1.2); 7.3133 (0.9); 7.2622 (12.1); 7.0255 (2.5); 6.9696 (0.3); 6.9510 (5.6); 5.3007 (0.7); 4.8266 (1.1); 4.7961 (1.7); 4.7736 (16.0); 4.7026 (1.2); 4.6790 (0.8); 4.1407 (0.4); 4.1303 (0.4); 4.1227 (0.4); 3.9172 (0.6); 3.9088 (0.7); 3.9021 (0.7); 3.7101 (0.4); 2.9762 (0.8); 2.9557 (11.4); 2.9416 (1.0); 2.9272 (0.9); 2.8811 (9.8); 2.7482 (0.4); 2.7250 (0.5); 2.7147 (0.4); 2.2997 (11.6); 2.2820 (11.5); 1.5851 (5.6); 0.0078 (0.8); −0.0002 (15.1) I-283: ¹H-NMR(400.1 MHz, CDCl3): δ = 8.1232 (1.2); 8.0006 (2.1); 7.5894 (0.8); 7.5732 (0.5); 7.5614 (1.0); 7.5467 (2.4); 7.5445 (2.2); 7.5236 (0.3); 7.5041 (0.9); 7.4890 (2.1); 7.4276 (1.2); 7.4009 (0.5); 7.3931 (0.7); 7.3876 (0.6); 7.3777 (0.6); 7.3111 (1.5); 7.2620 (16.2); 7.2471 (0.8); 7.2364 (0.6); 7.0550 (1.0); 7.0358 (1.4); 6.9985 (1.4); 6.9555 (1.6); 6.9346 (1.3); 6.9270 (1.2); 6.9066 (0.6); 6.8800 (0.4); 6.8520 (0.7); 6.8342 (0.5); 5.3007 (0.8); 5.1839 (0.5); 4.7495 (0.8); 4.1962 (0.5); 4.1868 (0.6); 4.1728 (0.8); 4.1602 (0.7); 4.1537 (0.8); 3.9663 (0.5); 3.9546 (1.0); 3.9443 (0.4); 3.9330 (1.0); 3.9047 (0.4); 3.8969 (0.4); 3.8907 (0.4); 3.8812 (0.4); 3.7800 (0.7); 3.7638 (0.5); 3.7527 (0.6); 3.7365 (0.4); 3.0069 (0.4); 2.9940 (0.4); 2.9717 (1.0); 2.9542 (16.0); 2.9363 (0.8); 2.9279 (0.8); 2.9142 (1.1); 2.9013 (0.4); 2.8770 (13.9); 2.7302 (0.5); 2.7067 (0.6); 2.6967 (0.6); 2.6722 (0.6); 2.2979 (6.8); 2.2860 (6.5); 2.2752 (1.0); 2.2597 (2.8); 2.2498 (10.8); 2.1422 (2.0); 2.0614 (0.4); 1.5827 (4.2); 1.5471 (6.1); 0.9551 (0.8); 0.9477 (1.1); 0.8098 (0.4); 0.7959 (1.6); 0.0078 (0.9); −0.0002 (19.5); −0.0083 (1.0) I-284: ¹H-NMR(400.1 MHz, CDCl3): δ = 8.0097 (1.1); 7.5235 (0.7); 7.5042 (2.1); 7.4848 (3.7); 7.4801 (3.2); 7.4601 (0.7); 7.3881 (2.8); 7.3414 (1.8); 7.3225 (1.3); 7.2616 (16.3); 7.0013 (3.3); 6.9804 (1.8); 6.9612 (3.6); 6.9295 (2.2); 6.9105 (1.0); 5.8225 (0.8); 5.3006 (0.5); 4.9025 (1.8); 4.1189 (0.9); 4.1106 (1.0); 4.0913 (1.1); 4.0829 (1.1); 3.9015 (0.6); 3.8949 (0.8); 3.8873 (1.0); 3.8805 (1.0); 3.8725 (0.9); 3.8655 (0.6); 3.7940 (1.4); 3.7797 (1.0); 3.7663 (1.2); 3.7521 (1.0); 3.7308 (0.5); 3.7165 (0.8); 3.6999 (1.0); 3.6865 (0.9); 3.6698 (0.4); 3.6372 (0.7); 3.6235 (0.8); 3.6077 (0.6); 3.5925 (0.4); 2.9756 (1.0); 2.9556 (8.4); 2.9409 (1.4); 2.9265 (1.3); 2.8812 (7.1); 2.7826 (1.3); 2.7608 (1.3); 2.7481 (1.0); 2.7263 (0.9); 2.3219 (0.5); 2.3057 (0.6); 2.2844 (15.4); 2.2709 (16.0); 1.6508 (0.3); 1.6328 (0.9); 1.6157 (2.1); 1.6054 (2.2); 1.5989 (2.4); 1.5882 (2.9); 1.5747 (10.3); 0.7386 (0.6); 0.7210 (1.0); 0.7134 (0.6); 0.7017 (0.7); 0.6893 (0.4); 0.5817 (1.1); 0.5678 (3.1); 0.5567 (1.6); 0.5506 (2.8); 0.5369 (0.9); 0.1837 (1.0); 0.1709 (3.6); 0.1584 (3.4); 0.1467 (0.9); 0.0078 (1.0); −0.0002 (20.2); −0.0084 (1.0) I-285: ¹H-NMR(400.1 MHz, CDCl3): δ = 8.1252 (0.6); 8.0065 (2.0); 7.5895 (0.5); 7.5619 (0.6); 7.5472 (1.3); 7.5449 (1.3); 7.5319 (0.6); 7.5128 (1.4); 7.4946 (2.8); 7.4911 (2.6); 7.4865 (2.4); 7.4803 (3.3); 7.4272 (0.7); 7.3996 (0.4); 7.3927 (0.7); 7.3796 (1.8); 7.3473 (1.7); 7.3363 (0.9); 7.3315 (1.1); 7.3264 (0.9); 7.3130 (1.1); 7.3077 (1.1); 7.3009 (1.1); 7.2958 (0.8); 7.2838 (0.9); 7.2617 (24.3); 7.0536 (0.6); 7.0344 (0.8); 6.9910 (3.2); 6.9739 (1.3); 6.9538 (2.5); 6.9332 (2.2); 6.9077 (2.0); 6.8868 (0.8); 5.9738 (0.5); 5.9624 (0.5); 5.9476 (0.6); 5.9362 (0.6); 5.9306 (0.7); 5.9193 (0.9); 5.9045 (0.8); 5.8932 (0.9); 5.8760 (0.5); 5.8646 (0.5); 5.8499 (0.5); 5.8383 (0.5); 5.8330 (0.6); 5.8214 (0.6); 5.8068 (0.5); 5.7953 (0.6); 5.6980 (0.4); 5.6798 (0.4); 5.3006 (1.0); 5.2009 (1.0); 5.1981 (1.0); 5.1691 (1.2); 5.1576 (1.0); 5.1550 (1.0); 5.1452 (1.0); 5.1430 (1.0); 5.0845 (1.0); 5.0391 (0.9); 4.9914 (1.1); 4.9655 (1.9); 4.8942 (0.4); 4.8875 (0.4); 4.8771 (0.4); 4.8602 (0.4); 4.8459 (0.5); 4.8293 (0.5); 4.8120 (0.4); 4.7684 (1.0); 4.7249 (0.4); 4.1851 (0.8); 4.1757 (1.0); 4.1568 (1.1); 4.1498 (0.9); 4.0916 (0.6); 4.0837 (0.7); 4.0646 (0.8); 4.0564 (0.8); 3.9555 (0.6); 3.9329 (0.6); 3.8993 (0.4); 3.8851 (0.6); 3.8779 (0.7); 3.8717 (0.7); 3.8639 (0.7); 3.8576 (0.6); 3.8501 (0.5); 3.8431 (0.5); 3.8257 (1.4); 3.8126 (1.0); 3.7986 (1.1); 3.7851 (0.7); 3.7697 (1.2); 3.7536 (0.7); 3.7424 (0.9); 3.7263 (0.6); 3.1205 (2.1); 3.0703 (0.4); 2.9688 (1.1); 2.9552 (16.0); 2.9346 (1.4); 2.9267 (0.9); 2.9196 (1.0); 2.9049 (0.9); 2.8910 (1.0); 2.8796 (13.5); 2.7791 (0.9); 2.7574 (0.9); 2.7441 (0.7); 2.7209 (1.1); 2.6974 (0.8); 2.6854 (0.6); 2.6628 (0.6); 2.2969 (4.0); 2.2856 (6.5); 2.2766 (12.6); 2.2665 (11.3); 2.2564 (9.3); 2.1422 (1.1); 1.7467 (0.4); 1.7320 (0.4); 1.5776 (10.8); 1.4124 (5.0); 1.4041 (5.4); 1.3959 (5.3); 1.3876 (5.1); 0.0078 (1.4); −0.0002 (29.6); −0.0083 (1.7) I-286: ¹H-NMR(400.1 MHz, CDCl3): δ = 8.0097 (2.2); 7.5435 (0.4); 7.5232 (1.7); 7.5078 (4.1); 7.3441 (2.1); 7.2953 (0.9); 7.2886 (1.4); 7.2830 (1.1); 7.2715 (1.4); 7.2620 (17.2); 6.9892 (2.4); 6.9663 (1.5); 6.9472 (2.4); 6.8900 (1.5); 6.8710 (1.0); 6.7660 (0.4); 5.3008 (0.8); 5.1414 (1.3); 5.0232 (0.7); 5.0068 (1.6); 5.0008 (1.0); 4.9888 (1.6); 4.9836 (2.2); 4.9688 (1.8); 4.9597 (1.0); 4.9468 (0.6); 4.9298 (0.4); 4.6307 (1.0); 4.6184 (1.4); 4.6139 (1.3); 4.6019 (1.4); 4.5874 (1.5); 4.5729 (0.8); 4.2104 (0.8); 4.2010 (0.9); 4.1827 (1.0); 4.1733 (1.0); 3.9340 (0.7); 3.9253 (0.7); 3.7631 (1.2); 3.7467 (1.0); 3.7353 (1.1); 3.7192 (0.9); 3.0035 (0.8); 2.9902 (0.8); 2.9686 (1.2); 2.9563 (16.0); 2.8814 (13.8); 2.7456 (0.9); 2.7225 (1.0); 2.7109 (0.8); 2.6876 (0.7); 2.3161 (0.5); 2.2800 (11.6); 2.2645 (11.8); 2.2353 (0.4); 2.1792 (0.4); 1.6049 (1.1); −0.0002 (21.2) I-287: ¹H-NMR(400.1 MHz, CDCl3): δ = 8.0052 (1.6); 7.5403 (0.6); 7.5207 (2.2); 7.5029 (5.4); 7.4859 (0.5); 7.3696 (2.8); 7.3259 (1.1); 7.3204 (1.8); 7.3152 (1.2); 7.3032 (1.4); 7.2616 (16.6); 6.9939 (3.1); 6.9618 (1.8); 6.9427 (3.6); 6.9111 (2.2); 6.8921 (1.0); 6.0560 (0.9); 5.3005 (0.4); 5.0332 (1.9); 4.1530 (1.2); 4.1439 (1.3); 4.1253 (1.4); 4.1164 (1.4); 3.9262 (0.4); 3.9100 (0.9); 3.9049 (1.0); 3.8906 (1.7); 3.8747 (2.8); 3.8586 (3.3); 3.8424 (2.2); 3.8259 (0.8); 3.8071 (0.4); 3.7768 (1.6); 3.7617 (1.3); 3.7490 (1.4); 3.7339 (1.1); 3.0698 (0.3); 2.9761 (1.1); 2.9548 (12.2); 2.9415 (1.5); 2.9272 (1.3); 2.8790 (10.6); 2.7579 (1.4); 2.7357 (1.3); 2.7233 (1.1); 2.7010 (1.0); 2.6058 (0.4); 2.5893 (0.7); 2.5797 (1.1); 2.5732 (0.6); 2.5630 (2.0); 2.5536 (1.3); 2.5465 (1.2); 2.5368 (2.0); 2.5269 (0.6); 2.5201 (1.0); 2.5107 (0.7); 2.3170 (0.6); 2.3066 (0.8); 2.2745 (15.2); 2.2647 (16.0); 1.5748 (7.7); 0.0077 (1.1); −0.0002 (20.6); −0.0082 (1.0) I-288: ¹H-NMR(400.1 MHz, CDCl3): δ = 8.0122 (2.0); 7.5373 (0.5); 7.5183 (1.6); 7.4993 (3.4); 7.4915 (3.2); 7.4867 (3.5); 7.3734 (1.8); 7.3472 (1.7); 7.3247 (1.6); 7.3058 (1.3); 7.2996 (1.3); 7.2823 (0.8); 7.2759 (0.7); 7.2618 (22.4); 6.9842 (3.1); 6.9694 (1.5); 6.9498 (2.3); 6.9397 (1.2); 6.9186 (0.6); 6.9038 (1.6); 6.8866 (1.6); 6.8679 (0.6); 6.1756 (0.4); 6.1116 (0.4); 5.3006 (0.9); 5.0572 (0.8); 4.9332 (1.0); 4.8651 (0.3); 4.1883 (0.5); 4.1800 (0.6); 4.1612 (0.8); 4.1495 (1.1); 4.1391 (0.8); 4.1202 (1.0); 4.1117 (0.8); 3.8690 (1.0); 3.8622 (1.1); 3.8546 (1.0); 3.8482 (1.0); 3.7745 (0.8); 3.7600 (1.3); 3.7472 (1.3); 3.7325 (1.4); 3.7172 (0.7); 3.1815 (0.4); 3.1732 (0.5); 3.1641 (0.7); 3.1549 (0.5); 3.1463 (0.4); 2.9730 (0.7); 2.9562 (16.0); 2.9396 (1.9); 2.9249 (2.0); 2.9211 (2.0); 2.9069 (1.5); 2.8822 (13.6); 2.7442 (1.0); 2.7240 (1.1); 2.7126 (1.0); 2.7019 (0.7); 2.6896 (0.8); 2.3255 (0.3); 2.3054 (0.7); 2.2742 (11.3); 2.2681 (12.0); 2.2568 (14.4); 1.5762 (13.5); 1.1762 (0.5); 1.1657 (0.7); 1.1522 (0.7); 1.1427 (0.6); 1.0119 (0.4); 1.0009 (0.5); 0.9912 (0.6); 0.9797 (0.8); 0.9668 (0.7); 0.9587 (0.8); 0.9483 (0.8); 0.9380 (0.6); 0.9281 (0.4); 0.6861 (0.6); 0.6765 (0.9); 0.6624 (0.8); 0.6528 (1.3); 0.6365 (1.3); 0.6197 (0.8); 0.6029 (0.8); 0.5917 (0.7); 0.5865 (0.7); 0.5783 (0.8); 0.5697 (1.5); 0.5546 (1.1); 0.5430 (0.6); 0.5331 (0.5); 0.5207 (0.5); 0.5076 (0.8); 0.4988 (1.0); 0.4878 (1.1); 0.4770 (1.0); 0.4652 (0.9); 0.4544 (0.8); 0.4455 (0.4); 0.4054 (0.4); 0.3878 (0.9); 0.3815 (0.9); 0.3767 (1.0); 0.3674 (1.0); 0.3565 (0.6); 0.2583 (0.5); 0.2488 (0.7); 0.2437 (0.7); 0.2324 (0.6); 0.2215 (0.5); 0.2099 (0.4); 0.1989 (0.4); 0.1889 (0.4); 0.1789 (0.5); 0.1655 (0.5); 0.1548 (0.8); 0.1419 (1.1); 0.1308 (1.2); 0.1179 (1.1); 0.1073 (0.7); 0.0941 (0.4); 0.0828 (0.4); 0.0704 (0.7); 0.0544 (0.9); 0.0428 (0.9); 0.0306 (0.7); 0.0175 (0.6); −0.0002 (27.9) I-289: ¹H-NMR(400.1 MHz, CDCl3): δ = 8.0078 (1.1); 7.5305 (0.5); 7.5113 (1.4); 7.4921 (2.5); 7.4682 (0.5); 7.3925 (1.8); 7.3445 (1.1); 7.3259 (0.8); 7.2620 (10.8); 7.0016 (2.1); 6.9688 (1.0); 6.9496 (2.5); 6.9289 (1.5); 6.9082 (0.6); 6.2002 (0.7); 5.3007 (0.5); 4.9305 (1.2); 4.1389 (0.7); 4.1299 (0.7); 4.1113 (0.8); 4.1021 (0.8); 3.9096 (0.4); 3.9027 (0.5); 3.8947 (0.6); 3.8877 (0.6); 3.8805 (0.5); 3.8728 (0.4); 3.8151 (0.4); 3.7981 (0.5); 3.7795 (1.4); 3.7647 (1.1); 3.7516 (1.0); 3.7364 (0.7); 3.6957 (0.6); 3.6808 (0.6); 3.6634 (0.4); 3.6477 (0.3); 2.9686 (0.8); 2.9553 (8.8); 2.9342 (0.9); 2.9198 (0.8); 2.8802 (7.2); 2.8380 (1.0); 2.8315 (1.1); 2.8227 (1.8); 2.8161 (1.6); 2.8076 (1.1); 2.7997 (0.9); 2.7696 (0.9); 2.7476 (0.8); 2.7349 (0.6); 2.7129 (0.6); 2.3189 (0.4); 2.3048 (0.5); 2.2838 (9.7); 2.2679 (10.1); 2.1226 (16.0); 2.0998 (0.4); 1.5783 (7.4); 0.0077 (0.7); −0.0002 (13.4); −0.0084 (0.7) I-290: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9513 (5.2); 7.2991 (11.6); 7.1523 (2.4); 7.1384 (0.6); 7.1127 (3.4); 7.0870 (3.3); 7.0620 (1.0); 7.0556 (1.2); 7.0381 (1.1); 7.0333 (1.3); 7.0117 (0.6); 7.0060 (0.5); 6.8578 (0.8); 6.8520 (0.7); 6.8319 (1.2); 6.8098 (0.6); 6.8048 (0.6); 6.7423 (1.3); 6.7190 (1.2); 6.2145 (1.3); 4.2405 (1.0); 4.2294 (1.1); 4.2044 (1.2); 4.1933 (1.3); 4.0527 (0.4); 4.0416 (0.6); 4.0330 (0.6); 4.0227 (0.7); 4.0138 (0.7); 4.0040 (0.5); 3.9959 (0.4); 3.9184 (1.5); 3.9005 (1.1); 3.8823 (1.2); 3.8643 (1.0); 3.1979 (0.8); 3.1808 (0.8); 3.1532 (1.2); 3.1363 (1.1); 2.9372 (1.2); 2.9068 (1.2); 2.8927 (0.9); 2.8621 (0.8); 2.6724 (16.0); 2.2087 (11.9); 2.1399 (0.5); 2.1285 (0.6); 2.1114 (1.0); 2.0943 (0.6); 2.0829 (0.6); 2.0663 (0.3); 2.0443 (5.3); 1.6057 (3.5); 1.2933 (0.8); 1.0884 (0.7); 1.0747 (1.5); 1.0684 (1.9); 1.0557 (1.2); 1.0465 (1.6); 1.0401 (1.8); 1.0272 (0.9); 0.8828 (0.3); 0.8650 (0.3); 0.8294 (0.9); 0.8223 (0.9); 0.8133 (2.0); 0.8061 (1.9); 0.7975 (2.1); 0.7905 (1.3); 0.7803 (0.7); 0.1076 (2.6); 0.0486 (0.6); 0.0379 (15.8); 0.0271 (0.7) I-291: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9364 (0.9); 7.9278 (1.7); 7.9193 (0.9); 7.6253 (0.9); 7.6030 (2.4); 7.5108 (1.2); 7.4744 (0.5); 7.4647 (0.8); 7.4575 (0.5); 7.4431 (0.5); 7.2986 (21.0); 7.0352 (0.9); 7.0108 (2.4); 6.9479 (0.9); 6.9216 (0.5); 6.5852 (1.0); 6.5763 (1.0); 6.5715 (1.0); 6.5628 (0.9); 5.3376 (0.4); 5.0231 (0.6); 5.0077 (0.6); 4.9872 (0.3); 4.9345 (0.8); 4.0731 (0.5); 4.0523 (0.6); 4.0277 (0.3); 3.9776 (0.5); 3.9532 (1.0); 3.9429 (0.7); 3.9334 (0.6); 3.9264 (0.6); 3.9088 (0.8); 3.7656 (0.8); 3.7287 (0.7); 3.6926 (0.4); 2.8701 (0.7); 2.8503 (0.6); 2.8210 (0.5); 2.7929 (0.5); 2.3683 (0.4); 2.3564 (0.4); 2.3426 (0.6); 2.3185 (6.9); 2.3013 (7.3); 2.1150 (0.5); 2.1000 (0.9); 2.0825 (1.4); 2.0601 (0.8); 2.0446 (0.4); 1.5959 (16.0); 1.2936 (0.8); 0.0489 (0.9); 0.0473 (0.7); 0.0382 (24.5); 0.0290 (0.8); 0.0273 (0.9) I-292: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.5739 (3.6); 7.4593 (2.3); 7.4167 (1.3); 7.3005 (5.7); 7.0488 (3.4); 7.0271 (2.0); 6.9816 (1.8); 6.9551 (0.9); 4.7633 (1.9); 4.2308 (1.0); 4.1957 (1.3); 3.9545 (1.0); 3.9150 (1.3); 3.8766 (0.8); 3.0376 (0.6); 2.9959 (1.0); 2.8877 (0.9); 2.8572 (0.9); 2.8168 (0.5); 2.7403 (8.4); 2.3267 (16.0); 1.5876 (6.1); 1.3000 (0.6); 0.0403 (7.9) I-293: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.1090 (0.4); 7.9834 (4.3); 7.6876 (4.4); 7.5809 (1.0); 7.5643 (3.3); 7.5573 (5.4); 7.5360 (2.2); 7.5251 (2.4); 7.5091 (4.1); 7.4906 (1.4); 7.4700 (3.9); 7.4583 (4.1); 7.4166 (0.9); 7.4019 (2.2); 7.3871 (1.4); 7.2583 (3.4); 6.9870 (3.9); 6.9726 (2.9); 6.9566 (3.7); 6.9419 (2.9); 6.9268 (1.2); 6.8918 (0.6); 6.8775 (0.7); 5.3935 (2.0); 5.0670 (0.6); 3.8947 (1.8); 3.8789 (2.1); 3.8230 (6.0); 3.8085 (16.0); 3.7850 (15.4); 3.7509 (0.9); 3.7440 (0.8); 3.7319 (1.5); 3.7215 (2.1); 3.7010 (2.5); 3.6869 (1.4); 2.8512 (1.0); 2.8376 (1.1); 2.8331 (1.1); 2.8233 (1.5); 2.8112 (1.2); 2.7978 (0.6); 2.7805 (0.6); 2.7696 (0.4); 2.7526 (1.4); 2.7382 (1.3); 2.7250 (0.8); 2.7108 (0.6); 2.3172 (1.0); 2.2847 (13.5); 2.2750 (6.1); 2.2576 (16.0); 2.1415 (1.1); 1.7036 (0.3); 1.2561 (0.5); 0.0722 (0.9); −0.0002 (4.0) I-294: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.9328 (4.5); 7.9802 (4.3); 7.6442 (0.8); 7.5916 (7.1); 7.5234 (4.4); 7.4754 (3.2); 7.2998 (8.4); 7.1556 (0.3); 7.0126 (4.9); 6.9316 (9.8); 4.8526 (3.6); 3.9255 (1.9); 3.8947 (2.5); 3.7330 (4.4); 3.7022 (1.9); 2.8647 (1.1); 2.8202 (2.2); 2.7551 (1.7); 2.7271 (1.7); 2.6848 (0.8); 2.3159 (15.8); 2.2728 (16.0); 2.0441 (1.0); 1.6119 (8.3); 0.1096 (1.1); 0.0400 (11.3) I-295: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9357 (5.2); 7.3546 (2.6); 7.3480 (2.6); 7.2987 (16.4); 7.2130 (2.2); 7.1858 (3.2); 7.1470 (0.6); 7.1206 (1.6); 7.0940 (1.4); 7.0920 (1.4); 7.0801 (1.8); 7.0734 (1.7); 7.0653 (1.1); 7.0589 (1.3); 7.0529 (1.3); 7.0456 (1.4); 7.0416 (1.3); 7.0378 (1.3); 7.0147 (0.6); 7.0089 (0.5); 6.8594 (0.8); 6.8539 (0.8); 6.8328 (1.3); 6.8108 (0.6); 6.8061 (0.6); 6.2520 (1.2); 5.3375 (1.7); 4.2123 (0.4); 4.1949 (2.0); 4.1707 (3.8); 4.1471 (2.7); 4.1233 (0.9); 3.9275 (1.0); 3.9116 (1.9); 3.8979 (0.7); 3.8858 (1.8); 3.8699 (0.6); 3.0176 (0.6); 3.0024 (0.7); 2.9730 (1.0); 2.9564 (1.0); 2.8715 (1.1); 2.8435 (1.0); 2.8272 (0.7); 2.7969 (0.6); 2.6782 (16.0); 2.1311 (0.5); 2.1200 (0.6); 2.1031 (1.0); 2.0830 (12.0); 2.0573 (0.4); 1.6042 (5.8); 1.3205 (3.2); 1.2967 (6.4); 1.2729 (3.0); 1.0830 (0.4); 1.0725 (1.8); 1.0654 (1.9); 1.0549 (1.0); 1.0504 (0.8); 1.0439 (1.8); 1.0370 (1.8); 1.0265 (0.7); 1.0225 (0.7); 0.8231 (1.0); 0.8076 (2.0); 0.8009 (1.9); 0.7911 (2.2); 0.7841 (1.4); 0.7736 (0.8); 0.1065 (5.0); 0.0476 (0.7); 0.0368 (23.6); 0.0276 (0.8); 0.0259 (0.9) I-296: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1563 (13.7); 8.0581 (8.1); 8.0292 (8.6); 7.6479 (0.8); 7.6279 (8.3); 7.6037 (3.6); 7.5776 (1.0); 7.4148 (8.2); 7.3860 (7.3); 7.3507 (4.1); 7.2984 (22.8); 7.2685 (1.8); 7.2616 (2.3); 7.2453 (1.7); 7.2383 (2.5); 7.2311 (1.2); 6.1043 (2.6); 5.3369 (13.6); 4.2139 (1.2); 4.2054 (2.6); 4.1792 (3.0); 4.1711 (1.9); 4.1012 (0.5); 4.0352 (0.3); 4.0177 (0.8); 4.0091 (1.2); 4.0006 (1.2); 3.9814 (4.1); 3.9622 (1.4); 3.9471 (2.9); 3.9316 (1.5); 3.1946 (1.2); 3.1772 (1.2); 3.1495 (2.6); 3.1319 (2.4); 3.0356 (2.1); 3.0232 (0.6); 3.0057 (2.1); 2.9907 (1.4); 2.9608 (1.4); 2.0816 (2.0); 2.0423 (0.7); 1.5903 (16.0); 1.3198 (0.4); 1.2960 (0.8); 0.9971 (0.4); 0.9727 (0.7); 0.1069 (4.0); 0.0478 (1.2); 0.0371 (27.6); 0.0263 (1.0) I-297: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1645 (7.0); 7.6614 (0.4); 7.6433 (4.4); 7.6217 (1.9); 7.5954 (0.5); 7.4913 (3.2); 7.4645 (4.1); 7.3898 (2.1); 7.2987 (13.7); 7.2920 (5.2); 7.2806 (1.5); 7.2646 (4.3); 7.2572 (1.8); 7.2491 (0.6); 6.1210 (1.5); 5.3374 (1.1); 4.2434 (1.3); 4.2176 (1.4); 4.2095 (0.8); 3.9682 (0.4); 3.9590 (0.6); 3.9512 (0.6); 3.9317 (2.0); 3.8990 (1.6); 3.8814 (0.8); 3.1077 (0.7); 3.0918 (0.7); 3.0628 (1.3); 3.0468 (1.2); 2.9039 (1.0); 2.8731 (1.0); 2.8592 (0.8); 2.8284 (0.7); 1.5842 (16.0); 0.1078 (1.9); 0.0489 (0.7); 0.0381 (16.4); 0.0289 (0.4); 0.0272 (0.5) I-298: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9606 (5.3); 7.4108 (0.7); 7.3969 (0.8); 7.3918 (1.1); 7.3796 (1.4); 7.3662 (1.0); 7.3567 (1.0); 7.2986 (8.2); 7.2219 (0.5); 7.2090 (0.4); 7.1949 (4.6); 7.1810 (2.4); 7.1794 (2.4); 7.1760 (2.1); 7.1711 (2.6); 7.1517 (0.4); 7.1030 (2.3); 7.0769 (2.6); 7.0430 (2.6); 7.0372 (2.6); 6.6897 (1.4); 6.6839 (1.4); 6.6635 (1.2); 6.6578 (1.2); 6.0532 (1.3); 4.2478 (0.9); 4.2369 (1.1); 4.2118 (1.2); 4.2006 (1.3); 4.0454 (0.4); 4.0355 (0.6); 4.0198 (0.6); 4.0149 (0.6); 4.0056 (0.6); 3.9964 (0.5); 3.9887 (0.4); 3.9221 (1.5); 3.9041 (1.1); 3.8860 (1.2); 3.8680 (0.9); 3.1863 (0.9); 3.1700 (0.9); 3.1415 (1.2); 3.1251 (1.2); 2.9248 (1.2); 2.8938 (1.2); 2.8799 (0.9); 2.8490 (0.9); 2.7434 (0.4); 2.6795 (16.0); 1.7928 (0.6); 1.7818 (0.6); 1.7651 (1.1); 1.7482 (0.6); 1.7372 (0.7); 1.7201 (0.3); 1.6034 (4.8); 0.9932 (0.4); 0.9765 (1.7); 0.9703 (2.1); 0.9668 (1.6); 0.9481 (1.9); 0.9423 (1.9); 0.9259 (0.5); 0.6030 (1.0); 0.5989 (1.0); 0.5936 (1.1); 0.5885 (1.7); 0.5822 (1.9); 0.5769 (1.7); 0.5659 (1.1); 0.5598 (0.9); 0.0484 (0.4); 0.0377 (10.8); 0.0285 (0.4); 0.0268 (0.4) I-299: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9665 (4.0); 7.4121 (0.5); 7.4043 (0.6); 7.3869 (1.0); 7.3794 (0.7); 7.3641 (0.8); 7.3579 (0.7); 7.2986 (19.5); 7.2144 (0.5); 7.2099 (0.4); 7.1869 (1.3); 7.1825 (1.2); 7.1576 (2.1); 7.1499 (1.1); 7.1364 (1.0); 7.1303 (1.1); 7.1089 (0.4); 7.1028 (0.4); 7.0197 (1.5); 6.9937 (1.6); 6.8312 (1.7); 6.6202 (0.9); 6.6141 (0.9); 6.5939 (0.8); 6.0979 (1.1); 4.2992 (0.6); 4.2911 (0.8); 4.2660 (0.9); 4.2567 (0.7); 4.1728 (0.4); 4.1489 (0.4); 3.9000 (0.5); 3.8840 (0.5); 3.8764 (0.5); 3.8639 (1.5); 3.8439 (0.4); 3.8303 (1.1); 3.8096 (0.6); 3.0387 (0.6); 3.0236 (0.5); 2.9938 (0.8); 2.9778 (0.8); 2.7776 (0.7); 2.7460 (0.8); 2.7320 (0.7); 2.7002 (0.6); 2.6755 (12.4); 2.3519 (0.5); 2.3107 (9.2); 2.0830 (2.2); 1.7686 (0.4); 1.7575 (0.4); 1.7409 (0.8); 1.7236 (0.5); 1.7126 (0.5); 1.5803 (16.0); 1.3217 (0.5); 1.2979 (1.2); 1.2741 (0.5); 0.9428 (0.4); 0.9367 (0.4); 0.9277 (1.3); 0.9213 (1.6); 0.9064 (0.6); 0.8994 (1.4); 0.8933 (1.4); 0.8784 (0.4); 0.5831 (0.7); 0.5736 (0.8); 0.5683 (1.5); 0.5605 (1.5); 0.5520 (1.7); 0.5447 (0.9); 0.5357 (0.6); 0.0496 (1.0); 0.0389 (27.7); 0.0297 (0.9); 0.0281 (1.1) I-300: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9619 (5.3); 7.4224 (0.6); 7.4162 (0.7); 7.4008 (0.8); 7.3956 (1.4); 7.3898 (1.0); 7.3738 (1.0); 7.3681 (0.9); 7.2989 (12.5); 7.2554 (1.9); 7.2500 (2.1); 7.2383 (0.9); 7.2331 (0.8); 7.2109 (1.6); 7.2059 (1.6); 7.1836 (1.1); 7.1792 (1.2); 7.1581 (1.2); 7.1520 (1.3); 7.1361 (1.1); 7.1306 (1.5); 7.1246 (0.6); 7.1088 (0.7); 7.1030 (0.6); 7.0943 (0.8); 7.0880 (0.8); 7.0673 (1.5); 7.0609 (1.5); 7.0220 (2.9); 6.9950 (1.3); 6.0635 (1.2); 5.3373 (1.8); 4.2396 (1.1); 4.2141 (1.2); 4.1955 (0.4); 3.9344 (0.4); 3.9248 (0.6); 3.9168 (0.8); 3.9088 (1.4); 3.9032 (1.7); 3.8951 (1.0); 3.8868 (0.6); 3.8764 (1.7); 3.8582 (0.7); 3.0260 (0.7); 3.0103 (0.7); 2.9806 (1.0); 2.9644 (1.0); 2.8541 (1.0); 2.8239 (0.9); 2.8091 (0.7); 2.7778 (0.6); 2.7021 (0.6); 2.6834 (16.0); 2.3519 (0.6); 2.3299 (11.7); 2.0825 (0.6); 1.5902 (5.6); 1.2974 (0.4); 0.0495 (0.6); 0.0385 (17.2); 0.0278 (0.7) I-301: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9548 (4.4); 7.2989 (10.6); 7.1469 (2.1); 7.1186 (2.5); 7.0873 (2.2); 7.0780 (1.2); 7.0630 (0.9); 7.0570 (1.0); 7.0362 (0.4); 7.0299 (0.3); 6.9005 (2.2); 6.8918 (2.3); 6.8600 (0.6); 6.8522 (0.6); 6.8371 (1.0); 6.8311 (0.8); 6.8127 (0.5); 6.8065 (0.5); 6.5032 (1.3); 6.4945 (1.2); 6.4751 (1.2); 6.4664 (1.1); 6.2321 (1.0); 4.2297 (0.8); 4.2187 (0.8); 4.1937 (1.0); 4.1827 (1.0); 4.0275 (0.3); 4.0171 (0.5); 4.0074 (0.5); 3.9977 (0.5); 3.9890 (0.5); 3.9794 (0.4); 3.9183 (1.2); 3.9005 (0.9); 3.8823 (1.0); 3.8645 (0.8); 3.6949 (16.0); 3.1682 (0.7); 3.1512 (0.7); 3.1230 (1.0); 3.1060 (0.9); 2.9230 (1.0); 2.8930 (1.0); 2.8778 (0.7); 2.8477 (0.7); 2.6747 (13.6); 2.1345 (0.4); 2.1237 (0.4); 2.1068 (0.8); 2.0893 (0.5); 2.0829 (0.9); 1.5976 (7.9); 1.3442 (0.4); 1.3208 (0.8); 1.3051 (2.3); 1.2975 (2.1); 1.2734 (0.3); 1.0793 (0.5); 1.0658 (1.3); 1.0586 (1.6); 1.0549 (1.0); 1.0510 (0.8); 1.0453 (0.9); 1.0369 (1.4); 1.0304 (1.4); 1.0170 (0.7); 0.9418 (0.8); 0.9200 (2.6); 0.8968 (1.0); 0.8212 (0.8); 0.8126 (0.8); 0.8075 (1.5); 0.8040 (1.6); 0.7994 (1.4); 0.7903 (1.6); 0.7873 (1.5); 0.7823 (1.2); 0.7704 (0.6); 0.1076 (5.3); 0.0486 (0.6); 0.0379 (15.2); 0.0269 (0.6) I-302: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9580 (5.1); 7.4077 (0.7); 7.3956 (0.8); 7.3867 (1.3); 7.3751 (1.5); 7.3644 (0.9); 7.3534 (1.0); 7.2989 (12.0); 7.2202 (0.4); 7.2113 (0.4); 7.1954 (3.8); 7.1832 (2.1); 7.1742 (1.9); 7.1709 (3.1); 7.1497 (2.3); 7.1469 (2.3); 7.1356 (0.5); 7.1052 (2.1); 7.0796 (2.4); 6.7903 (1.1); 6.7647 (0.9); 6.0392 (1.0); 4.2576 (0.8); 4.2467 (1.0); 4.2215 (1.1); 4.2104 (1.2); 4.1950 (0.5); 4.1711 (1.3); 4.1473 (1.4); 4.1236 (0.5); 4.0681 (0.4); 4.0584 (0.5); 4.0498 (0.5); 4.0428 (0.5); 4.0372 (0.5); 4.0285 (0.5); 4.0196 (0.4); 3.9240 (1.4); 3.9059 (1.1); 3.8879 (1.2); 3.8697 (1.0); 3.1951 (0.7); 3.1786 (0.7); 3.1505 (1.0); 3.1336 (1.0); 2.9379 (1.2); 2.9070 (1.1); 2.8930 (0.9); 2.8621 (0.8); 2.6796 (16.0); 2.6684 (0.8); 2.5492 (1.7); 2.3907 (1.2); 2.2241 (10.3); 2.0826 (6.4); 1.6144 (4.4); 1.4694 (2.0); 1.3204 (1.7); 1.2967 (3.5); 1.2729 (1.6); 0.1072 (3.6); 0.0480 (0.5); 0.0462 (0.3); 0.0446 (0.4); 0.0372 (15.8); 0.0294 (0.4); 0.0278 (0.4); 0.0263 (0.6) I-303: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9489 (4.9); 7.4000 (0.6); 7.3924 (0.7); 7.3746 (1.2); 7.3672 (0.9); 7.3518 (0.9); 7.3458 (0.8); 7.2988 (9.5); 7.2015 (0.7); 7.1970 (0.5); 7.1741 (1.6); 7.1696 (1.4); 7.1441 (2.2); 7.1354 (1.3); 7.1217 (1.1); 7.1156 (1.4); 7.0942 (0.6); 7.0882 (0.4); 6.9785 (2.4); 6.9464 (0.4); 6.9131 (4.3); 6.8861 (0.4); 6.0956 (1.3); 4.3239 (0.8); 4.3125 (0.9); 4.2878 (1.0); 4.2765 (1.1); 3.9428 (0.4); 3.9266 (0.6); 3.9208 (0.5); 3.9107 (0.6); 3.8991 (0.4); 3.8948 (0.4); 3.8309 (1.6); 3.8091 (1.0); 3.7950 (1.3); 3.7733 (0.9); 3.0175 (0.7); 3.0009 (0.7); 2.9725 (1.0); 2.9563 (0.9); 2.6893 (1.2); 2.6685 (15.3); 2.6577 (1.8); 2.6446 (1.0); 2.6121 (0.8); 2.1437 (11.4); 2.1273 (11.4); 1.6113 (16.0); 1.3042 (1.3); 0.9412 (0.4); 0.9193 (1.4); 0.8963 (0.5); 0.1071 (0.6); 0.0480 (0.4); 0.0372 (12.3); 0.0280 (0.4); 0.0263 (0.5) I-304: ¹H-NMR(300.1 MHz, d₆-DMSO): δ = 8.1840 (16.0); 8.1689 (3.0); 7.7574 (4.4); 7.7351 (2.8); 7.7093 (3.6); 7.6889 (3.7); 7.6640 (3.4); 7.6589 (3.6); 7.6328 (1.6); 7.6014 (6.5); 7.5944 (7.0); 7.5205 (4.1); 7.4925 (6.2); 7.3910 (3.8); 7.3840 (3.6); 7.3630 (2.5); 7.3560 (2.5); 4.8376 (1.3); 4.8240 (1.6); 4.8134 (1.6); 4.7983 (1.3); 3.4683 (0.6); 3.4543 (0.8); 3.4383 (0.8); 3.4231 (1.5); 3.4098 (1.2); 3.3939 (1.4); 3.3799 (1.3); 3.3176 (1.0); 3.2839 (1.4); 3.2673 (2.2); 3.2497 (1.3); 3.2403 (1.0); 3.2221 (1.3); 3.2037 (0.7); 2.7339 (0.5); 2.7277 (0.6); 2.7216 (0.4); 2.5135 (41.2); 2.5075 (81.7); 2.5015 (109.2); 2.4956 (75.8); 2.4898 (35.2); 2.2776 (0.5); 2.2715 (0.7); 2.2650 (0.5); 2.1469 (0.9); 2.1308 (1.0); 2.1169 (0.8); 2.1023 (1.1); 2.0872 (1.0); 1.5063 (0.6); 1.4897 (0.9); 1.4753 (0.7); 1.4624 (0.8); 1.4483 (0.6); 0.0108 (0.9); −0.0002 (24.7); −0.0112 (0.8) I-305: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9502 (5.3); 7.5550 (0.7); 7.5288 (1.8); 7.5026 (1.4); 7.4525 (1.6); 7.4269 (0.9); 7.2983 (0.9); 7.2431 (1.9); 7.2420 (1.9); 7.1687 (1.0); 7.1655 (1.2); 7.1617 (1.0); 7.1421 (0.9); 7.1387 (1.0); 7.1349 (0.9); 6.9671 (2.7); 6.9048 (6.6); 6.9021 (6.4); 6.8746 (1.2); 6.6867 (2.4); 6.4989 (1.2); 6.2326 (1.6); 4.2939 (0.9); 4.2825 (1.0); 4.2581 (1.1); 4.2466 (1.1); 3.9168 (0.4); 3.9044 (0.6); 3.9006 (0.6); 3.8945 (0.6); 3.8885 (0.6); 3.8844 (0.6); 3.8727 (0.5); 3.8684 (0.4); 3.8058 (1.6); 3.7840 (1.0); 3.7700 (1.4); 3.7482 (1.0); 2.9972 (0.8); 2.9813 (0.8); 2.9524 (1.0); 2.9363 (1.0); 2.6693 (1.6); 2.6564 (16.0); 2.6377 (1.3); 2.6250 (1.0); 2.5926 (1.0); 2.1976 (0.6); 2.1477 (12.1); 2.1083 (12.2); 0.0364 (1.1) I-306: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9665 (5.4); 7.5785 (0.7); 7.5524 (1.7); 7.5260 (1.3); 7.4733 (1.6); 7.4476 (0.9); 7.2991 (2.0); 7.2695 (1.9); 7.1881 (1.1); 7.1843 (1.0); 7.1646 (0.8); 7.1613 (1.0); 7.1575 (0.9); 7.0038 (2.0); 6.9778 (2.3); 6.8966 (1.2); 6.8359 (2.2); 6.8318 (2.3); 6.7087 (2.4); 6.6111 (1.3); 6.6054 (1.2); 6.5852 (1.1); 6.5796 (1.1); 6.5209 (1.2); 6.2074 (1.5); 4.2824 (0.8); 4.2733 (1.0); 4.2480 (1.1); 4.2392 (1.0); 3.9022 (0.4); 3.8909 (0.5); 3.8860 (0.6); 3.8805 (0.5); 3.8764 (0.6); 3.8702 (0.6); 3.8618 (0.5); 3.8464 (2.1); 3.8261 (0.6); 3.8121 (1.4); 3.7914 (0.8); 3.0270 (0.8); 3.0126 (0.7); 2.9820 (1.1); 2.9666 (1.1); 2.7564 (1.0); 2.7249 (1.0); 2.7109 (1.0); 2.6695 (16.0); 2.2956 (12.3); 2.0361 (4.9); 1.8012 (0.4); 1.7843 (0.7); 1.7731 (0.7); 1.7563 (1.2); 1.7447 (0.5); 1.7395 (0.8); 1.7284 (0.7); 1.7114 (0.4); 0.9571 (0.4); 0.9405 (2.0); 0.9341 (2.2); 0.9175 (1.0); 0.9123 (2.1); 0.9058 (2.0); 0.8899 (0.5); 0.5917 (0.8); 0.5848 (1.2); 0.5749 (1.6); 0.5681 (2.2); 0.5617 (1.7); 0.5514 (1.3); 0.5449 (0.9); 0.0371 (2.6) I-307: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1461 (16.0); 8.0469 (8.1); 8.0395 (7.9); 7.8515 (1.8); 7.6487 (12.2); 7.6322 (15.1); 7.5876 (6.0); 7.5794 (5.5); 7.5600 (6.2); 7.5519 (5.9); 7.5216 (1.4); 7.4683 (9.9); 7.4500 (7.0); 7.4113 (4.1); 7.3974 (5.2); 7.3919 (4.7); 7.3821 (3.8); 7.2988 (13.2); 7.2496 (0.4); 7.2321 (0.4); 7.1681 (7.9); 7.1407 (6.8); 5.3362 (0.7); 4.3141 (3.8); 4.3029 (4.3); 4.2780 (4.4); 4.2667 (4.9); 4.1729 (3.1); 4.1664 (3.3); 4.1601 (3.4); 3.9018 (4.9); 3.8818 (4.4); 3.8653 (4.3); 3.8457 (3.6); 3.0635 (14.2); 3.0418 (10.3); 2.9887 (0.7); 2.6570 (0.7); 2.3408 (0.3); 2.1482 (0.4); 2.0817 (0.5); 1.6317 (3.1); 1.2908 (3.5); 0.9162 (0.5); 0.8926 (0.4); 0.1066 (5.1); 0.0357 (15.8) I-308: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.0500 (16.0); 8.0146 (1.1); 7.4739 (0.5); 7.4474 (3.7); 7.4334 (6.2); 7.4204 (4.4); 7.3921 (1.1); 7.3812 (0.9); 7.3666 (0.8); 7.3061 (12.1); 7.2705 (2.8); 7.2364 (3.5); 7.2208 (6.8); 7.2066 (6.0); 7.1920 (7.3); 7.1764 (8.3); 7.1603 (3.8); 7.1359 (8.5); 7.1197 (9.8); 7.0533 (0.7); 7.0284 (0.7); 7.0093 (0.7); 6.9756 (7.2); 6.9593 (6.1); 6.9125 (0.5); 6.0321 (7.2); 4.1085 (4.3); 4.1038 (4.8); 4.0867 (5.4); 4.0819 (5.7); 3.9862 (4.0); 3.9790 (4.5); 3.9719 (4.3); 3.9129 (5.7); 3.9039 (4.8); 3.8910 (4.8); 3.8821 (4.0); 3.4250 (0.4); 3.3750 (15.2); 3.3306 (0.8); 3.1269 (3.7); 3.1163 (3.9); 3.0998 (5.1); 3.0891 (4.9); 3.0623 (0.9); 3.0487 (0.9); 3.0235 (0.5); 2.9675 (4.8); 2.9496 (5.0); 2.9406 (4.1); 2.9226 (3.6); 1.9907 (4.5); −0.0002 (1.7) I-309: ¹H-NMR(499.9 MHz, d₆-DMSO): δ = 7.7226 (7.6); 7.3443 (2.5); 7.3381 (2.6); 7.2808 (3.8); 7.2204 (3.7); 7.1631 (0.4); 7.1473 (4.6); 7.1365 (4.2); 7.1206 (0.8); 7.0632 (3.9); 6.9126 (0.9); 6.9005 (1.5); 6.8939 (1.6); 6.8856 (1.1); 6.8806 (0.9); 5.7547 (0.4); 3.8020 (2.7); 3.7925 (1.5); 3.7849 (3.3); 3.7797 (2.0); 3.7219 (1.4); 3.7118 (1.8); 3.6984 (1.4); 3.6889 (0.8); 3.3456 (65.7); 2.8019 (4.0); 2.7887 (4.0); 2.5729 (19.2); 2.5084 (1.9); 2.5051 (2.5); 2.5018 (2.0); 2.1733 (16.0); 2.0870 (0.4); 2.0766 (0.8); 2.0700 (0.9); 2.0599 (1.6); 2.0497 (1.0); 2.0433 (1.0); 2.0328 (0.5); 1.0323 (0.9); 1.0239 (2.8); 1.0196 (3.0); 1.0117 (1.8); 1.0071 (2.9); 1.0028 (3.0); 0.9951 (1.3); 0.7839 (1.1); 0.7756 (3.0); 0.7723 (3.4); 0.7656 (3.4); 0.7620 (3.3); 0.7534 (1.2) I-310: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1605 (9.8); 7.6440 (0.4); 7.6300 (4.8); 7.6126 (4.8); 7.3922 (2.6); 7.3425 (1.1); 7.3343 (1.1); 7.3257 (1.7); 7.3193 (1.4); 7.3123 (1.1); 7.2989 (13.0); 6.7089 (5.3); 6.2273 (2.0); 4.3514 (1.2); 4.3421 (1.4); 4.3159 (1.5); 4.3062 (1.5); 3.9054 (0.6); 3.8994 (0.6); 3.8933 (0.8); 3.8898 (0.8); 3.8782 (0.7); 3.8719 (0.9); 3.8657 (0.6); 3.8558 (0.6); 3.8145 (2.6); 3.7926 (1.4); 3.7789 (2.0); 3.7571 (1.4); 2.9493 (1.0); 2.9342 (1.0); 2.9020 (1.5); 2.8876 (1.4); 2.7077 (1.7); 2.6744 (1.6); 2.6607 (1.2); 2.6272 (1.2); 2.2636 (16.0); 2.0705 (16.0); 2.0459 (1.1); 1.6052 (2.2); 1.2919 (1.6); 1.2686 (0.3); 1.2437 (0.4); 0.9172 (0.3); 0.8931 (0.3); 0.1072 (5.6); 0.0480 (0.5); 0.0372 (15.5); 0.0263 (0.6) I-311: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9678 (6.9); 7.6456 (0.5); 7.6203 (1.5); 7.5964 (4.4); 7.5730 (1.1); 7.5483 (3.6); 7.5120 (1.4); 7.4881 (1.4); 7.4814 (1.8); 7.4737 (1.0); 7.4448 (1.7); 7.3255 (1.3); 7.2986 (16.8); 7.2774 (3.1); 7.2417 (2.2); 7.2254 (0.8); 7.2180 (1.8); 7.1928 (0.7); 7.1753 (2.5); 7.1630 (3.4); 7.1539 (3.6); 7.1411 (0.6); 7.0967 (2.8); 7.0922 (3.4); 7.0687 (2.7); 7.0106 (1.7); 6.9987 (1.8); 6.9864 (1.4); 6.9788 (1.2); 6.2992 (1.2); 6.1797 (1.6); 5.3375 (6.1); 4.3859 (0.8); 4.3718 (1.0); 4.3646 (1.1); 4.3506 (1.7); 4.3350 (1.1); 4.3283 (1.3); 4.3157 (1.2); 3.8838 (1.3); 3.8614 (1.5); 3.8467 (1.6); 3.8246 (1.5); 3.8197 (1.3); 3.8064 (0.9); 3.7827 (0.9); 3.2524 (0.4); 3.2403 (0.5); 3.2320 (0.7); 3.2233 (0.8); 3.2169 (0.8); 3.2107 (0.8); 3.2032 (1.0); 3.1949 (0.8); 3.1888 (0.8); 3.1821 (0.8); 3.1722 (0.6); 3.1665 (0.6); 3.1594 (0.6); 3.1439 (0.4); 2.7134 (16.0); 2.6948 (12.0); 2.0413 (0.4); 2.0250 (0.8); 2.0112 (1.2); 1.9957 (1.4); 1.9890 (1.2); 1.9740 (1.1); 1.9494 (0.6); 1.6069 (15.5); 1.3811 (0.4); 1.3550 (0.8); 1.3429 (1.0); 1.3343 (1.0); 1.3194 (1.1); 1.3136 (1.1); 1.3044 (1.2); 1.2912 (1.6); 1.2733 (0.9); 1.2579 (0.7); 1.2460 (0.5); 1.2275 (0.4); 1.1667 (0.5); 1.1484 (1.2); 1.1391 (0.6); 1.1302 (1.0); 1.1181 (3.1); 1.0938 (3.7); 1.0830 (1.5); 1.0709 (2.8); 1.0532 (1.1); 1.0352 (0.4); 0.1073 (5.4); 0.0373 (19.3) I-312: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.0976 (8.0); 7.5320 (0.9); 7.5280 (1.1); 7.5200 (1.0); 7.5168 (1.3); 7.5129 (1.9); 7.5076 (1.1); 7.5006 (1.1); 7.2591 (2.3); 7.1452 (0.4); 7.1411 (0.6); 7.1289 (1.9); 7.1247 (1.8); 7.1197 (5.4); 7.1127 (2.0); 7.1057 (2.6); 7.0888 (0.8); 6.9547 (2.6); 6.9394 (3.0); 6.8670 (3.2); 6.6759 (1.7); 6.6608 (1.6); 6.0109 (2.1); 5.2946 (2.3); 4.2771 (1.3); 4.2706 (1.4); 4.2556 (1.5); 4.2491 (1.6); 3.8791 (0.6); 3.8750 (0.7); 3.8690 (0.9); 3.8655 (0.8); 3.8592 (0.9); 3.8559 (0.8); 3.8528 (0.7); 3.8495 (0.8); 3.8394 (0.4); 3.8130 (2.1); 3.8005 (1.4); 3.7914 (1.9); 3.7789 (1.4); 3.0015 (1.1); 2.9917 (1.2); 2.9742 (1.4); 2.9643 (1.4); 2.7125 (1.5); 2.6927 (1.5); 2.6852 (1.4); 2.6654 (1.3); 2.2639 (16.0); 2.1413 (15.2); 1.5976 (1.5); −0.0002 (2.1) I-314: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.6449 (0.4); 7.3843 (0.4); 7.3651 (0.7); 7.3292 (20.9); 7.3164 (16.8); 7.3106 (18.7); 7.2988 (76.8); 7.2836 (0.8); 7.2440 (0.6); 7.2323 (0.4); 7.2103 (0.4); 7.1809 (0.4); 7.1491 (10.3); 7.1447 (9.8); 7.1208 (7.4); 7.1165 (7.2); 6.9477 (0.4); 5.3371 (0.7); 3.7565 (1.4); 3.7361 (2.6); 3.7155 (1.3); 3.7000 (11.0); 3.6872 (11.9); 3.6647 (14.7); 3.6520 (15.6); 3.6280 (2.2); 3.6063 (1.1); 3.4614 (13.0); 3.4384 (16.0); 3.4261 (10.0); 3.4032 (12.6); 3.2783 (3.3); 3.2653 (3.6); 3.2596 (4.7); 3.2510 (5.5); 3.2469 (5.3); 3.2377 (6.9); 3.2325 (5.7); 3.2282 (5.0); 3.2238 (4.7); 3.2196 (5.4); 3.2096 (4.0); 3.1967 (3.3); 3.1585 (0.3); 2.9942 (10.0); 2.9755 (8.7); 2.9490 (14.1); 2.9304 (12.6); 2.8250 (0.3); 2.7615 (14.2); 2.7343 (12.9); 2.7164 (10.1); 2.6891 (8.9); 2.6244 (0.4); 2.3395 (0.3); 2.3172 (0.3); 2.2785 (0.3); 2.2381 (0.4); 2.0560 (0.6); 2.0391 (0.6); 1.9759 (0.7); 1.9495 (1.0); 1.9298 (1.2); 1.9008 (1.2); 1.8807 (1.1); 1.8269 (1.1); 1.8050 (1.3); 1.7866 (1.8); 1.7578 (1.9); 1.7483 (2.0); 1.7285 (2.8); 1.7171 (2.4); 1.7093 (2.3); 1.5696 (3.5); 1.3838 (1.4); 1.3224 (1.2); 1.2932 (1.8); 1.2571 (0.8); 1.2271 (0.8); 1.0531 (0.4); 1.0099 (0.5); 0.9171 (0.4); 0.8904 (0.4); 0.2034 (0.6); 0.1925 (20.0); 0.1817 (0.8); 0.1651 (1.6); 0.1063 (5.6); 0.0473 (2.6); 0.0442 (1.7); 0.0366 (84.4); 0.0273 (3.2); 0.0257 (3.6); 0.0024 (0.4); −0.0299 (0.5); −0.1621 (0.4) I-315: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9471 (5.3); 7.2988 (8.3); 7.2705 (2.2); 7.1365 (0.6); 7.1015 (2.2); 7.0754 (2.5); 7.0524 (1.0); 7.0463 (1.1); 7.0285 (1.1); 7.0238 (1.3); 7.0021 (0.6); 6.9964 (0.5); 6.8548 (0.9); 6.8479 (1.8); 6.8284 (1.4); 6.8228 (1.5); 6.8079 (0.8); 6.8021 (0.6); 6.2214 (1.4); 5.3375 (0.5); 4.2693 (0.9); 4.2580 (1.0); 4.2331 (1.1); 4.2218 (1.2); 4.0819 (0.4); 4.0711 (0.6); 4.0640 (0.6); 4.0517 (0.6); 4.0446 (0.6); 4.0344 (0.5); 3.8907 (1.4); 3.8712 (1.2); 3.8545 (1.2); 3.8350 (1.0); 3.2652 (5.4); 3.2514 (0.9); 3.2346 (0.8); 3.2072 (1.1); 3.1906 (1.0); 2.9531 (1.1); 2.9226 (1.1); 2.9092 (0.9); 2.8788 (0.9); 2.6677 (16.0); 2.2034 (11.3); 2.1406 (0.5); 2.1294 (0.6); 2.1124 (1.0); 2.0953 (0.6); 2.0843 (0.6); 1.6122 (5.9); 1.0880 (0.7); 1.0748 (1.5); 1.0680 (1.8); 1.0599 (1.0); 1.0553 (1.1); 1.0462 (1.6); 1.0398 (1.7); 1.0269 (0.8); 0.8298 (0.9); 0.8226 (0.9); 0.8135 (1.9); 0.8067 (1.7); 0.7980 (2.0); 0.7908 (1.2); 0.7806 (0.6); 0.1187 (0.6); 0.1067 (15.2); 0.0944 (0.6); 0.0473 (0.5); 0.0367 (11.7); 0.0258 (0.5) I-316: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9734 (5.2); 7.5974 (0.4); 7.5796 (0.9); 7.5676 (0.8); 7.5535 (0.5); 7.5494 (0.5); 7.5457 (0.5); 7.3494 (3.7); 7.3315 (2.3); 7.3252 (1.8); 7.2988 (2.9); 7.0973 (1.1); 7.0163 (1.7); 6.9908 (2.0); 6.9146 (2.6); 6.9036 (2.1); 6.7321 (1.2); 6.7172 (1.1); 6.6917 (1.0); 6.1098 (1.3); 4.3139 (0.8); 4.3044 (0.9); 4.2792 (1.0); 4.2694 (1.0); 3.9352 (0.4); 3.9283 (0.4); 3.9230 (0.5); 3.9183 (0.5); 3.9124 (0.5); 3.9074 (0.5); 3.9020 (0.6); 3.8960 (0.4); 3.8862 (0.5); 3.8783 (0.5); 3.8685 (1.8); 3.8479 (0.7); 3.8336 (1.4); 3.8129 (0.9); 3.0490 (0.7); 3.0335 (0.7); 3.0040 (1.0); 2.9879 (0.9); 2.7831 (1.1); 2.7518 (1.0); 2.7384 (1.3); 2.7061 (0.8); 2.6721 (16.0); 2.3053 (11.2); 2.2878 (0.4); 2.1571 (10.5); 0.0372 (3.8) I-317: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9610 (4.9); 7.5909 (0.4); 7.5753 (0.8); 7.5624 (0.7); 7.5464 (0.5); 7.5427 (0.5); 7.3690 (0.4); 7.3415 (2.7); 7.3237 (2.5); 7.3184 (1.9); 7.3109 (1.1); 7.2986 (3.0); 7.0888 (1.0); 6.9818 (2.1); 6.9434 (0.6); 6.9175 (1.9); 6.9120 (2.1); 6.9060 (3.0); 6.9007 (3.0); 6.8748 (0.7); 6.7237 (1.1); 6.1214 (1.2); 4.3159 (0.8); 4.3063 (0.9); 4.2802 (0.9); 4.2703 (1.0); 3.9378 (0.4); 3.9314 (0.4); 3.9261 (0.5); 3.9213 (0.5); 3.9155 (0.5); 3.9099 (0.5); 3.9054 (0.5); 3.9000 (0.4); 3.8942 (0.4); 3.8890 (0.4); 3.8349 (1.6); 3.8133 (0.9); 3.7991 (1.3); 3.7776 (0.9); 3.0137 (0.7); 2.9975 (0.7); 2.9689 (0.9); 2.9526 (0.8); 2.6994 (1.1); 2.6679 (16.0); 2.6553 (1.3); 2.6225 (0.8); 2.1207 (10.7); 2.1135 (11.0); 0.0372 (3.7) I-318: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9778 (4.9); 7.6071 (0.7); 7.5825 (2.3); 7.5599 (5.6); 7.5205 (3.1); 7.4593 (2.0); 7.4369 (1.3); 7.2993 (4.8); 6.9232 (3.7); 6.9049 (1.7); 6.8772 (4.4); 6.8596 (3.2); 6.8320 (1.0); 6.8271 (0.9); 6.1626 (2.5); 4.7046 (1.2); 4.6832 (1.4); 4.6695 (1.2); 4.3650 (1.6); 4.3520 (1.6); 4.3285 (1.9); 4.3156 (1.9); 4.2709 (16.0); 4.1919 (0.8); 4.1683 (1.8); 4.1445 (1.8); 4.1204 (0.7); 3.7407 (1.5); 3.7155 (1.6); 3.7038 (1.5); 3.6787 (1.3); 2.7262 (15.1); 2.0810 (6.7); 1.6349 (1.9); 1.3191 (2.5); 1.2951 (5.4); 1.2716 (2.3); 0.9166 (0.4); 0.1071 (2.8); 0.0363 (5.8) I-319: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.2201 (0.7); 8.1037 (16.0); 8.1028 (15.8); 7.8124 (0.7); 7.4671 (0.5); 7.4574 (2.7); 7.4530 (2.8); 7.4417 (6.0); 7.4375 (5.9); 7.4260 (3.9); 7.4218 (3.6); 7.4096 (0.8); 7.3918 (0.8); 7.3751 (0.4); 7.3649 (0.5); 7.3485 (0.4); 7.3152 (6.9); 7.3103 (9.7); 7.3053 (6.4); 7.2801 (4.1); 7.2606 (42.6); 7.2295 (0.5); 7.2257 (0.6); 7.2031 (0.5); 7.1867 (0.5); 7.1826 (0.4); 7.1739 (0.5); 7.1623 (0.4); 7.1435 (0.4); 7.1278 (0.4); 7.1073 (8.9); 7.0909 (10.3); 7.0488 (0.4); 7.0093 (2.5); 7.0048 (3.1); 6.9990 (3.0); 6.9947 (4.6); 6.9899 (3.3); 6.9735 (10.0); 6.9252 (3.3); 6.9211 (3.2); 6.9088 (3.0); 6.9044 (3.4); 6.9012 (3.9); 6.8970 (3.4); 6.8847 (3.0); 6.8807 (2.8); 6.1420 (5.4); 5.7650 (0.5); 5.0348 (0.6); 4.1525 (2.6); 4.1468 (4.5); 4.1412 (2.8); 4.1307 (3.3); 4.1250 (5.4); 4.1194 (3.2); 3.9801 (3.0); 3.9719 (3.4); 3.9650 (3.1); 3.9108 (7.1); 3.9068 (9.4); 3.9023 (9.8); 3.8986 (9.1); 3.8898 (4.0); 3.8860 (3.7); 3.8801 (2.9); 3.8764 (2.7); 3.3633 (0.3); 3.1808 (3.7); 3.1779 (3.9); 3.1699 (7.3); 3.1618 (4.6); 3.1590 (4.2); 3.1364 (3.4); 3.1264 (3.4); 3.1093 (4.4); 3.0992 (4.3); 2.9481 (2.6); 2.9380 (2.9); 2.9299 (2.8); 2.9202 (4.2); 2.9109 (2.3); 2.9028 (2.1); 2.8926 (2.0); 2.7911 (3.6); 2.7859 (6.6); 2.7805 (6.8); 2.7750 (6.4); 2.7698 (3.6); 1.5551 (24.7); 1.2551 (1.3); 0.8818 (0.3); 0.0695 (0.5); −0.0002 (52.8) I-320: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.5913 (1.2); 7.5685 (3.5); 7.5462 (0.4); 7.4871 (1.8); 7.4617 (0.8); 7.4538 (1.2); 7.4465 (0.7); 7.4413 (0.5); 7.4381 (0.5); 7.4319 (0.7); 7.2991 (5.5); 7.0809 (1.3); 7.0553 (2.2); 7.0311 (2.0); 6.9805 (1.2); 6.9557 (0.7); 5.2802 (1.2); 4.1627 (0.9); 4.1371 (1.1); 4.1205 (0.4); 3.9665 (0.7); 3.9504 (1.5); 3.9365 (0.6); 3.9226 (1.5); 3.9007 (0.5); 3.6408 (0.9); 3.6252 (1.7); 3.6198 (1.4); 3.6112 (1.3); 3.6046 (1.7); 3.5907 (1.2); 3.4632 (0.4); 3.4488 (0.4); 3.4416 (0.3); 3.4268 (0.3); 3.4169 (0.9); 3.4019 (1.0); 3.3955 (0.9); 3.3806 (0.7); 3.3565 (0.8); 3.3395 (0.9); 3.3360 (1.0); 3.3192 (0.7); 3.3103 (0.4); 3.2939 (0.4); 3.2891 (0.4); 3.1594 (16.0); 3.1408 (0.4); 2.9716 (1.2); 2.9537 (1.9); 2.9272 (0.9); 2.3703 (0.4); 2.3364 (9.9); 2.3183 (9.3); 1.6290 (1.4); 0.1080 (1.3); 0.0376 (5.9) I-321: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1345 (10.4); 7.5040 (0.9); 7.4924 (1.0); 7.4836 (1.9); 7.4724 (2.0); 7.4633 (1.0); 7.4520 (1.2); 7.2989 (3.0); 7.2393 (0.4); 7.2335 (0.4); 7.2169 (4.7); 7.2122 (2.7); 7.2059 (2.4); 7.2030 (2.6); 7.1960 (2.4); 7.1916 (4.4); 7.1755 (0.4); 7.1689 (0.3); 7.0008 (2.5); 6.9753 (3.0); 6.9004 (2.8); 6.7174 (1.5); 6.6920 (1.3); 6.0870 (1.8); 4.3209 (1.1); 4.3119 (1.3); 4.2856 (1.4); 4.2768 (1.4); 3.9253 (0.5); 3.9185 (0.6); 3.9133 (0.7); 3.9083 (0.8); 3.9023 (0.7); 3.8975 (0.7); 3.8921 (0.8); 3.8862 (0.6); 3.8829 (0.6); 3.8762 (0.7); 3.8677 (0.7); 3.8582 (2.6); 3.8376 (1.0); 3.8234 (2.0); 3.8026 (1.3); 3.4046 (5.8); 3.0518 (1.0); 3.0362 (1.0); 3.0068 (1.4); 2.9904 (1.3); 2.7657 (1.4); 2.7341 (1.4); 2.7207 (1.2); 2.6885 (1.1); 2.3518 (0.5); 2.3328 (0.5); 2.3014 (16.0); 2.2059 (0.4); 2.1794 (15.0); 2.0394 (7.0); 1.6666 (0.5); 0.0378 (4.0) I-322: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.9095 (5.3); 7.2604 (13.4); 7.2106 (2.7); 7.1075 (0.7); 7.0916 (1.8); 7.0756 (1.1); 7.0050 (0.6); 7.0016 (0.5); 6.9856 (3.1); 6.9774 (4.6); 6.9607 (1.6); 6.8269 (0.8); 6.8136 (1.5); 6.8002 (0.8); 6.7979 (0.8); 6.1901 (1.6); 4.1964 (0.4); 4.1854 (1.3); 4.1703 (1.4); 4.1592 (0.5); 3.8680 (0.4); 3.8505 (2.2); 3.8454 (1.2); 3.8355 (2.3); 3.8247 (0.9); 2.9680 (0.8); 2.9588 (0.9); 2.9407 (1.1); 2.9312 (1.1); 2.8005 (1.0); 2.7828 (1.0); 2.7737 (0.9); 2.7636 (0.4); 2.7550 (0.7); 2.6367 (16.0); 2.2866 (13.1); 2.0995 (0.5); 2.0928 (0.6); 2.0826 (1.1); 2.0724 (0.7); 2.0657 (0.7); 2.0552 (0.4); 1.5588 (7.4); 1.2552 (0.5); 1.0432 (0.3); 1.0333 (1.9); 1.0298 (2.1); 1.0275 (1.9); 1.0164 (2.1); 1.0128 (2.2); 1.0035 (0.6); 0.7925 (1.3); 0.7905 (1.2); 0.7869 (1.2); 0.7824 (2.0); 0.7793 (2.1); 0.7771 (2.3); 0.7669 (1.5); 0.7542 (0.3); 0.7485 (0.4); 0.0061 (0.6); −0.0002 (15.6) I-323: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.9094 (5.3); 7.2606 (11.9); 7.2110 (2.8); 7.1079 (0.8); 7.0920 (1.8); 7.0761 (1.2); 7.0049 (0.6); 7.0020 (0.5); 6.9874 (3.2); 6.9775 (4.8); 6.9608 (1.6); 6.8273 (0.8); 6.8138 (1.5); 6.8002 (0.8); 6.1910 (1.7); 4.1962 (0.4); 4.1854 (1.4); 4.1703 (1.5); 4.1593 (0.5); 3.8678 (0.4); 3.8509 (2.3); 3.8356 (2.3); 3.8248 (0.8); 2.9681 (0.9); 2.9589 (0.9); 2.9407 (1.1); 2.9313 (1.1); 2.8006 (1.0); 2.7830 (1.0); 2.7739 (0.8); 2.7639 (0.4); 2.7552 (0.7); 2.6367 (16.0); 2.2866 (13.5); 2.0995 (0.6); 2.0928 (0.7); 2.0827 (1.1); 2.0725 (0.7); 2.0659 (0.7); 2.0554 (0.3); 1.5632 (8.4); 1.3191 (0.4); 1.2557 (0.5); 1.0432 (0.4); 1.0334 (2.0); 1.0298 (2.2); 1.0165 (2.2); 1.0129 (2.2); 1.0036 (0.6); 0.9362 (0.3); 0.9213 (0.6); 0.9062 (0.4); 0.8958 (0.5); 0.7925 (1.4); 0.7869 (1.2); 0.7823 (2.1); 0.7792 (2.2); 0.7773 (2.3); 0.7670 (1.5); −0.0002 (13.2) I-324: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9749 (5.2); 7.6011 (0.4); 7.5834 (1.0); 7.5715 (0.8); 7.5572 (0.5); 7.5530 (0.5); 7.3822 (0.3); 7.3555 (3.7); 7.3377 (2.3); 7.3315 (1.8); 7.3100 (0.3); 7.2987 (3.2); 7.1090 (1.1); 7.0202 (1.9); 6.9943 (2.2); 6.9263 (2.3); 6.8172 (2.0); 6.8128 (2.1); 6.7437 (1.2); 6.6082 (1.2); 6.6025 (1.1); 6.5823 (1.0); 6.5767 (1.0); 6.1224 (1.4); 4.2980 (0.7); 4.2898 (1.0); 4.2639 (1.1); 4.2552 (0.8); 3.9196 (0.4); 3.9079 (0.5); 3.9031 (0.5); 3.8970 (0.5); 3.8932 (0.5); 3.8872 (0.6); 3.8792 (0.6); 3.8674 (1.9); 3.8479 (0.5); 3.8336 (1.4); 3.8132 (0.8); 3.0378 (0.7); 3.0229 (0.7); 2.9929 (1.1); 2.9770 (1.0); 2.7795 (0.9); 2.7477 (0.9); 2.7340 (0.9); 2.7024 (0.8); 2.6734 (16.0); 2.3052 (11.6); 2.0410 (0.6); 1.7615 (0.3); 1.7446 (0.6); 1.7334 (0.6); 1.7166 (1.1); 1.7050 (0.5); 1.6998 (0.7); 1.6886 (0.6); 1.6717 (0.3); 0.9363 (0.4); 0.9202 (1.7); 0.9142 (2.0); 0.9101 (1.5); 0.8922 (1.8); 0.8861 (1.7); 0.8825 (1.3); 0.8708 (0.4); 0.5583 (1.4); 0.5541 (1.0); 0.5486 (1.0); 0.5417 (1.9); 0.5365 (1.7); 0.5322 (1.8); 0.5264 (1.0); 0.5189 (1.0); 0.5162 (1.1); 0.0374 (4.1) I-325: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9534 (5.3); 7.4775 (0.6); 7.4716 (0.6); 7.4511 (1.2); 7.4294 (0.7); 7.4240 (0.7); 7.2988 (2.7); 7.2175 (0.6); 7.2144 (0.6); 7.1906 (1.5); 7.1881 (1.5); 7.1620 (1.1); 7.1362 (0.9); 7.1301 (1.0); 7.1122 (1.0); 7.1072 (1.1); 7.0857 (0.5); 7.0801 (0.5); 7.0163 (1.8); 6.9908 (2.0); 6.9133 (1.0); 6.8900 (2.0); 6.8761 (1.1); 6.8542 (1.1); 6.8168 (1.1); 6.6975 (1.1); 6.6726 (0.9); 6.2088 (1.3); 5.9215 (1.8); 5.9187 (1.9); 5.8624 (1.6); 5.8596 (1.6); 5.4888 (1.8); 5.4861 (1.8); 5.4515 (1.7); 5.4488 (1.7); 4.2993 (0.8); 4.2900 (0.9); 4.2645 (1.0); 4.2552 (1.0); 3.9259 (0.4); 3.9188 (0.4); 3.9142 (0.5); 3.9087 (0.6); 3.9027 (0.5); 3.8979 (0.5); 3.8927 (0.6); 3.8771 (0.5); 3.8687 (0.5); 3.8598 (1.9); 3.8391 (0.7); 3.8250 (1.4); 3.8043 (0.9); 3.0393 (0.7); 3.0236 (0.7); 2.9943 (1.0); 2.9778 (0.9); 2.7861 (1.0); 2.7550 (1.0); 2.7411 (0.8); 2.7093 (0.8); 2.6631 (16.0); 2.3013 (11.2); 2.1600 (10.6); 2.0408 (1.3); 1.6708 (1.2); 0.1094 (0.3); 0.0377 (3.3) I-326: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9465 (5.2); 7.2987 (1.6); 7.1681 (0.4); 7.1480 (1.0); 7.1434 (0.9); 7.1290 (2.8); 7.1223 (1.0); 7.1044 (2.4); 7.0786 (1.0); 7.0559 (0.8); 7.0499 (0.8); 7.0318 (1.1); 7.0212 (2.3); 7.0094 (0.6); 6.9950 (2.2); 6.9030 (2.2); 6.7018 (1.2); 6.6765 (1.0); 6.2424 (1.4); 4.2789 (0.8); 4.2701 (1.0); 4.2448 (1.1); 4.2355 (1.0); 3.9154 (0.4); 3.9039 (0.5); 3.8976 (0.6); 3.8871 (0.6); 3.8833 (0.6); 3.8807 (0.6); 3.8767 (0.5); 3.8668 (0.6); 3.8569 (2.1); 3.8367 (0.6); 3.8225 (1.4); 3.8020 (0.8); 3.0347 (0.7); 3.0189 (0.7); 2.9899 (1.1); 2.9731 (1.0); 2.7940 (1.0); 2.7636 (1.0); 2.7489 (0.8); 2.7181 (0.8); 2.6587 (16.0); 2.3480 (6.9); 2.3409 (7.2); 2.3038 (11.8); 2.1839 (11.0); 2.0366 (2.2); 0.0379 (2.2) I-327: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9563 (5.4); 7.3531 (1.2); 7.3269 (2.6); 7.2986 (10.7); 7.0739 (2.4); 7.0472 (5.4); 7.0162 (1.5); 6.9902 (1.3); 6.8816 (1.0); 6.8787 (1.0); 6.8737 (1.4); 6.8473 (1.5); 6.8444 (1.4); 6.8366 (2.0); 6.8310 (2.4); 6.6090 (1.5); 6.6033 (1.4); 6.5828 (1.3); 6.5770 (1.3); 6.3105 (1.4); 4.2165 (0.9); 4.2056 (1.1); 4.1805 (1.2); 4.1701 (1.6); 4.1472 (0.4); 3.9978 (0.4); 3.9880 (0.6); 3.9677 (0.6); 3.9588 (0.6); 3.9496 (0.5); 3.9419 (0.4); 3.8890 (1.5); 3.8708 (1.0); 3.8530 (1.2); 3.8348 (0.9); 3.1667 (0.9); 3.1504 (0.9); 3.1220 (1.2); 3.1056 (1.1); 2.8944 (1.2); 2.8641 (1.2); 2.8496 (0.9); 2.8192 (0.9); 2.6690 (16.0); 2.0833 (1.9); 1.9740 (0.6); 1.9626 (0.6); 1.9460 (1.2); 1.9291 (0.7); 1.9180 (0.7); 1.9011 (0.4); 1.8061 (0.6); 1.7948 (0.7); 1.7782 (1.2); 1.7615 (0.8); 1.7502 (0.7); 1.7335 (0.4); 1.6431 (0.4); 1.3207 (0.5); 1.2969 (1.1); 1.2730 (0.5); 1.0537 (0.6); 1.0391 (2.0); 1.0321 (2.1); 1.0177 (1.2); 1.0107 (2.1); 1.0038 (2.0); 0.9898 (1.1); 0.9814 (2.3); 0.9746 (2.7); 0.9532 (2.4); 0.9466 (2.4); 0.9280 (0.4); 0.7765 (1.0); 0.7619 (2.4); 0.7453 (2.2); 0.7406 (2.2); 0.7241 (0.8); 0.6161 (1.3); 0.6082 (0.9); 0.5988 (2.0); 0.5915 (2.1); 0.5818 (0.9); 0.5747 (1.4); 0.1069 (7.4); 0.0476 (0.5); 0.0368 (13.8); 0.0276 (0.6); 0.0260 (0.6) I-328: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9519 (5.3); 7.3518 (0.8); 7.3475 (0.5); 7.3233 (1.5); 7.2989 (13.9); 7.1268 (0.4); 7.0119 (1.6); 7.0029 (2.1); 6.9861 (1.5); 6.9769 (2.2); 6.8546 (2.8); 6.8475 (1.9); 6.8233 (4.2); 6.8196 (3.7); 6.5801 (1.1); 6.5743 (1.1); 6.5543 (1.0); 6.5484 (1.0); 6.3248 (1.4); 4.2535 (0.5); 4.2464 (1.1); 4.2214 (1.1); 3.8621 (0.5); 3.8561 (0.6); 3.8471 (0.6); 3.8337 (1.7); 3.8003 (1.5); 3.7799 (0.7); 3.0194 (0.6); 3.0039 (0.6); 2.9739 (1.0); 2.9585 (0.9); 2.7538 (0.8); 2.7232 (0.9); 2.7084 (0.8); 2.6659 (16.0); 2.3399 (0.7); 2.3000 (11.4); 2.0842 (0.5); 1.9752 (0.5); 1.9641 (0.6); 1.9474 (1.1); 1.9304 (0.7); 1.9192 (0.6); 1.9026 (0.3); 1.8072 (0.5); 1.7960 (0.6); 1.7792 (1.0); 1.7621 (0.6); 1.7511 (0.6); 1.6046 (12.9); 1.3448 (0.3); 1.3213 (0.6); 1.3047 (2.2); 1.2984 (2.0); 1.0520 (0.7); 1.0368 (1.9); 1.0300 (2.1); 1.0244 (1.1); 1.0153 (1.1); 1.0084 (2.1); 1.0018 (1.9); 0.9874 (1.0); 0.9605 (0.5); 0.9431 (2.5); 0.9369 (2.8); 0.9200 (3.4); 0.9157 (2.6); 0.9087 (2.2); 0.8968 (1.1); 0.7780 (0.9); 0.7629 (2.2); 0.7566 (2.1); 0.7464 (2.1); 0.7406 (2.4); 0.7246 (0.8); 0.6104 (1.1); 0.6026 (0.9); 0.5972 (1.5); 0.5907 (2.1); 0.5854 (1.4); 0.5736 (1.2); 0.5677 (0.8); 0.1077 (0.9); 0.0491 (0.5); 0.0381 (17.5); 0.0272 (0.7) I-329: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9663 (5.2); 7.3698 (0.8); 7.3429 (2.0); 7.3180 (1.3); 7.3080 (0.5); 7.2989 (12.6); 7.2676 (2.2); 7.0406 (0.7); 7.0342 (0.6); 7.0146 (2.4); 7.0072 (2.1); 6.9945 (1.9); 6.9873 (3.9); 6.9600 (1.2); 6.8367 (0.9); 6.8317 (1.3); 6.8289 (1.3); 6.8057 (3.4); 6.8031 (3.5); 6.3226 (1.3); 4.2259 (0.3); 4.2074 (1.2); 4.1948 (0.6); 4.1822 (1.3); 4.1710 (1.5); 4.1472 (1.4); 4.1234 (0.4); 3.8801 (0.8); 3.8650 (1.8); 3.8501 (0.7); 3.8406 (1.9); 3.8226 (0.6); 3.1222 (0.3); 3.0080 (0.8); 2.9926 (0.7); 2.9584 (1.1); 2.9462 (0.9); 2.8119 (0.9); 2.7833 (0.9); 2.7676 (0.7); 2.7425 (0.8); 2.7375 (0.8); 2.7001 (0.4); 2.6788 (16.0); 2.3392 (0.5); 2.3101 (12.2); 2.2301 (0.4); 2.2062 (0.4); 2.0831 (5.9); 1.9857 (0.6); 1.9746 (0.6); 1.9577 (1.2); 1.9408 (0.8); 1.9299 (0.7); 1.9127 (0.4); 1.7536 (0.6); 1.3208 (1.7); 1.2969 (3.5); 1.2732 (1.7); 1.0633 (0.7); 1.0480 (1.9); 1.0412 (2.2); 1.0263 (1.2); 1.0196 (2.1); 1.0131 (1.9); 0.9984 (1.1); 0.7800 (0.9); 0.7646 (2.4); 0.7588 (2.2); 0.7484 (2.1); 0.7425 (2.6); 0.7262 (0.9); 0.1069 (1.2); 0.0479 (0.5); 0.0371 (16.6); 0.0262 (0.7) I-330: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9422 (5.1); 7.3307 (1.1); 7.2985 (8.6); 7.2785 (1.4); 6.9987 (1.5); 6.9675 (3.0); 6.9127 (6.3); 6.9097 (6.0); 6.8317 (1.0); 6.8286 (1.0); 6.8237 (1.4); 6.8209 (1.1); 6.8052 (0.6); 6.7974 (1.6); 6.7939 (1.7); 6.7898 (2.0); 6.7841 (2.3); 6.7780 (1.0); 6.3312 (1.4); 5.3371 (3.1); 4.2797 (0.9); 4.2684 (1.0); 4.2440 (1.0); 4.2326 (1.1); 3.8992 (0.4); 3.8827 (0.6); 3.8671 (0.6); 3.8509 (0.4); 3.8013 (1.7); 3.7795 (1.0); 3.7657 (1.4); 3.7439 (1.0); 2.9825 (0.8); 2.9663 (0.8); 2.9378 (1.0); 2.9213 (1.0); 2.6824 (1.2); 2.6593 (16.0); 2.6377 (1.0); 2.6062 (0.9); 2.1764 (11.8); 2.1164 (11.9); 1.9592 (0.6); 1.9479 (0.6); 1.9313 (1.1); 1.9144 (0.7); 1.9032 (0.8); 1.8864 (0.3); 1.6225 (3.6); 1.2972 (0.4); 1.0497 (0.7); 1.0351 (1.9); 1.0280 (2.1); 1.0219 (1.0); 1.0135 (1.0); 1.0066 (2.0); 1.0000 (1.9); 0.9856 (0.9); 0.7610 (0.9); 0.7463 (2.4); 0.7415 (2.0); 0.7295 (2.0); 0.7246 (2.3); 0.7081 (0.7); 0.0483 (0.4); 0.0375 (11.6); 0.0284 (0.4); 0.0267 (0.4) I-331: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9512 (4.1); 7.5078 (1.7); 7.3604 (1.2); 7.3341 (1.4); 7.2987 (13.0); 7.1394 (0.4); 7.1354 (0.4); 7.1126 (1.2); 7.0869 (1.5); 7.0674 (0.9); 7.0552 (0.8); 7.0489 (0.9); 7.0313 (0.8); 7.0260 (0.9); 7.0045 (0.4); 6.9988 (0.4); 6.8570 (0.6); 6.8508 (0.6); 6.8301 (0.9); 6.8088 (0.5); 6.8030 (0.4); 6.6654 (0.8); 6.4780 (1.7); 6.2907 (0.8); 6.2041 (0.8); 4.2067 (0.7); 4.1964 (0.9); 4.1709 (1.1); 4.1606 (1.1); 4.0772 (0.5); 4.0619 (0.5); 4.0478 (0.5); 4.0020 (1.2); 3.9870 (0.7); 3.9661 (0.8); 3.9510 (0.6); 3.2872 (0.5); 3.2710 (0.5); 3.2431 (0.7); 3.2263 (0.7); 3.0858 (0.8); 3.0556 (0.8); 3.0415 (0.6); 3.0112 (0.5); 2.6810 (12.4); 2.5382 (0.4); 2.1233 (0.4); 2.1119 (0.4); 2.0951 (0.7); 2.0833 (0.8); 2.0778 (0.5); 2.0667 (0.4); 1.6021 (16.0); 1.2968 (0.5); 1.0876 (0.4); 1.0734 (1.2); 1.0667 (1.4); 1.0561 (0.8); 1.0522 (0.7); 1.0448 (1.3); 1.0385 (1.3); 1.0270 (0.5); 1.0242 (0.5); 0.8201 (0.7); 0.8131 (0.7); 0.8044 (1.4); 0.7971 (1.4); 0.7881 (1.6); 0.7810 (1.0); 0.7708 (0.6); 0.1065 (4.3); 0.0474 (0.6); 0.0367 (17.1); 0.0258 (0.7) I-332: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9550 (5.2); 7.2987 (12.4); 7.2597 (2.3); 7.2318 (2.6); 7.1624 (2.2); 7.1543 (2.2); 7.1213 (1.5); 7.0930 (1.5); 7.0773 (1.1); 7.0706 (1.3); 7.0539 (1.1); 7.0483 (1.3); 7.0271 (0.6); 7.0212 (0.5); 6.8631 (0.7); 6.8564 (0.7); 6.8390 (1.1); 6.8150 (0.7); 6.8091 (0.6); 6.7384 (1.2); 6.7303 (1.1); 6.7107 (1.0); 6.7025 (1.0); 6.5663 (1.6); 6.3222 (3.1); 6.2061 (1.1); 6.0783 (1.6); 4.2068 (0.8); 4.1966 (1.1); 4.1710 (1.8); 4.1615 (1.3); 4.1470 (0.6); 4.0496 (0.4); 4.0389 (0.6); 4.0234 (0.6); 4.0090 (0.6); 3.9997 (0.4); 3.9931 (0.5); 3.9797 (1.6); 3.9643 (0.8); 3.9443 (1.1); 3.9286 (0.8); 3.2239 (0.8); 3.2082 (0.8); 3.1793 (1.2); 3.1630 (1.1); 3.0126 (1.2); 2.9828 (1.1); 2.9679 (0.8); 2.9375 (0.8); 2.6802 (16.0); 2.5653 (0.6); 2.1299 (0.4); 2.1187 (0.5); 2.1016 (1.0); 2.0831 (3.1); 2.0736 (0.6); 1.6050 (6.4); 1.3437 (0.7); 1.3205 (1.7); 1.3032 (3.8); 1.2968 (4.5); 1.2729 (1.0); 1.0908 (0.5); 1.0769 (1.6); 1.0699 (1.8); 1.0568 (0.9); 1.0482 (1.8); 1.0417 (1.7); 1.0283 (0.8); 0.9405 (1.3); 0.9187 (4.4); 0.8955 (1.6); 0.8256 (0.9); 0.8085 (1.9); 0.8038 (1.6); 0.7946 (1.9); 0.7918 (1.9); 0.7866 (1.4); 0.7748 (0.8); 0.1066 (4.5); 0.0474 (0.6); 0.0367 (17.6); 0.0257 (0.7) I-333: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9621 (5.3); 7.5684 (0.6); 7.5423 (1.6); 7.5160 (1.2); 7.4585 (1.5); 7.4329 (0.9); 7.2991 (1.3); 7.2627 (1.9); 7.2293 (1.0); 7.2260 (1.2); 7.2223 (1.1); 7.2187 (0.8); 7.2027 (0.9); 7.1993 (1.0); 7.1954 (0.9); 7.1919 (0.7); 7.1344 (2.2); 7.1320 (2.3); 7.0793 (2.1); 7.0537 (2.4); 6.8868 (1.1); 6.7649 (1.3); 6.7618 (1.3); 6.7393 (1.1); 6.7362 (1.1); 6.6990 (2.3); 6.5112 (1.2); 6.1963 (1.3); 5.3271 (5.4); 4.2354 (0.9); 4.2245 (1.0); 4.1993 (1.1); 4.1885 (1.2); 4.0357 (0.4); 4.0264 (0.5); 4.0185 (0.5); 4.0112 (0.6); 4.0048 (0.6); 3.9963 (0.6); 3.9874 (0.5); 3.9795 (0.4); 3.8981 (1.5); 3.8797 (1.1); 3.8620 (1.2); 3.8436 (1.0); 3.1666 (0.8); 3.1503 (0.8); 3.1217 (1.1); 3.1055 (1.0); 2.9205 (1.2); 2.8894 (1.1); 2.8758 (1.0); 2.8445 (0.8); 2.6641 (16.0); 2.2075 (11.0); 1.7663 (0.9); 0.0325 (1.4) I-334: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9519 (5.2); 7.2988 (13.0); 7.2702 (2.7); 7.2584 (1.7); 7.2530 (1.7); 7.1430 (0.5); 7.1397 (0.5); 7.1160 (1.5); 7.0879 (1.5); 7.0735 (1.0); 7.0667 (1.2); 7.0500 (1.1); 7.0445 (1.2); 7.0232 (0.6); 7.0173 (0.5); 6.8570 (0.8); 6.8501 (1.4); 6.8415 (1.1); 6.8344 (1.5); 6.8218 (1.0); 6.8183 (1.0); 6.8101 (1.2); 6.2116 (1.1); 5.3376 (3.4); 4.1907 (0.7); 4.1814 (1.1); 4.1557 (1.3); 4.1464 (1.2); 4.0549 (0.4); 4.0439 (0.6); 4.0287 (0.7); 4.0151 (0.7); 3.9978 (1.8); 3.9833 (0.6); 3.9625 (1.0); 3.9479 (0.7); 3.2400 (0.7); 3.2245 (0.7); 3.1956 (1.2); 3.1792 (1.1); 3.0479 (1.0); 3.0184 (1.0); 3.0030 (0.8); 2.9734 (0.7); 2.6824 (16.0); 2.1260 (0.5); 2.1147 (0.5); 2.0975 (0.9); 2.0808 (0.6); 2.0694 (0.5); 1.6072 (9.5); 1.0835 (0.5); 1.0709 (1.6); 1.0641 (1.8); 1.0517 (0.9); 1.0423 (1.7); 1.0358 (1.7); 1.0231 (0.7); 0.8184 (1.0); 0.8013 (2.0); 0.7965 (1.6); 0.7874 (1.8); 0.7846 (1.8); 0.7795 (1.4); 0.7675 (0.7); 0.1066 (3.8); 0.0474 (0.6); 0.0366 (15.6); 0.0257 (0.6) I-335: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9551 (4.9); 7.2986 (14.6); 7.1298 (0.5); 7.1263 (0.5); 7.1030 (1.4); 7.1001 (1.3); 7.0767 (1.0); 7.0736 (1.0); 7.0329 (1.9); 7.0218 (0.9); 7.0159 (1.1); 7.0076 (2.2); 6.9929 (1.2); 6.9711 (0.6); 6.9657 (0.5); 6.8537 (0.7); 6.8484 (0.7); 6.8270 (1.2); 6.8056 (0.6); 6.8007 (0.5); 6.7277 (2.1); 6.6924 (1.2); 6.6675 (1.0); 6.2726 (1.3); 5.3378 (12.4); 4.3082 (0.8); 4.2966 (0.9); 4.2722 (0.9); 4.2608 (1.0); 4.1713 (0.4); 4.1475 (0.4); 4.0277 (0.5); 4.0146 (0.6); 4.0078 (0.5); 3.9959 (0.4); 3.8839 (1.4); 3.8631 (1.0); 3.8478 (1.1); 3.8270 (0.9); 3.2672 (0.7); 3.2499 (0.7); 3.2221 (0.9); 3.2047 (0.9); 2.9493 (1.0); 2.9177 (1.0); 2.9038 (0.8); 2.8726 (0.7); 2.6668 (14.7); 2.1789 (10.4); 2.1388 (0.4); 2.1283 (0.5); 2.1109 (1.0); 2.0935 (0.6); 2.0837 (2.3); 2.0461 (0.5); 1.9572 (0.5); 1.9468 (0.5); 1.9408 (0.3); 1.9292 (0.9); 1.9115 (0.5); 1.9011 (0.5); 1.6037 (16.0); 1.3210 (0.7); 1.2971 (1.4); 1.2734 (0.6); 1.0862 (0.6); 1.0731 (1.4); 1.0660 (1.7); 1.0614 (1.0); 1.0582 (1.0); 1.0530 (1.0); 1.0442 (1.4); 1.0378 (1.6); 1.0246 (0.8); 1.0046 (0.3); 0.9894 (0.5); 0.9750 (1.2); 0.9604 (1.4); 0.9545 (1.1); 0.9461 (1.3); 0.9323 (1.2); 0.9167 (0.7); 0.9014 (0.4); 0.8301 (0.8); 0.8133 (1.7); 0.8077 (1.5); 0.7985 (1.8); 0.7911 (1.2); 0.7802 (0.6); 0.6935 (0.6); 0.6826 (1.2); 0.6648 (2.1); 0.6550 (1.0); 0.6471 (1.0); 0.6378 (0.6); 0.1067 (4.2); 0.0478 (0.7); 0.0462 (0.5); 0.0370 (19.2); 0.0294 (0.6); 0.0278 (0.6); 0.0262 (0.7) I-336: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.9211 (5.3); 7.3693 (1.0); 7.3561 (2.0); 7.3537 (1.9); 7.3403 (1.7); 7.2620 (6.0); 7.2120 (3.5); 7.1871 (1.3); 7.1844 (1.4); 7.1678 (2.4); 7.1515 (1.8); 7.1066 (1.3); 7.0931 (2.1); 7.0773 (1.4); 7.0433 (1.5); 7.0271 (2.6); 6.9794 (3.1); 6.9632 (2.5); 6.0258 (2.4); 5.2989 (0.4); 4.1931 (1.7); 4.1775 (2.0); 3.8593 (3.1); 3.8428 (2.9); 3.8322 (1.9); 3.4869 (7.2); 2.9726 (0.9); 2.9632 (1.2); 2.9552 (1.4); 2.9456 (1.8); 2.9357 (1.9); 2.8816 (0.8); 2.8029 (1.0); 2.7931 (0.7); 2.7842 (1.4); 2.7756 (1.4); 2.7570 (1.2); 2.6442 (16.0); 2.2905 (14.1); 1.5839 (5.6); −0.0002 (7.4) I-337: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.0116 (0.5); 7.9208 (5.2); 7.3719 (0.7); 7.3689 (0.8); 7.3558 (1.6); 7.3527 (1.1); 7.3425 (0.9); 7.3396 (1.0); 7.2619 (6.3); 7.2121 (2.6); 7.1867 (0.8); 7.1837 (0.8); 7.1702 (1.6); 7.1672 (1.8); 7.1538 (1.0); 7.1509 (1.1); 7.1095 (1.0); 7.1065 (1.1); 7.0960 (1.1); 7.0932 (1.6); 7.0797 (0.7); 7.0767 (0.7); 7.0467 (1.0); 7.0433 (1.0); 7.0305 (1.6); 7.0271 (1.7); 6.9794 (2.9); 6.9632 (1.8); 6.0277 (1.6); 4.1927 (1.3); 4.1772 (1.4); 3.8840 (0.4); 3.8785 (0.6); 3.8733 (0.7); 3.8620 (2.1); 3.8426 (1.7); 3.8318 (0.9); 3.4866 (1.9); 2.9726 (0.8); 2.9630 (0.9); 2.9547 (3.7); 2.9455 (1.4); 2.9355 (1.2); 2.8812 (3.2); 2.8031 (1.0); 2.7934 (0.4); 2.7845 (1.0); 2.7758 (0.9); 2.7571 (0.8); 2.6439 (16.0); 2.2905 (12.9); 1.5854 (6.9); −0.0002 (8.0) I-338: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.9181 (5.2); 7.3573 (0.7); 7.3502 (0.8); 7.3446 (1.3); 7.3377 (1.4); 7.3315 (0.8); 7.3248 (0.8); 7.2614 (5.6); 7.1672 (0.5); 7.1620 (0.6); 7.1523 (3.8); 7.1450 (2.5); 7.1381 (3.2); 7.1280 (0.4); 7.1234 (0.4); 7.1092 (2.6); 7.0620 (2.2); 7.0466 (2.4); 6.7473 (1.4); 6.7329 (1.2); 5.9996 (1.4); 4.2072 (1.1); 4.2005 (1.2); 4.1853 (1.2); 4.1787 (1.2); 4.0190 (0.6); 4.0129 (0.7); 4.0077 (0.7); 4.0041 (0.7); 4.0009 (0.7); 3.9955 (0.7); 3.9896 (0.5); 3.9852 (0.4); 3.8755 (1.5); 3.8645 (1.3); 3.8536 (1.3); 3.8427 (1.1); 3.4865 (0.3); 3.1426 (1.0); 3.1325 (1.0); 3.1157 (1.2); 3.1056 (1.0); 2.8876 (1.2); 2.8689 (1.2); 2.8607 (1.0); 2.8420 (0.9); 2.6413 (16.0); 2.1865 (11.8); 1.5792 (4.8); 0.0061 (0.6); −0.0002 (7.2) I-339: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.9180 (5.2); 7.3574 (0.6); 7.3503 (0.7); 7.3447 (1.3); 7.3379 (1.4); 7.3316 (0.8); 7.3250 (0.9); 7.2616 (5.6); 7.1523 (3.6); 7.1451 (2.5); 7.1383 (3.4); 7.1284 (0.5); 7.1238 (0.4); 7.1091 (3.0); 7.0620 (2.3); 7.0466 (2.6); 6.7475 (1.6); 6.7323 (1.5); 5.9992 (1.6); 4.2071 (1.1); 4.2005 (1.2); 4.1853 (1.3); 4.1786 (1.4); 4.0189 (0.5); 4.0127 (0.7); 4.0073 (0.8); 4.0009 (0.8); 3.9956 (0.8); 3.9897 (0.6); 3.8756 (1.4); 3.8647 (1.3); 3.8537 (1.3); 3.8428 (1.2); 3.1426 (1.0); 3.1325 (1.0); 3.1157 (1.2); 3.1056 (1.2); 2.9550 (1.8); 2.8876 (1.3); 2.8824 (1.9); 2.8691 (1.3); 2.8609 (1.1); 2.8422 (1.0); 2.6414 (16.0); 2.1865 (12.7); 1.5834 (4.2); −0.0002 (6.8) I-340: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.6087 (16.0); 7.5194 (4.3); 7.5035 (7.6); 7.4877 (4.6); 7.4666 (1.1); 7.4573 (7.9); 7.4532 (8.0); 7.4417 (0.7); 7.4294 (5.7); 7.4130 (6.6); 7.3656 (0.4); 7.2775 (5.8); 7.2734 (5.8); 7.2603 (48.1); 6.9052 (7.5); 6.8898 (7.0); 6.6143 (5.3); 6.5980 (5.0); 5.2992 (14.3); 4.4164 (1.7); 4.4019 (2.9); 4.3870 (1.6); 4.3079 (4.0); 4.3056 (4.1); 4.2859 (4.4); 4.2837 (4.4); 3.9983 (3.5); 3.9944 (3.6); 3.9765 (3.1); 3.9725 (2.9); 3.3313 (2.2); 3.3177 (2.2); 3.3036 (3.0); 3.2900 (2.8); 3.1815 (3.5); 3.1654 (3.4); 3.1537 (2.5); 3.1376 (2.3); 1.7006 (0.4); 1.5621 (3.7); 1.4796 (0.5); 1.2544 (1.7); 0.1164 (0.4); 0.0691 (2.5); 0.0059 (3.3); − 0.0002 (48.0); −0.0064 (2.3) I-341: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1297 (16.0); 7.4699 (2.1); 7.4440 (6.0); 7.4181 (5.1); 7.3933 (5.2); 7.3673 (2.2); 7.3413 (6.7); 7.3343 (6.9); 7.2988 (6.5); 7.1470 (5.9); 7.1404 (4.2); 7.1338 (5.4); 7.1276 (4.2); 7.1198 (7.4); 6.9887 (2.4); 6.9844 (2.7); 6.9811 (2.6); 6.9770 (2.2); 6.9629 (2.2); 6.9585 (2.4); 6.9550 (2.4); 6.9508 (2.1); 6.9423 (4.5); 6.9352 (4.3); 6.9151 (3.4); 6.9080 (3.3); 6.7956 (2.5); 6.7594 (2.8); 6.7371 (3.0); 6.7009 (3.0); 6.2353 (2.9); 6.2284 (2.9); 5.8228 (6.0); 5.7644 (5.3); 5.3864 (5.8); 5.3500 (5.5); 4.1904 (2.3); 4.1802 (2.7); 4.1545 (3.1); 4.1443 (3.4); 4.0496 (0.4); 4.0389 (0.7); 4.0330 (1.0); 4.0225 (1.6); 4.0162 (1.2); 4.0059 (1.6); 3.9934 (1.7); 3.9835 (1.1); 3.9763 (1.1); 3.9665 (0.6); 3.9464 (4.0); 3.9304 (2.4); 3.9105 (2.8); 3.8945 (2.1); 3.1832 (2.0); 3.1661 (2.0); 3.1382 (3.2); 3.1210 (3.0); 2.9885 (3.2); 2.9586 (3.0); 2.9436 (2.2); 2.9134 (2.0); 2.0373 (3.0); 0.0366 (7.8) I-342: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.6222 (1.3); 7.6026 (7.2); 7.5822 (4.1); 7.5102 (1.9); 7.4729 (0.7); 7.4633 (1.1); 7.4558 (0.8); 7.4423 (0.7); 7.4353 (0.4); 7.2989 (14.4); 7.0479 (1.4); 7.0219 (3.9); 6.9452 (1.2); 6.9185 (0.7); 4.9396 (1.1); 4.9305 (1.2); 3.9820 (0.7); 3.9725 (0.9); 3.9475 (1.1); 3.9375 (1.1); 3.8707 (16.0); 3.8532 (1.1); 3.8329 (1.2); 3.8177 (0.5); 3.8102 (0.6); 3.7996 (0.6); 3.7913 (0.5); 3.7734 (1.6); 3.7575 (0.6); 3.7384 (0.9); 3.7221 (0.6); 2.9365 (0.4); 2.9182 (0.4); 2.8911 (1.1); 2.8720 (1.0); 2.8510 (1.0); 2.8228 (1.0); 2.8059 (0.4); 2.7768 (0.4); 2.3184 (10.4); 2.3083 (10.4); 1.6113 (7.9); 1.2982 (0.8); 1.2923 (0.9); 0.1073 (2.2); 0.0481 (0.6); 0.0375 (15.7); 0.0266 (0.6) I-343: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.5808 (1.1); 7.5613 (2.9); 7.5583 (2.6); 7.4230 (1.4); 7.3975 (0.6); 7.3872 (0.8); 7.3798 (0.6); 7.3667 (0.6); 7.3594 (0.4); 7.2990 (3.6); 7.0397 (1.2); 7.0264 (1.7); 7.0148 (1.9); 6.9393 (1.0); 6.9137 (0.6); 4.8214 (1.0); 4.2075 (0.8); 4.1817 (0.9); 3.9625 (0.4); 3.9422 (1.4); 3.9260 (0.4); 3.9142 (1.1); 3.8970 (0.4); 3.0469 (0.4); 3.0300 (0.4); 3.0006 (0.7); 2.9834 (0.6); 2.9027 (0.6); 2.8746 (0.6); 2.8571 (0.4); 2.8279 (0.3); 2.3142 (16.0); 2.0709 (0.4); 2.0617 (0.4); 2.0421 (0.9); 2.0223 (0.5); 2.0132 (0.5); 1.6259 (0.8); 1.2927 (0.4); 1.2821 (0.4); 1.2642 (1.4); 1.2602 (1.4); 1.2529 (1.0); 1.2443 (0.7); 1.2354 (1.0); 1.2313 (1.2); 1.2244 (0.8); 1.2155 (0.4); 1.0466 (0.8); 1.0392 (0.7); 1.0361 (0.8); 1.0317 (0.9); 1.0260 (1.2); 1.0201 (1.2); 1.0057 (0.6); 1.0017 (0.7); 0.1088 (0.5); 0.0379 (3.9) I-344: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9635 (5.2); 7.5882 (0.5); 7.5627 (0.8); 7.5496 (0.5); 7.5399 (0.5); 7.4082 (0.3); 7.3875 (1.0); 7.3856 (1.0); 7.3814 (0.8); 7.3656 (3.1); 7.3588 (0.9); 7.3421 (1.4); 7.3142 (0.4); 7.2986 (2.2); 7.1401 (2.1); 7.1377 (2.1); 7.1032 (2.1); 7.0935 (1.2); 7.0776 (2.4); 6.9109 (2.2); 6.7749 (1.2); 6.7720 (1.2); 6.7493 (1.0); 6.7463 (1.0); 6.7283 (1.1); 6.0664 (1.2); 4.2522 (0.9); 4.2414 (1.0); 4.2161 (1.1); 4.2052 (1.2); 4.0622 (0.4); 4.0524 (0.5); 4.0435 (0.5); 4.0369 (0.5); 4.0315 (0.6); 4.0227 (0.6); 4.0131 (0.4); 3.9230 (1.4); 3.9049 (1.1); 3.8868 (1.2); 3.8687 (0.9); 3.1924 (0.8); 3.1758 (0.8); 3.1476 (1.1); 3.1310 (1.0); 2.9369 (1.1); 2.9060 (1.1); 2.8921 (0.9); 2.8612 (0.8); 2.6743 (16.0); 2.2035 (0.5); 2.1894 (10.8); 2.0383 (0.4); 0.0341 (2.9) I-345: ¹H-NMR(300.2 MHz, CDCl3): δ = 10.3610 (4.4); 9.9815 (0.4); 7.9845 (5.2); 7.8765 (0.7); 7.8705 (0.7); 7.8565 (0.7); 7.8504 (1.4); 7.8446 (0.8); 7.8308 (0.8); 7.8247 (0.7); 7.7702 (0.4); 7.5012 (0.6); 7.4953 (0.6); 7.4746 (1.2); 7.4695 (1.1); 7.4504 (1.0); 7.4442 (0.9); 7.3962 (1.2); 7.3699 (1.6); 7.3435 (0.6); 7.2987 (4.6); 7.0310 (1.8); 7.0056 (2.1); 6.8927 (2.0); 6.7094 (1.1); 6.6850 (1.0); 6.0840 (1.3); 4.3229 (0.8); 4.3127 (1.0); 4.2875 (1.0); 4.2775 (1.1); 3.9565 (0.4); 3.9487 (0.4); 3.9388 (0.5); 3.9328 (0.5); 3.9276 (0.5); 3.9227 (0.6); 3.9172 (0.5); 3.9069 (0.5); 3.8988 (0.4); 3.8913 (0.4); 3.8827 (1.8); 3.8622 (0.8); 3.8476 (1.4); 3.8270 (0.9); 3.0569 (0.7); 3.0407 (0.7); 3.0117 (1.0); 2.9951 (1.0); 2.8022 (1.1); 2.7706 (1.0); 2.7570 (0.8); 2.7331 (1.2); 2.7250 (0.8); 2.6806 (16.0); 2.3094 (11.6); 2.2605 (0.9); 2.1483 (10.8); 2.0439 (3.1); 0.0355 (6.4) I-346: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9573 (5.1); 7.3432 (1.2); 7.3170 (2.6); 7.2988 (8.8); 7.2908 (1.7); 7.1491 (2.1); 7.0760 (2.0); 7.0504 (2.3); 7.0118 (1.4); 6.9859 (1.2); 6.8761 (0.9); 6.8731 (1.0); 6.8682 (1.2); 6.8652 (1.1); 6.8493 (0.8); 6.8462 (0.8); 6.8414 (1.1); 6.8383 (1.0); 6.8018 (1.6); 6.7956 (2.1); 6.7887 (1.2); 6.7342 (1.2); 6.7310 (1.2); 6.7086 (1.0); 6.7054 (1.0); 6.3037 (1.1); 4.2237 (0.9); 4.2129 (1.0); 4.1877 (1.1); 4.1768 (1.2); 4.0210 (0.4); 4.0104 (0.5); 4.0025 (0.5); 3.9908 (0.6); 3.9820 (0.6); 3.9728 (0.4); 3.8919 (1.4); 3.8735 (1.0); 3.8559 (1.2); 3.8375 (0.9); 3.1723 (0.8); 3.1556 (0.8); 3.1275 (1.0); 3.1108 (1.0); 2.9090 (1.1); 2.8787 (1.1); 2.8643 (0.8); 2.8338 (0.8); 2.6689 (16.0); 2.2369 (10.5); 2.0835 (0.8); 1.9668 (0.5); 1.9557 (0.6); 1.9389 (1.1); 1.9222 (0.6); 1.9110 (0.6); 1.6146 (3.4); 1.3208 (0.6); 1.3035 (1.6); 1.2972 (1.7); 1.2733 (0.3); 1.0554 (0.6); 1.0409 (1.7); 1.0340 (2.0); 1.0277 (0.9); 1.0195 (0.9); 1.0123 (1.9); 1.0059 (1.7); 0.9918 (0.8); 0.9406 (0.7); 0.9191 (1.8); 0.8959 (0.7); 0.7671 (1.0); 0.7528 (2.0); 0.7499 (1.9); 0.7454 (1.8); 0.7395 (1.2); 0.7361 (2.0); 0.7317 (1.9); 0.7287 (1.7); 0.7150 (0.8); 0.1071 (0.4); 0.0480 (0.4); 0.0371 (12.1); 0.0262 (0.5) I-347: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.1955 (0.3); 8.1353 (11.6); 8.1319 (12.5); 8.0891 (1.0); 8.0855 (1.0); 7.8055 (0.4); 7.7711 (0.4); 7.7591 (0.4); 7.7464 (0.5); 7.7271 (0.5); 7.6582 (0.7); 7.5742 (16.0); 7.5017 (10.4); 7.4703 (1.4); 7.4205 (6.6); 7.4089 (5.7); 7.3503 (6.6); 7.3378 (26.2); 7.3229 (14.5); 7.3092 (7.6); 7.2961 (6.7); 7.2925 (6.5); 7.2822 (6.0); 7.2633 (19.1); 7.2596 (19.8); 7.2296 (1.6); 7.1952 (1.0); 7.1842 (1.0); 7.1408 (1.3); 7.1257 (1.1); 7.0886 (0.4); 7.0481 (0.4); 7.0293 (0.4); 7.0052 (0.3); 6.9853 (0.3); 6.9670 (0.4); 6.9329 (0.3); 6.8675 (0.3); 6.8335 (0.3); 6.7718 (0.3); 6.7173 (6.0); 6.6855 (6.6); 6.1720 (3.7); 6.1568 (4.0); 6.1404 (3.6); 6.1252 (3.7); 6.0942 (7.3); 5.9845 (0.5); 4.3792 (4.4); 4.2813 (3.9); 4.2612 (4.4); 4.0964 (0.4); 4.0725 (0.4); 3.8190 (3.9); 3.8058 (4.1); 3.8002 (4.0); 3.7971 (4.0); 3.7844 (3.5); 3.6330 (0.3); 2.7611 (0.4); 2.7453 (0.4); 2.1688 (0.3); 1.9937 (0.3); 1.9805 (0.6); 1.9665 (0.6); 1.9496 (0.3); 1.5768 (2.4); 1.3662 (0.4); 1.3325 (0.4); 1.2552 (1.2); 0.0701 (2.3); 0.0036 (19.3); −0.0002 (21.7) I-348: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9593 (5.2); 7.4751 (0.7); 7.4681 (0.8); 7.4547 (0.8); 7.4506 (0.9); 7.4439 (1.4); 7.4337 (0.8); 7.4233 (0.8); 7.2987 (8.1); 7.2526 (0.4); 7.2456 (0.5); 7.2251 (1.4); 7.2183 (1.2); 7.2060 (4.1); 7.1965 (1.3); 7.1835 (1.8); 7.1546 (0.6); 7.0155 (1.8); 6.9901 (2.1); 6.9038 (2.0); 6.7288 (1.1); 6.7030 (0.9); 6.1207 (1.3); 4.3083 (0.8); 4.2987 (0.9); 4.2728 (1.0); 4.2636 (1.0); 3.9301 (0.4); 3.9229 (0.4); 3.9178 (0.5); 3.9125 (0.6); 3.9068 (0.5); 3.9021 (0.5); 3.8967 (0.6); 3.8809 (0.5); 3.8723 (0.5); 3.8612 (1.8); 3.8405 (0.7); 3.8263 (1.4); 3.8056 (0.9); 3.3798 (4.0); 3.0440 (0.7); 3.0283 (0.7); 2.9991 (1.0); 2.9827 (1.0); 2.7831 (1.1); 2.7517 (1.0); 2.7378 (0.9); 2.7315 (0.7); 2.7062 (0.8); 2.6689 (16.0); 2.3057 (11.4); 2.2881 (1.1); 2.1877 (10.7); 2.1559 (0.5); 2.0452 (2.4); 0.0480 (0.4); 0.0372 (11.0); 0.0264 (0.5)

The compounds as shown in table 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 25, 27, 29, 31, 33, 35, 37, 39, 41 and 43 below were prepared in analogy with the examples provided above or following methods described herein. ¹H-NMR data of these compounds is respectively shown in tables 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 30, 32, 34, 36, 38 40, 42 and 44.

TABLE 3 Compounds according to formula (1)

Ex N^(o) R⁷ R⁸ Q U¹ LogP 1-01 Cl H 3-(difluoromethyl)phenyl hydroxy 1.45^([a]) 1-02 Cl methyl 3-cyclopropyl-2-fluorophenyl hydroxy 1.84^([a]) 1-03 methyl H 3-(trifluoromethyl)phenyl methoxy(methyl)amino 2.33^([a]) 1-04 Cl methyl 3-(trifluoromethyl)phenyl hydroxy 1.70^([a]) 1-05 Cl cyclopropylamino 3-(trifluoromethyl)phenyl hydroxy 2.20^([a]) 1-06 Cl H 3-cyclopropylphenyl hydroxy 1.87^([a]) 1-07 Cl H 3-(trifluoromethyl)phenyl methoxy(methyl)amino 2.90^([a]) 1-08 Cl H 3-(difluoromethyl)-2-fluorophenyl isopropyloxy 3.68^([a]) 1-09 Cl cyclopropylamino 3-(trifluoromethyl)phenyl methoxy 3.35^([a]) 1-10 Cl H 3-cyclopropyl-2-fluorophenyl hydroxy 2.01^([a]) 1-11 ethyl H 3-(trifluoromethyl)phenyl hydroxy 1.82^([a]) 1-12 ethyl H 3-(trifluoromethyl)phenyl isopropyloxy 3.96^([a]) 1-13 acetyl H 3-(trifluoromethyl)phenyl hydroxy 2.01^([a]) 1-14 methyl H 3-(trifluoromethyl)phenyl methoxy 2.77^([a]) 1-15 vinyl H 3-(trifluoromethyl)phenyl isopropyloxy 4.01^([a]) 1-16 methyl H 3-cyclopropylphenyl hydroxy 1.46^([a]) 1-17 methyl H 2-fluoro-3-(trifluoromethyl)phenyl methoxy 2.90^([a]) 1-18 Cl H 2-fluoro-3-(trifluoromethyl)phenyl hydroxy 1.98^([a]) 1-19 Cl H 2-fluoro-3-(trifluoromethyl)phenyl methoxy 3.35^([a]) 1-20 Cl I 3-(trifluoromethyl)phenyl methoxy 3.25^([a]) 1-21 Cl H 3-cyclopropyl-2-fluorophenyl isopropyloxy 4.30^([a]) 1-22 Cl H 3-cyclopropylphenyl isopropyloxy 4.15^([a]) 1-23 Cl H 3-(difluoromethyl)-2-fluorophenyl hydroxy 1.63^([a]) 1-24 Cl methyl 3-cyclopropyl-2-fluorophenyl isopropyloxy 4.51^([a]) 1-25 I H 3-(trifluoromethyl)phenyl isopropyloxy 4.25^([a]) 1-26 methyl H 2-fluoro-3-(trifluoromethyl)phenyl hydroxy 1.75^([a]) 1-27 methyl methyl 3-(trifluoromethyl)phenyl hydroxy 1.52^([a]) 1-28 1-ethoxyethen-1-yl H 3-(trifluoromethyl)phenyl isopropyloxy 4.90^([a]) 1-29 acetyl H 3-(trifluoromethyl)phenyl isopropyloxy 3.99^([a]) 1-30 methyl H 3-cyclopropyl-2-fluorophenyl hydroxy 1.70^([a]) 1-31 methyl methyl 3-(trifluoromethyl)phenyl methoxy 2.98^([a]) 1-32 Cl H 3-(trifluoromethyl)phenyl isopropyloxy 4.06^([a]) 1-33 Cl methyl 3-(trifluoromethyl)phenyl methoxy 3.55^([a]) 1-34 Cl H 6-chloro-5-(trifluoromethyl)pyridin-3-yl hydroxy 1.14^([a]) 1-35 Cl H 6-chloro-5-(trifluoromethyl)pyridin-3-yl ethoxy 3.74^([a]) 1-36 Cl H 5-bromopyridin-3-yl hydroxy 0.94^([a]); 0.53^([a]) 1-37 Cl H 3-(1-fluorocyclopropyl)phenyl hydroxy 1.82^([a]) 1-38 Cl H 3-(1-fluorocyclopropyl)phenyl isopropyloxy 3.99^([a]) 1-39 Cl H 2-fluoro-3-[rac-2,2-difluorocyclopropyl]phenyl hydroxy 1.95^([a]) 1-40 Cl H 2-fluoro-3-[rac-2,2-difluorocyclopropyl]phenyl isopropyloxy 3.96^([a]) 1-41 Cl methyl 2-fluoro-3-[rac-2,2-difluorocyclopropyl]phenyl hydroxy 1.82^([a]) 1-42 Cl methyl 2-fluoro-3-[rac-2,2-difluorocyclopropyl]phenyl isopropyloxy 4.23^([a]) 1-43 Cl H 2-fluoro-3-(1-fluorocyclopropyl)phenyl hydroxy 1.99^([a]) 1-44 Cl H 2-fluoro-3-(1-fluorocyclopropyl)phenyl isopropyloxy 4.62^([a]) 1-45 Cl methyl 2-fluoro-3-(1-fluorocyclopropyl)phenyl isopropyloxy 4.33^([a]) 1-46 methyl H 3-(difluoromethyl)-2-fluorophenyl hydroxy 1.43^([a])

TABLE 4 1-01: ¹H-NMR(400.1 MHz, d₆-DMSO): δ = 8.2400 (16.0); 7.6498 (2.3); 7.6302 (5.4); 7.6106 (3.8); 7.5151 (4.9); 7.4824 (7.4); 7.4627 (4.5); 7.4423 (3.4); 7.2113 (3.0); 7.0721 (6.5); 6.9329 (3.2); 2.5098 (2.1) 1-02: ¹H-NMR(499.9 MHz, d₆-DMSO): δ =7.2008 (0.5); 7.1974 (0.6); 7.1845 (1.3); 7.1815 (1.2); 7.1714 (1.3); 7.1667 (1.4); 7.1639 (2.1); 7.1483 (1.9); 7.1323 (0.7); 6.9341 (0.8); 6.9309 (0.8); 6.9188 (1.1); 6.9163 (1.2); 6.9061 (0.6); 6.9020 (0.5); 2.5135 (0.4); 2.5099 (0.5); 2.5063 (0.4); 2.3968 (16.0); 2.3846 (0.4); 2.0707 (0.6); 2.0641 (0.6); 2.0539 (1.1); 2.0436 (0.7); 2.0371 (0.6); 1.0253 (0.9); 1.0166 (2.2); 1.0122 (2.3); 1.0086 (1.3); 1.0039 (1.3); 0.9997 (2.2); 0.9953 (2.2); 0.9871 (0.9); 0.7823 (1.0); 0.7739 (2.4); 0.7720 (2.1); 0.7698 (2.5); 0.7637 (2.4); 0.7596 (2.5); 0.7507 (0.8) 1-03: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.5607 (0.9); 7.5349 (2.7); 7.5100 (2.2); 7.4700 (0.9); 7.4634 (1.4); 7.4561 (0.7); 7.4478 (0.5); 7.4453 (0.5); 7.4390 (0.7); 7.4323 (0.5); 7.4022 (1.8); 7.2986 (8.6); 5.3359 (5.0); 3.7789 (0.8); 3.6362 (3.8); 3.4357 (4.8); 3.2797 (1.0); 2.7276 (16.0); 1.6155 (15.9); 1.2931 (0.5); 0.9180 (0.4); 0.1060 (4.2); 0.0360 (5.0) 1-04: ¹H-NMR(300.2 MHz, d₆-DMSO): δ = 7.7747 (2.4); 7.7475 (8.1); 7.7204 (13.3); 7.7120 (13.1); 7.6924 (16.0); 7.6526 (0.5); 7.6169 (7.8); 7.5910 (5.1); 3.6770 (0.3); 3.6257 (0.3); 3.6165 (0.3); 3.5687 (0.4); 3.5321 (0.4); 3.4984 (0.4); 3.4631 (0.4); 3.4373 (0.4); 3.4027 (0.4); 3.3673 (0.4); 3.2814 (0.3); 3.2318 (0.3); 2.6507 (0.6); 2.5397 (13.4); 2.5340 (16.5); 2.4347 (75.8); 2.2151 (0.4); 2.1066 (1.0); 1.3861 (0.4); 1.2634 (1.1); 1.2122 (0.8); 0.0288 (8.6) 1-05: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.6445 (0.5); 7.5698 (2.7); 7.5445 (7.8); 7.5195 (16.0); 7.5093 (9.8); 7.4764 (11.2); 7.4396 (5.2); 7.4332 (8.1); 7.4263 (4.2); 7.4086 (5.5); 7.3826 (0.6); 7.3637 (0.7); 7.3254 (0.6); 7.3137 (0.6); 7.2986 (53.8); 7.2646 (0.4); 6.2623 (0.4); 6.1844 (3.5); 6.0638 (0.7); 6.0086 (0.3); 4.1995 (0.8); 4.1756 (2.3); 4.1519 (2.3); 4.1283 (0.8); 3.9955 (1.5); 3.7885 (5.4); 2.9593 (1.0); 2.9468 (2.0); 2.9363 (3.0); 2.9243 (4.0); 2.9173 (4.2); 2.9054 (2.9); 2.8954 (2.1); 2.8833 (1.1); 2.1754 (0.6); 2.0898 (11.2); 1.3210 (2.9); 1.2972 (5.9); 1.2734 (2.9); 1.2573 (0.8); 1.0060 (0.5); 0.9871 (0.6); 0.9703 (0.5); 0.9336 (2.4); 0.9096 (10.1); 0.8908 (10.0); 0.8686 (4.7); 0.8384 (1.8); 0.8233 (1.3); 0.8183 (1.3); 0.7839 (4.0); 0.7680 (10.0); 0.7601 (11.9); 0.7312 (2.6); 0.0482 (1.6); 0.0450 (0.8); 0.0374 (52.7); 0.0282 (1.7); 0.0265 (2.1) 1-06: ¹H-NMR(300.2 MHz, d₆-DMSO): δ = 8.2130 (16.0); 7.3593 (2.5); 7.3332 (5.6); 7.3070 (3.4); 7.0221 (3.3); 7.0179 (3.1); 7.0083 (2.7); 7.0051 (2.6); 7.0002 (5.0); 6.9971 (5.0); 6.9819 (1.8); 6.9786 (1.8); 6.9739 (3.5); 6.9708 (2.8); 6.9607 (4.6); 6.9548 (5.0); 6.9484 (2.6); 5.7756 (1.8); 2.5344 (1.4); 2.5284 (3.0); 2.5223 (4.1); 2.5162 (3.0); 2.5103 (1.4); 2.0139 (0.6); 2.0090 (0.4); 1.9970 (1.2); 1.9859 (1.4); 1.9807 (1.0); 1.9693 (2.6); 1.9578 (1.0); 1.9524 (1.5); 1.9414 (1.4); 1.9245 (0.7); 1.0128 (1.6); 0.9983 (4.4); 0.9908 (4.9); 0.9852 (2.4); 0.9772 (2.6); 0.9702 (4.7); 0.9628 (4.5); 0.9494 (2.0); 0.7347 (2.0); 0.7209 (5.0); 0.7178 (4.2); 0.7139 (5.2); 0.7044 (4.8); 0.6974 (5.3); 0.6822 (1.6); 0.0194 (4.1) 1-07: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.5660 (0.9); 7.5561 (3.4); 7.5510 (2.4); 7.5352 (2.5); 7.5283 (2.4); 7.5127 (0.7); 7.4844 (2.5); 7.4365 (1.2); 7.4331 (1.7); 7.4293 (1.1); 7.4207 (0.9); 7.4177 (1.2); 7.4143 (0.8); 7.3066 (0.4); 4.0134 (0.5); 4.0012 (1.2); 3.9889 (1.6); 3.9767 (1.2); 3.9644 (0.5); 3.6270 (7.7); 3.3918 (8.4); 1.9661 (0.7); 1.1838 (15.7); 1.1790 (0.7); 1.1715 (16.0); −0.0002 (0.4) 1-08: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9376 (5.4); 7.6355 (0.5); 7.5766 (0.4); 7.5552 (0.8); 7.5345 (0.5); 7.5325 (0.5); 7.5089 (0.4); 7.5061 (0.4); 7.4818 (0.9); 7.4792 (0.8); 7.4575 (0.6); 7.4549 (0.6); 7.3709 (0.8); 7.3437 (1.2); 7.3177 (0.4); 7.2984 (2.8); 7.1103 (0.9); 6.9278 (1.8); 6.7452 (0.9); 5.4078 (0.4); 5.3870 (1.0); 5.3661 (1.3); 5.3452 (1.0); 5.3244 (0.4); 1.6170 (0.8); 1.4798 (1.5); 1.4609 (16.0); 1.4400 (15.1); 1.4256 (0.5); 1.4046 (0.4); 1.2465 (0.4); 0.0361 (2.9) 1-09: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.5541 (0.4); 7.5433 (0.9); 7.5165 (2.2); 7.5102 (1.3); 7.4902 (1.5); 7.4883 (1.4); 7.4831 (1.6); 7.4402 (0.7); 7.4327 (1.2); 7.4255 (0.6); 7.4169 (0.4); 7.4144 (0.4); 7.4090 (0.6); 7.4018 (0.3); 7.2985 (2.8); 5.6931 (0.8); 4.0184 (1.9); 4.0071 (0.4); 3.9923 (16.0); 2.7929 (0.4); 2.7891 (0.4); 2.7825 (0.4); 2.7771 (0.6); 2.7705 (0.7); 2.7651 (0.5); 2.7585 (0.4); 2.7550 (0.4); 2.7483 (0.4); 2.0802 (0.7); 1.6331 (0.7); 1.2941 (0.4); 0.8795 (1.4); 0.8742 (0.9); 0.8618 (1.4); 0.8570 (1.2); 0.8517 (0.9); 0.8395 (0.7); 0.8107 (0.4); 0.7720 (0.7); 0.7589 (1.5); 0.7490 (1.5); 0.7455 (1.5); 0.7325 (0.8); 0.7197 (0.3); 0.0350 (2.4) 1-10: ¹H-NMR(499.9 MHz, d₆-DMSO): δ = 8.2502 (16.0); 8.0080 (1.2); 7.2221 (0.5); 7.2063 (1.3); 7.2027 (1.4); 7.1899 (3.5); 7.1868 (3.2); 7.1767 (7.8); 7.1620 (5.1); 7.1458 (1.7); 6.9476 (2.0); 6.9442 (2.1); 6.9334 (2.8); 6.9290 (3.0); 6.9209 (1.5); 6.9154 (1.3); 2.5087 (2.8); 2.5051 (3.7); 2.5016 (2.6); 2.0890 (0.9); 2.0788 (1.6); 2.0720 (1.8); 2.0620 (2.9); 2.0519 (1.7); 2.0452 (1.5); 2.0348 (0.7); 1.9900 (0.6); 1.1759 (0.4); 1.0341 (2.4); 1.0255 (5.8); 1.0211 (5.8); 1.0175 (3.2); 1.0127 (3.3); 1.0086 (5.4); 1.0042 (5.4); 0.9960 (2.0); 0.8237 (0.4); 0.8130 (0.5); 0.7937 (2.7); 0.7854 (6.6); 0.7813 (6.5); 0.7753 (6.2); 0.7712 (6.0); 0.7622 (1.8) 1-11: ¹H-NMR(300.2 MHz, d₆-DMSO): δ = 8.0139 (9.2); 7.7429 (0.8); 7.7169 (2.4); 7.6915 (2.4); 7.6678 (3.0); 7.6430 (4.7); 7.5644 (2.0); 7.5380 (1.5); 3.0021 (1.8); 2.9768 (5.6); 2.9515 (5.7); 2.9263 (1.9); 2.5341 (2.3); 2.5281 (4.7); 2.5221 (6.5); 2.5161 (4.7); 2.5102 (2.2); 2.0085 (0.5); 1.9290 (0.4); 1.3136 (7.2); 1.2884 (16.0); 1.2631 (6.9); 0.0182 (7.1); −0.0419 (1.3) 1-12: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.7672 (4.6); 7.5697 (1.0); 7.5431 (1.7); 7.5290 (2.2); 7.5215 (1.8); 7.4764 (0.8); 7.4707 (1.1); 7.4641 (0.7); 7.4453 (0.7); 7.2990 (5.2); 5.3887 (0.4); 5.3679 (1.0); 5.3470 (1.3); 5.3261 (1.0); 5.3053 (0.4); 3.1003 (1.0); 3.0749 (3.3); 3.0496 (3.4); 3.0243 (1.2); 1.6181 (9.2); 1.4489 (4.2); 1.4341 (16.0); 1.4236 (8.8); 1.4132 (15.9); 1.3982 (3.9); 0.1066 (1.2); 0.0359 (4.9) 1-13: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.9312 (0.5); 8.7218 (5.7); 7.6865 (0.4); 7.6605 (1.5); 7.6368 (4.5); 7.6136 (0.6); 7.5818 (2.3); 7.5362 (1.0); 7.5285 (1.6); 7.5213 (0.9); 7.5058 (1.0); 7.2986 (8.3); 7.1162 (0.3); 4.1844 (0.7); 4.1606 (0.8); 3.8821 (0.4); 2.8702 (16.0); 2.6686 (1.2); 2.1970 (2.5); 2.1014 (3.4); 1.9497 (0.5); 1.6815 (0.4); 1.4679 (0.4); 1.4314 (0.3); 1.4067 (0.5); 1.3816 (0.5); 1.3593 (0.8); 1.3319 (0.6); 1.3261 (1.1); 1.3023 (2.0); 1.2902 (0.4); 1.2784 (1.0); 0.9825 (1.0); 0.9582 (1.8); 0.9340 (0.8); 0.1065 (0.7); 0.0352 (8.0); 0.0243 (0.4) 1-14: ¹H-NMR(400.1 MHz, d₆-DMSO): δ = 8.0394 (5.5); 7.7256 (0.6); 7.7063 (1.9); 7.6866 (1.6); 7.6542 (2.3); 7.6331 (3.8); 7.5609 (1.6); 7.5403 (1.4); 3.9145 (16.0); 3.3269 (11.0); 2.6442 (15.2); 2.5097 (1.8) 1-15: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.0165 (5.2); 7.5853 (1.0); 7.5593 (2.0); 7.5527 (1.6); 7.5470 (1.9); 7.5370 (1.8); 7.4918 (0.7); 7.4850 (1.1); 7.4782 (0.6); 7.4654 (0.4); 7.4598 (0.6); 7.2985 (4.6); 7.1094 (1.0); 7.0725 (1.2); 7.0501 (1.2); 7.0133 (1.2); 6.2880 (2.3); 6.2288 (2.0); 5.7406 (2.3); 5.7037 (2.1); 5.4053 (0.4); 5.3845 (1.0); 5.3636 (1.4); 5.3427 (1.0); 5.3219 (0.4); 1.6133 (1.8); 1.4481 (16.0); 1.4272 (15.8); 0.0363 (4.3) 1-16: ¹H-NMR(400.1 MHz, d₆-DMSO): δ = 7.8912 (5.7); 7.3097 (1.3); 7.2902 (2.8); 7.2706 (1.7); 6.9569 (2.0); 6.9376 (1.9); 6.9046 (1.9); 6.8752 (3.4); 2.6079 (16.0); 2.5101 (2.7); 1.9793 (0.3); 1.9665 (0.7); 1.9580 (0.9); 1.9458 (1.4); 1.9335 (1.0); 1.9250 (0.9); 1.9123 (0.4); 0.9823 (0.8); 0.9712 (2.4); 0.9660 (2.8); 0.9504 (2.7); 0.9453 (2.8); 0.9351 (1.2); 0.7049 (1.0); 0.6935 (3.0); 0.6899 (3.2); 0.6818 (3.0); 0.6774 (3.3); 0.6659 (1.0) 1-17: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.8520 (4.3); 7.5819 (0.6); 7.5583 (1.4); 7.5372 (1.4); 7.5170 (0.7); 7.3531 (0.7); 7.3263 (1.1); 7.2986 (2.2); 4.0423 (16.0); 2.7528 (14.2); 1.2898 (0.5); 0.0335 (1.6) 1-18: ¹H-NMR(300.2 MHz, d₆-DMSO): δ = 8.2409 (16.0); 8.1115 (0.6); 7.9405 (1.1); 7.8747 (1.8); 7.8503 (3.7); 7.8227 (2.3); 7.8127 (2.0); 7.7868 (3.6); 7.7656 (2.3); 7.5853 (2.5); 7.5587 (4.1); 7.5321 (1.8); 4.1145 (0.5); 4.0839 (0.4); 4.0726 (1.0); 4.0489 (1.0); 3.5064 (0.4); 3.3515 (0.6); 3.3099 (0.5); 3.0723 (1.7); 3.0521 (0.7); 3.0411 (0.5); 3.0096 (0.3); 2.9228 (1.8); 2.8928 (0.7); 2.8579 (0.4); 2.7637 (1.5); 2.5463 (9.6); 2.5404 (20.1); 2.5343 (27.5); 2.5283 (19.6); 2.5224 (9.0); 2.0211 (3.9); 1.3872 (0.8); 1.2914 (0.5); 1.2660 (1.1); 1.2300 (1.3); 1.2062 (2.6); 1.2012 (1.1); 1.1825 (1.2); 0.1641 (0.4); 0.1162 (0.4); 0.0419 (0.5); 0.0310 (14.4); 0.0201 (0.6) 1-19: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.9753 (5.2); 7.6683 (0.6); 7.5512 (0.8); 7.5390 (1.8); 7.5259 (2.2); 7.5122 (1.1); 7.3323 (1.0); 7.3162 (1.8); 7.3001 (0.8); 7.2636 (1.5); 7.0994 (0.4); 4.0289 (16.0); 3.1503 (0.4); 2.9572 (1.4); 2.9112 (0.4); 2.8836 (1.2); −0.0002 (1.2) 1-20: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.5717 (0.3); 7.5706 (0.3); 7.5562 (1.2); 7.5436 (3.3); 7.4786 (1.5); 7.4294 (0.6); 7.4239 (1.1); 7.4197 (0.8); 7.4157 (0.5); 7.4107 (0.7); 7.4065 (0.4); 7.2606 (2.2); 4.1428 (0.3); 4.0748 (1.1); 4.0582 (16.0); 3.9978 (0.3); 1.5556 (2.7); −0.0002 (2.2) 1-21: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.8995 (5.5); 7.5887 (0.6); 7.2987 (3.4); 7.1384 (0.3); 7.1201 (1.3); 7.1163 (1.4); 7.1109 (2.2); 7.0931 (3.4); 7.0661 (0.3); 6.8539 (0.6); 6.8451 (0.7); 6.8314 (1.0); 6.8215 (0.8); 6.8166 (1.1); 6.8003 (0.4); 5.4035 (0.4); 5.3827 (1.0); 5.3618 (1.4); 5.3409 (1.0); 5.3201 (0.4); 2.1478 (0.4); 2.1369 (0.5); 2.1304 (0.4); 2.1196 (0.9); 2.1087 (0.4); 2.1021 (0.6); 2.0914 (0.5); 1.6022 (2.8); 1.4751 (1.8); 1.4579 (16.0); 1.4371 (15.5); 1.0643 (0.7); 1.0492 (1.6); 1.0423 (1.7); 1.0362 (0.9); 1.0329 (0.7); 1.0275 (1.2); 1.0206 (1.8); 1.0138 (1.6); 0.9993 (0.9); 0.8139 (0.8); 0.7990 (1.9); 0.7929 (1.8); 0.7818 (1.8); 0.7764 (1.9); 0.7645 (0.6); 0.7597 (0.9); 0.7476 (0.4); 0.7418 (0.4); 0.0381 (3.4) 1-22: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.8527 (4.8); 7.8448 (0.7); 7.4713 (1.5); 7.3465 (0.9); 7.3329 (0.6); 7.3203 (1.7); 7.3065 (0.4); 7.2983 (1.8); 7.2940 (1.3); 7.0217 (1.2); 7.0137 (1.9); 7.0082 (1.4); 6.9977 (1.0); 6.9945 (1.0); 6.9866 (1.6); 6.9832 (1.3); 6.9467 (1.3); 6.9404 (1.7); 6.9331 (1.1); 6.9253 (0.5); 5.3803 (0.4); 5.3706 (0.3); 5.3595 (1.0); 5.3497 (0.4); 5.3387 (1.3); 5.3309 (0.7); 5.3178 (1.0); 5.2970 (0.4); 1.9690 (0.5); 1.9576 (0.5); 1.9410 (0.9); 1.9242 (0.5); 1.9131 (0.5); 1.6409 (2.4); 1.4629 (2.6); 1.4591 (4.6); 1.4361 (16.0); 1.4151 (14.5); 1.4033 (0.6); 1.3822 (0.4); 1.0347 (0.9); 1.0296 (0.6); 1.0194 (1.5); 1.0125 (1.7); 1.0096 (1.3); 0.9978 (1.0); 0.9910 (1.6); 0.9847 (1.4); 0.9697 (0.8); 0.7664 (0.9); 0.7513 (2.3); 0.7453 (2.0); 0.7348 (1.8); 0.7290 (2.4); 0.7126 (0.7); 0.0368 (1.6) 1-23: ¹H-NMR(300.2 MHz, d₆-DMSO): δ = 8.3083 (0.5); 8.3008 (16.0); 8.2931 (0.5); 8.0538 (0.7); 7.7123 (1.1); 7.6854 (2.4); 7.6603 (1.4); 7.6429 (1.1); 7.6185 (2.3); 7.5975 (1.6); 7.4964 (2.2); 7.4816 (2.6); 7.4699 (3.2); 7.4433 (1.2); 7.3016 (5.2); 7.1217 (2.6); 4.1088 (2.0); 2.5343 (1.6); 2.5284 (3.4); 2.5223 (4.6); 2.5162 (3.4); 2.5104 (1.6); 2.0075 (1.0); 1.1924 (0.6); 0.0159 (4.0) 1-24: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.2986 (6.2); 7.1237 (0.4); 7.1045 (1.4); 7.0965 (2.2); 7.0911 (2.7); 7.0769 (1.8); 7.0728 (2.5); 7.0454 (0.5); 6.8423 (0.3); 6.8363 (0.7); 6.8284 (0.8); 6.8208 (0.5); 6.8141 (1.1); 6.8033 (0.8); 6.7976 (0.8); 6.7828 (0.5); 5.8161 (0.4); 5.4585 (0.4); 5.4377 (1.0); 5.4168 (1.4); 5.3959 (1.1); 5.3751 (0.4); 2.6527 (8.2); 2.4601 (15.6); 2.4508 (2.3); 2.1444 (0.5); 2.1331 (0.6); 2.1162 (1.0); 2.0996 (0.7); 2.0878 (0.6); 2.0711 (0.3); 1.6184 (0.6); 1.4808 (1.7); 1.4701 (0.6); 1.4552 (16.0); 1.4343 (15.6); 1.4130 (0.5); 1.3921 (0.4); 1.2935 (0.4); 1.0594 (0.8); 1.0441 (1.9); 1.0373 (2.0); 1.0312 (1.4); 1.0226 (1.5); 1.0155 (2.0); 1.0091 (1.8); 0.9945 (1.1); 0.8051 (1.0); 0.7901 (2.2); 0.7840 (2.1); 0.7732 (2.0); 0.7670 (2.3); 0.7574 (0.7); 0.7509 (0.8); 0.7410 (0.5); 0.1079 (1.1); 0.0374 (5.2) 1-25: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.1443 (5.2); 7.5649 (0.5); 7.5494 (1.7); 7.5338 (2.0); 7.5254 (2.4); 7.5099 (0.9); 7.4936 (2.5); 7.4298 (1.5); 7.4146 (1.2); 7.2672 (0.5); 5.3302 (0.5); 5.3177 (1.2); 5.3052 (1.6); 5.2927 (1.2); 5.2802 (0.5); 1.6345 (0.4); 1.4002 (15.4); 1.3876 (16.0); −0.0002 (0.5) 1-26: ¹H-NMR(499.9 MHz, d₆-DMSO): δ = 8.0179 (6.6); 7.7953 (0.7); 7.7804 (1.4); 7.7656 (0.8); 7.7208 (0.7); 7.7069 (1.2); 7.6936 (0.8); 7.5189 (1.0); 7.5027 (1.6); 7.4865 (0.7); 2.6214 (16.0); 2.5058 (0.4); 1.3515 (0.9) 1-27: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 7.7089 (0.7); 7.6892 (2.0); 7.6694 (1.7); 7.6395 (2.0); 7.6200 (1.1); 7.5614 (2.6); 7.5153 (1.4); 7.4954 (1.1); 2.5592 (16.4); 2.5156 (2.0); 2.5112 (4.2); 2.5069 (5.7); 2.5024 (4.1); 2.4983 (2.0); 2.3154 (0.5); 2.3022 (16.0); 0.0008 (4.3) 1-28: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.2043 (5.1); 7.5859 (1.0); 7.5595 (2.0); 7.5517 (1.6); 7.5471 (1.5); 7.5332 (2.0); 7.4915 (0.8); 7.4854 (1.1); 7.4788 (0.6); 7.4604 (0.6); 7.2986 (5.3); 5.6409 (2.3); 5.6325 (2.4); 5.4040 (0.4); 5.3831 (1.0); 5.3623 (1.4); 5.3414 (1.0); 5.3205 (0.4); 4.5051 (2.0); 4.4967 (2.0); 4.0863 (0.9); 4.0630 (3.0); 4.0397 (3.1); 4.0164 (1.0); 1.5943 (5.2); 1.5232 (3.4); 1.5000 (7.1); 1.4767 (3.4); 1.4479 (16.0); 1.4270 (15.8); 1.4090 (0.3); 1.3594 (0.3); 0.9838 (0.4); 0.9596 (0.8); 0.9353 (0.3); 0.1073 (0.3); 0.0366 (5.2) 1-29: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.5419 (5.5); 7.6428 (1.0); 7.6180 (2.9); 7.6128 (1.5); 7.5942 (0.4); 7.5693 (1.4); 7.5279 (0.7); 7.5201 (1.2); 7.5129 (0.6); 7.5057 (0.4); 7.5029 (0.4); 7.4971 (0.6); 7.4897 (0.4); 7.2985 (4.3); 5.4235 (0.4); 5.4026 (1.0); 5.3817 (1.4); 5.3609 (1.0); 5.3400 (0.4); 2.8544 (16.0); 1.6014 (4.4); 1.4677 (15.6); 1.4468 (15.8); 1.4331 (0.4); 1.4255 (0.6); 1.4068 (0.3); 1.3583 (0.5); 1.3309 (0.4); 0.9821 (0.6); 0.9579 (1.2); 0.9336 (0.5); 0.1058 (0.5); 0.0345 (4.0) 1-30: ¹H-NMR(499.9 MHz, d₆-DMSO): δ = 7.9572 (6.3); 7.1617 (0.3); 7.1570 (0.4); 7.1478 (3.0); 7.1410 (1.9); 7.1387 (1.9); 7.1330 (2.8); 6.9088 (0.7); 6.9020 (0.7); 6.8961 (1.2); 6.8896 (1.1); 6.8827 (0.6); 6.8765 (0.5); 2.7404 (0.9); 2.6089 (16.0); 2.5168 (0.3); 2.5134 (0.6); 2.5098 (0.8); 2.5062 (0.6); 2.0661 (0.6); 2.0596 (0.7); 2.0494 (1.2); 2.0424 (0.5); 2.0391 (0.7); 2.0326 (0.6); 1.0221 (0.9); 1.0134 (2.3); 1.0091 (2.4); 1.0053 (1.3); 1.0007 (1.4); 0.9965 (2.2); 0.9922 (2.3); 0.9840 (0.9); 0.7812 (1.0); 0.7729 (2.5); 0.7706 (2.3); 0.7689 (2.6); 0.7627 (2.5); 0.7587 (2.5); 0.7498 (0.8) 1-31: ¹H-NMR(400.1 MHz, CDCl3): δ = 7.5310 (0.4); 7.5109 (1.2); 7.4911 (1.8); 7.4829 (1.9); 7.4692 (2.3); 7.4189 (1.2); 7.3997 (0.7); 7.2594 (7.0); 3.9970 (16.0); 2.6349 (13.6); 2.3177 (13.5); 1.5482 (6.2); −0.0002 (6.0) 1-32: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9240 (16.0); 7.6334 (0.9); 7.6078 (3.4); 7.5830 (11.0); 7.5582 (1.3); 7.5351 (5.3); 7.5109 (0.6); 7.4887 (2.3); 7.4814 (3.8); 7.4742 (2.2); 7.4641 (1.5); 7.4581 (2.4); 7.3042 (16.9); 5.4053 (1.2); 5.3845 (3.1); 5.3636 (4.1); 5.3428 (3.1); 5.3220 (1.3); 3.2115 (0.5); 3.0865 (0.6); 1.6662 (0.7); 1.6272 (3.0); 1.4829 (4.0); 1.4561 (47.2); 1.4352 (46.6); 1.4148 (1.2); 1.4098 (1.0); 1.3939 (1.0); 1.3890 (0.9); 1.2961 (1.1); 1.2429 (0.4); 1.2215 (0.3); 0.1139 (0.4); 0.0523 (0.6); 0.0415 (15.6); 0.0307 (0.6) 1-33: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.5580 (0.4); 7.5425 (1.5); 7.5268 (3.1); 7.5088 (0.6); 7.4751 (2.1); 7.4226 (1.3); 7.4079 (1.0); 7.2602 (3.1); 4.0240 (16.0); 2.4323 (15.4); 1.5511 (4.0); −0.0002 (3.2) 1-34: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.6515 (4.6); 8.6433 (4.4); 8.1431 (16.0); 8.0830 (0.7); 8.0735 (0.9); 8.0629 (5.2); 8.0538 (5.0); 8.0328 (1.6); 7.8430 (1.9); 7.2989 (30.5); 5.6864 (0.3); 5.6319 (0.3); 5.6114 (0.3); 4.2139 (0.5); 4.1900 (1.7); 4.1662 (1.7); 4.1424 (0.6); 2.2125 (0.5); 2.1079 (8.1); 1.3303 (2.2); 1.3065 (4.4); 1.2932 (0.5); 1.2827 (2.2); 0.1072 (4.5); 0.0480 (1.1); 0.0371 (32.3); 0.0263 (1.2) 1-35: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.5958 (2.6); 8.5877 (2.5); 8.0485 (0.4); 8.0394 (0.5); 8.0248 (3.6); 8.0199 (11.4); 7.8867 (0.8); 7.6915 (1.2); 7.2987 (16.5); 5.3377 (0.8); 4.5648 (2.2); 4.5550 (1.1); 4.5410 (7.0); 4.5310 (1.5); 4.5172 (7.1); 4.5070 (1.0); 4.4935 (2.3); 1.5921 (15.2); 1.5188 (0.9); 1.5025 (7.9); 1.4950 (2.2); 1.4787 (16.0); 1.4714 (1.5); 1.4549 (7.6); 1.2911 (0.4); 0.1061 (0.7); 0.0470 (0.6); 0.0361 (16.8); 0.0252 (0.6) 1-36: ¹H-NMR(300.2 MHz, d₆-DMSO): δ = 8.7017 (1.3); 8.6952 (1.5); 8.6861 (6.0); 8.6850 (5.6); 8.6797 (6.3); 8.6674 (1.4); 8.6596 (1.4); 8.6268 (5.9); 8.6189 (6.2); 8.3059 (16.0); 8.2818 (0.9); 8.2749 (1.4); 8.2674 (0.8); 8.2297 (4.5); 8.2230 (6.4); 8.2154 (4.1); 8.1457 (0.4); 8.0647 (0.3); 8.0472 (3.3); 5.7778 (0.4); 4.0597 (0.5); 4.0360 (0.4); 3.1873 (0.4); 2.5611 (14.4); 2.5339 (3.5); 2.5279 (7.4); 2.5218 (10.0); 2.5158 (7.2); 2.5099 (3.3); 2.0085 (1.8); 1.9286 (1.0); 1.2173 (0.5); 1.1936 (1.0); 1.1698 (0.5); 0.0294 (0.5); 0.0186 (13.5); 0.0093 (0.4); 0.0076 (0.5) 1-37: ¹H-NMR(300.2 MHz, d₆-DMSO): δ = 8.2172 (16.0); 7.8172 (1.1); 7.5335 (0.4); 7.5209 (2.7); 7.5083 (1.1); 7.4950 (5.9); 7.4813 (1.3); 7.4687 (4.0); 7.4323 (0.4); 7.2414 (0.8); 7.2065 (8.3); 7.1989 (5.9); 7.1802 (5.2); 7.1726 (5.8); 7.1660 (6.8); 7.1604 (6.4); 5.7866 (0.5); 5.5279 (0.3); 5.4410 (0.6); 5.2844 (0.6); 4.0613 (0.8); 4.0377 (0.8); 4.0142 (0.4); 3.6447 (0.3); 3.3505 (11.6); 3.2182 (0.8); 3.1169 (0.4); 2.7483 (0.5); 2.5853 (0.4); 2.5346 (21.8); 2.5287 (46.6); 2.5227 (64.6); 2.5167 (46.8); 2.5108 (21.7); 2.2933 (0.4); 2.0100 (3.1); 1.9297 (5.9); 1.7140 (0.4); 1.5738 (1.3); 1.5537 (4.9); 1.5468 (4.9); 1.5277 (1.9); 1.5086 (1.4); 1.4880 (4.7); 1.4816 (5.0); 1.4631 (2.0); 1.3997 (0.4); 1.2828 (0.4); 1.2537 (2.2); 1.2318 (5.2); 1.2236 (6.3); 1.2011 (6.3); 1.1951 (6.3); 1.1713 (2.0); 0.2153 (0.4); 0.0318 (2.5); 0.0208 (76.8); 0.0098 (2.6) 1-38: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.8774 (4.8); 7.8763 (4.8); 7.5175 (0.7); 7.4681 (0.7); 7.4420 (1.6); 7.4164 (0.9); 7.2999 (5.3); 7.2987 (5.2); 7.1733 (4.2); 7.1458 (2.4); 7.1188 (1.3); 5.3926 (0.4); 5.3715 (1.0); 5.3635 (0.4); 5.3507 (1.3); 5.3300 (1.2); 5.3091 (0.4); 1.5965 (4.9); 1.5767 (1.5); 1.5715 (1.5); 1.5498 (0.6); 1.5350 (0.6); 1.5130 (1.6); 1.5078 (1.6); 1.4867 (0.7); 1.4693 (2.5); 1.4462 (16.0); 1.4250 (14.6); 1.4046 (0.4); 1.1657 (0.6); 1.1437 (1.7); 1.1387 (2.1); 1.1150 (2.0); 1.1095 (1.8); 1.0871 (0.5); 0.0391 (7.1); 0.0378 (6.9) 1-39: ¹H-NMR(300.2 MHz, d₆-DMSO): δ = 8.2768 (16.0); 7.4354 (1.2); 7.4196 (2.2); 7.4107 (1.5); 7.4026 (2.9); 7.3861 (1.8); 7.3781 (1.9); 7.3314 (1.5); 7.3053 (8.5); 7.2868 (6.3); 7.2596 (0.6); 7.2507 (0.4); 3.1586 (0.9); 3.1303 (1.2); 3.1189 (1.7); 3.0879 (1.7); 3.0500 (1.0); 2.5338 (2.8); 2.5279 (5.7); 2.5219 (7.5); 2.5158 (5.4); 2.5100 (2.6); 2.1738 (0.4); 2.1459 (1.0); 2.1356 (0.7); 2.1246 (1.3); 2.1079 (2.6); 2.0856 (2.4); 2.0732 (2.9); 2.0612 (1.6); 2.0469 (2.2); 2.0323 (1.4); 2.0196 (0.5); 1.9291 (12.3); 0.0183 (5.8) 1-40: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9179 (6.4); 7.6094 (0.4); 7.2986 (12.0); 7.2758 (0.9); 7.2703 (0.8); 7.2528 (0.8); 7.2468 (0.8); 7.2235 (0.9); 7.1975 (1.4); 7.1945 (1.4); 7.1706 (0.7); 7.1679 (0.8); 7.1405 (0.6); 7.1375 (0.6); 7.1348 (0.6); 7.1165 (0.8); 7.1141 (0.7); 5.4071 (0.4); 5.3862 (1.1); 5.3653 (1.4); 5.3445 (1.1); 5.3236 (0.4); 2.9082 (0.3); 2.8949 (0.6); 2.8677 (0.6); 2.8544 (0.3); 2.8268 (0.3); 1.9830 (0.3); 1.9734 (0.4); 1.9603 (0.6); 1.9564 (0.5); 1.9434 (0.6); 1.9339 (0.7); 1.9207 (0.4); 1.9168 (0.7); 1.8944 (0.4); 1.8772 (0.3); 1.7473 (0.3); 1.7342 (0.4); 1.7204 (0.6); 1.7069 (0.8); 1.6927 (0.6); 1.6785 (0.7); 1.6652 (0.6); 1.6511 (0.4); 1.5844 (7.9); 1.4782 (1.3); 1.4618 (16.0); 1.4409 (15.7); 0.0481 (0.4); 0.0433 (0.4); 0.0374 (14.2); 0.0297 (0.4); 0.0280 (0.4); 0.0265 (0.5) 1-41: ¹H-NMR(300.2 MHz, d₆-DMSO): δ = 8.2790 (2.3); 7.4340 (0.6); 7.4198 (2.0); 7.4024 (3.7); 7.3950 (2.2); 7.3866 (4.6); 7.3720 (2.9); 7.3623 (3.1); 7.3269 (1.8); 7.3015 (16.0); 7.2845 (9.6); 7.2771 (8.0); 7.2585 (1.1); 3.6128 (0.3); 3.5872 (0.4); 3.3811 (0.8); 3.3129 (0.7); 3.2895 (0.7); 3.1978 (0.4); 3.1540 (1.7); 3.1237 (2.2); 3.1138 (3.0); 3.0836 (3.1); 3.0453 (1.9); 2.9110 (2.3); 2.7518 (2.1); 2.7092 (1.2); 2.5340 (13.1); 2.5280 (28.4); 2.5219 (39.3); 2.5158 (28.3); 2.5100 (13.3); 2.4263 (55.4); 2.4070 (3.8); 2.3600 (0.4); 2.2074 (0.4); 2.1720 (0.7); 2.1441 (1.7); 2.1347 (1.0); 2.1229 (2.1); 2.1062 (4.3); 2.0840 (4.2); 2.0712 (5.1); 2.0587 (2.6); 2.0447 (3.8); 2.0300 (2.4); 2.0159 (0.8); 2.0093 (1.0); 2.0035 (0.5); 1.9289 (1.1); 0.0307 (1.7); 0.0290 (0.9); 0.0275 (1.2); 0.0199 (53.0); 0.0122 (1.8); 0.0107 (1.8); 0.0090 (1.9) 1-42: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9172 (0.6); 7.2981 (5.1); 7.2842 (0.6); 7.2625 (1.2); 7.2397 (0.9); 7.2341 (1.0); 7.2004 (1.0); 7.1740 (1.8); 7.1470 (1.0); 7.1173 (1.0); 7.0966 (1.1); 7.0713 (0.4); 5.4608 (0.4); 5.4399 (1.1); 5.4190 (1.4); 5.3981 (1.1); 5.3773 (0.4); 2.9312 (0.4); 2.9033 (0.5); 2.8906 (0.8); 2.8629 (0.9); 2.8501 (0.5); 2.8224 (0.5); 2.4670 (16.0); 2.4551 (1.6); 2.2082 (8.2); 1.9938 (0.3); 1.9766 (0.4); 1.9673 (0.4); 1.9540 (0.7); 1.9371 (0.7); 1.9278 (0.7); 1.9110 (0.8); 1.8974 (0.4); 1.8882 (0.4); 1.8710 (0.4); 1.7393 (0.4); 1.7261 (0.4); 1.7122 (0.6); 1.6988 (0.9); 1.6847 (0.7); 1.6707 (0.9); 1.6571 (0.7); 1.6434 (0.4); 1.6300 (0.3); 1.6007 (4.9); 1.4817 (1.2); 1.4683 (1.5); 1.4570 (14.6); 1.4361 (14.0); 1.2956 (0.5); 0.9183 (0.4); 0.0361 (3.6) 1-43: ¹H-NMR(300.2 MHz, d₆-DMSO): δ = 8.2836 (1.4); 8.2772 (16.0); 8.0256 (0.8); 7.5855 (0.4); 7.5487 (1.7); 7.5442 (1.5); 7.5229 (3.8); 7.5103 (3.4); 7.5049 (3.4); 7.4983 (2.9); 7.4936 (2.4); 7.4892 (2.2); 7.4835 (2.2); 7.3768 (2.8); 7.3503 (3.9); 7.3238 (1.6); 4.0603 (0.6); 4.0366 (0.6); 3.3605 (1.2); 3.2371 (0.6); 2.5342 (7.1); 2.5283 (15.8); 2.5223 (22.2); 2.5162 (16.4); 2.5104 (7.8); 2.0093 (2.6); 1.9292 (7.7); 1.5028 (1.0); 1.4759 (3.9); 1.4545 (1.6); 1.4402 (1.2); 1.4132 (4.0); 1.3921 (1.8); 1.2548 (0.4); 1.2247 (1.6); 1.2181 (1.1); 1.2027 (4.2); 1.1948 (5.8); 1.1732 (5.1); 1.1443 (1.2); 0.0302 (0.7); 0.0194 (25.5); 0.0085 (1.1) 1-44: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9261 (0.4); 7.9166 (5.3); 7.6145 (0.4); 7.4855 (0.3); 7.4803 (0.5); 7.4756 (0.4); 7.4594 (0.9); 7.4543 (1.0); 7.4502 (0.6); 7.4386 (0.5); 7.4333 (0.6); 7.4286 (0.5); 7.3637 (0.4); 7.3600 (0.4); 7.3388 (1.0); 7.3366 (0.9); 7.3154 (0.8); 7.3128 (0.7); 7.3095 (0.7); 7.2990 (4.7); 7.2686 (1.1); 7.2422 (1.3); 7.2156 (0.5); 7.0516 (1.2); 7.0471 (0.8); 7.0317 (0.7); 7.0277 (0.4); 5.4051 (0.4); 5.3843 (1.0); 5.3634 (1.4); 5.3425 (1.0); 5.3217 (0.4); 5.2848 (0.6); 5.2686 (0.6); 1.6046 (3.3); 1.5156 (0.5); 1.4927 (1.6); 1.4894 (1.6); 1.4769 (1.7); 1.4597 (16.0); 1.4388 (15.7); 1.4037 (0.7); 1.3039 (1.0); 1.2341 (0.6); 1.2131 (1.4); 1.2057 (1.6); 1.1833 (1.7); 1.1758 (1.3); 1.1636 (0.5); 1.1557 (0.8); 1.1340 (0.5); 1.1287 (0.4); 0.9410 (0.3); 0.9194 (1.1); 0.8961 (0.4); 0.0375 (6.0) 1-45: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.4720 (0.4); 7.4670 (0.6); 7.4621 (0.4); 7.4457 (0.9); 7.4409 (1.0); 7.4252 (0.5); 7.4199 (0.6); 7.4152 (0.5); 7.3599 (0.3); 7.3545 (0.4); 7.3508 (0.4); 7.3296 (0.9); 7.3275 (0.9); 7.2991 (13.2); 7.2490 (0.9); 7.2224 (1.2); 7.1957 (0.5); 7.0557 (1.4); 7.0506 (1.0); 7.0353 (0.7); 7.0309 (0.4); 5.4608 (0.4); 5.4399 (1.0); 5.4191 (1.3); 5.3982 (1.0); 5.3773 (0.4); 5.2403 (0.8); 5.2239 (0.8); 2.4655 (15.5); 2.4545 (1.8); 1.5914 (11.8); 1.5121 (0.4); 1.4898 (1.6); 1.4817 (2.4); 1.4570 (16.0); 1.4361 (15.8); 1.4231 (1.7); 1.4001 (0.6); 1.3042 (1.3); 1.2301 (0.6); 1.2093 (1.4); 1.2019 (1.6); 1.1796 (1.6); 1.1717 (1.4); 1.1587 (0.6); 1.1516 (0.5); 1.1363 (0.6); 0.9417 (0.5); 0.9200 (1.4); 0.8966 (0.6); 0.0489 (0.5); 0.0380 (16.4); 0.0270 (0.6) 1-46: ¹H-NMR(300.2 MHz, d₆-DMSO): δ = 14.2022 (0.6); 8.7327 (0.4); 8.0182 (16.0); 7.6607 (1.6); 7.6333 (3.2); 7.6098 (3.3); 7.5871 (3.0); 7.5663 (2.2); 7.4954 (0.4); 7.4753 (3.5); 7.4691 (3.9); 7.4488 (4.2); 7.4232 (1.6); 7.2887 (6.9); 7.1086 (3.4); 4.1060 (0.6); 4.0607 (0.8); 4.0369 (0.7); 3.5879 (2.3); 3.3496 (11.3); 2.7485 (0.3); 2.6346 (42.2); 2.5682 (0.4); 2.5340 (17.1); 2.5280 (36.5); 2.5220 (50.3); 2.5159 (36.1); 2.5100 (16.8); 2.4556 (0.5); 2.0093 (3.1); 1.2181 (0.9); 1.1944 (1.8); 1.1706 (0.9); 0.0308 (1.3); 0.0199 (43.9); 0.0089 (1.6); −0.0465 (0.4)

TABLE 5 Compounds according to formula (2)

(2) In table 5, ″#″ denotes the point of attachment to the L-R⁶ group. Ex No

L-R⁶ LogP Salt 2-01

3-methylphenyl 3.71^([a]) 2-02

(2,4-dimethylphenyl)methyl 1.60^([a]) TFA 2-03

(2-chloro-4-cyclopropylphenyl)methyl 1.60^([a]) TFA 2-04

(4-cyclopropyl-2-methylphenyl)methyl 1.56^([a]) TFA 2-05

(2,4-dichlorophenyl)methyl 1.54^([a]) TFA 2-06

(2-chloro-4-isopropylphenyl)methyl 1.59^([a]) TFA 2-07

(4-isopropyl-2-methylphenyl)methyl 1.55^([a]) TFA 2-08

(3,4-dimethylphenyl)methyl 1.32[^(a]) TFA 2-09

(4-bromo-2-chlorophenyl)methyl 1.54^([a]) TFA 2-10

(4-bromo-2-methylphenyl)methyl 1.52^([a]) TFA 2-11

(2,4-dichlorophenyl)methyl 4.41^([a]) 2-12

(2,4-dimethylphenoxy)methyl 1.70^([a]) TFA 2-13

(2,4-dimethylphenoxy)methyl 4.51^([a]) 2-14

(4-chlorophenoxy)methyl 1.53^([a]) TFA 2-15

(4-chlorophenoxy)methyl 4.20^([a]) 2-16

[(2,4-dimethylphenyl)thio]methyl 1.79^([a]) TFA 2-17

[(2,4-dimethylphenyl)thio]methyl 4.74^([a]) 2-18

(5-chloropyridin-2-yl)methyl 1.23^([a]) TFA 2-19

(4,5-dimethyl-3-thienyl)methyl 1.64^([a]) TFA 2-20

(2-chloro-4-methylphenyl)methyl 1.61^([a]) TFA 2-21

(2-chloro-4-methylphenyl)methyl 4.51^([a])

TABLE 6 2-01: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 7.8588 (11.8); 7.8355 (0.4); 7.4419 (0.8); 7.4196 (0.8); 7.2178 (0.7); 7.2089 (0.4); 7.1988 (1.9); 7.1804 (1.4); 7.1339 (2.1); 7.1076 (0.8); 7.0372 (1.3); 7.0195 (1.1); 4.7012 (0.5); 4.6852 (0.6); 4.6034 (0.4); 4.1784 (0.5); 4.1695 (0.5); 4.1521 (0.7); 4.1363 (0.3); 4.0846 (0.4); 4.0684 (0.7); 4.0529 (0.5); 4.0431 (0.5); 3.3205 (109.8); 2.6736 (0.3); 2.6694 (0.4); 2.5089 (28.2); 2.5046 (56.6); 2.5001 (75.0); 2.4957 (53.0); 2.4913 (24.6); 2.3317 (0.3); 2.3271 (0.4); 2.3220 (0.3); 2.2878 (11.1); 2.0501 (1.2); 2.0312 (0.4); 2.0151 (0.8); 1.9955 (1.1); 1.9788 (0.9); 1.9636 (0.4); 1.3501 (16.0); 1.2356 (0.6); 1.2103 (0.7); −0.0014 (6.8) 2-02: ¹H-NMR(499.9 MHz, d₆-DMSO): δ = 8.3331 (4.3); 7.8923 (16.0); 7.1867 (2.1); 7.1714 (2.5); 6.9966 (3.3); 6.9726 (2.0); 6.9574 (1.8); 4.2888 (0.8); 4.2756 (1.0); 4.2668 (1.5); 4.2540 (1.5); 4.2169 (1.6); 4.2106 (1.8); 4.1952 (1.1); 4.1888 (1.0); 3.7123 (1.1); 3.7064 (1.1); 3.7009 (1.1); 3.3434 (3.2); 2.9949 (0.4); 2.9828 (0.6); 2.9669 (1.6); 2.9529 (2.4); 2.9328 (1.6); 2.9049 (0.6); 2.5088 (3.2); 2.2745 (12.3); 2.2293 (12.2) 2-03: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.3411 (2.0); 7.8880 (16.0); 7.3658 (2.0); 7.3459 (2.4); 7.1652 (2.8); 7.1612 (2.9); 7.0376 (1.5); 7.0335 (1.5); 7.0178 (1.4); 7.0136 (1.3); 4.2982 (0.4); 4.2822 (0.5); 4.2703 (1.4); 4.2534 (2.0); 4.2407 (1.6); 4.2224 (0.6); 4.2129 (0.4); 3.7788 (0.7); 3.3905 (0.5); 3.3731 (0.4); 3.0783 (2.6); 3.0598 (2.2); 2.5045 (18.0); 2.5002 (23.4); 2.4960 (17.8); 1.9344 (0.6); 1.9259 (0.7); 1.9135 (1.1); 1.9011 (0.7); 1.8927 (0.6); 1.8801 (0.3); 1.1071 (0.3); 1.0895 (0.7); 1.0720 (0.3); 0.9822 (0.6); 0.9711 (2.0); 0.9659 (2.2); 0.9553 (1.3); 0.9503 (2.1); 0.9450 (2.1); 0.9349 (0.9); 0.6997 (0.8); 0.6889 (2.4); 0.6843 (2.4); 0.6768 (2.3); 0.6721 (2.4); 0.6607 (0.8); −0.0017 (2.7) 2-04: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.2662 (1.8); 7.9096 (0.5); 7.8877 (16.0); 7.8654 (0.5); 7.1680 (2.1); 7.1485 (2.3); 6.8848 (2.7); 6.8630 (1.6); 6.8434 (1.4); 4.2706 (0.6); 4.2541 (0.7); 4.2431 (1.4); 4.2270 (1.5); 4.2123 (1.5); 4.2033 (1.6); 4.1851 (0.7); 4.1760 (0.6); 3.6896 (0.7); 3.4075 (0.4); 3.3904 (0.8); 3.3729 (1.0); 3.3554 (0.8); 2.9473 (0.3); 2.9281 (2.4); 2.9128 (1.6); 2.9061 (1.6); 2.5044 (32.8); 2.5000 (43.1); 2.4956 (31.6); 2.3269 (0.3); 2.3139 (0.8); 2.2604 (11.3); 1.8500 (0.6); 1.8416 (0.7); 1.8292 (1.2); 1.8167 (0.8); 1.8083 (0.7); 1.7952 (0.4); 1.1069 (0.4); 1.0894 (0.7); 1.0720 (0.3); 0.9254 (0.8); 0.9148 (2.2); 0.9094 (2.4); 0.9045 (1.2); 0.8994 (1.3); 0.8938 (2.3); 0.8885 (2.3); 0.8786 (0.9); 0.6309 (0.9); 0.6208 (2.4); 0.6159 (2.5); 0.6083 (2.5); 0.6034 (2.4); 0.5926 (0.9); 0.0064 (0.4); −0.0015 (7.0); −0.0099 (0.4) 2-05: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.3427 (3.2); 7.9146 (0.5); 7.8924 (16.0); 7.6434 (3.4); 7.6385 (3.8); 7.5409 (2.2); 7.5202 (3.4); 7.4546 (2.3); 7.4496 (2.3); 7.4340 (1.6); 7.4290 (1.6); 4.2841 (3.5); 4.2717 (4.2); 3.8317 (0.8); 3.8200 (1.2); 3.8061 (0.9); 3.3429 (0.6); 3.1333 (2.4); 3.1288 (2.4); 3.1145 (2.6); 2.5004 (16.3); −0.0018 (4.8) 2-06: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.3621 (1.7); 7.9167 (0.5); 7.9031 (1.8); 7.8934 (13.0); 7.8713 (0.4); 7.8692 (0.4); 7.4399 (2.2); 7.4201 (2.7); 7.3358 (2.9); 7.3317 (3.1); 7.2431 (0.4); 7.2352 (1.7); 7.2310 (1.6); 7.2154 (1.4); 7.2112 (1.3); 4.2830 (1.3); 4.2687 (2.6); 4.2592 (1.8); 4.2414 (0.6); 4.2315 (0.4); 3.8155 (0.6); 3.8062 (0.7); 3.3927 (0.8); 3.3752 (0.8); 3.1039 (2.4); 3.0857 (2.2); 2.9229 (0.4); 2.9057 (0.9); 2.8884 (1.3); 2.8712 (1.0); 2.8540 (0.4); 2.5255 (0.5); 2.5120 (9.0); 2.5076 (18.2); 2.5031 (24.5); 2.4986 (17.4); 2.4942 (8.1); 1.1938 (16.0); 1.1766 (15.6); 1.1551 (0.3); 1.1094 (0.7); 1.0919 (1.4); 1.0744 (0.7); 0.8789 (0.4); 0.0007 (1.9) 2-07: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.3080 (1.3); 7.9160 (0.5); 7.9132 (0.4); 7.9026 (1.6); 7.8938 (11.0); 7.8920 (11.1); 7.8832 (1.6); 7.8699 (0.4); 7.2333 (1.9); 7.2139 (2.3); 7.0596 (2.7); 7.0435 (1.6); 7.0241 (1.3); 4.2877 (0.3); 4.2611 (0.9); 4.2450 (1.0); 4.2321 (1.4); 4.2231 (1.5); 4.2050 (0.6); 4.1959 (0.5); 3.7189 (0.6); 3.3924 (0.6); 3.3749 (0.6); 3.3575 (0.4); 2.9529 (1.8); 2.9342 (1.6); 2.8492 (0.4); 2.8322 (0.9); 2.8149 (1.2); 2.7977 (0.9); 2.7805 (0.4); 2.5112 (11.1); 2.5069 (22.4); 2.5024 (29.8); 2.4979 (21.4); 2.4935 (10.1); 2.3158 (0.4); 2.2934 (11.6); 1.1805 (16.0); 1.1632 (15.6); 1.1091 (0.5); 1.0916 (0.9); 1.0741 (0.4); 0.0006 (2.8) 2-08: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.2269 (1.6); 7.9157 (0.5); 7.9020 (1.9); 7.8923 (16.0); 7.8702 (0.5); 7.1019 (2.0); 7.0847 (5.1); 7.0377 (2.3); 7.0187 (1.3); 5.7587 (0.4); 4.2409 (0.5); 4.2244 (3.6); 4.2137 (2.9); 3.7359 (0.8); 3.7220 (1.0); 3.7096 (0.7); 3.3344 (0.6); 2.9028 (2.6); 2.8853 (2.6); 2.5113 (13.6); 2.5069 (28.1); 2.5024 (38.0); 2.4979 (27.2); 2.4935 (12.8); 2.1946 (15.6); 2.1763 (14.8); 1.1067 (0.9); 0.0007 (3.4) 2-09: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.3668 (3.1); 7.9176 (0.5); 7.8953 (16.0); 7.8726 (0.4); 7.7539 (4.1); 7.7489 (4.3); 7.5803 (1.7); 7.5752 (1.6); 7.5597 (2.5); 7.5547 (2.4); 7.4744 (3.7); 7.4537 (2.5); 4.2906 (2.7); 4.2881 (2.6); 4.2765 (3.8); 4.2592 (0.4); 3.8354 (0.7); 3.8228 (1.0); 3.8088 (0.6); 3.1559 (0.3); 3.1269 (2.0); 3.1205 (2.0); 3.1075 (2.0); 3.1031 (2.0); 2.5126 (6.5); 2.5083 (13.2); 2.5038 (17.8); 2.4994 (12.7); 2.4950 (6.0); 0.0007 (1.2) 2-10: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.3381 (3.4); 7.9140 (0.6); 7.8920 (16.0); 7.8688 (0.6); 7.4251 (2.9); 7.4209 (3.3); 7.3677 (1.4); 7.3630 (1.2); 7.3474 (2.1); 7.3425 (2.0); 7.2808 (3.5); 7.2603 (2.2); 7.1732 (0.4); 4.2842 (0.5); 4.2692 (0.6); 4.2565 (2.0); 4.2429 (3.4); 4.2345 (2.4); 4.2169 (0.7); 4.2067 (0.4); 3.7575 (0.8); 3.7467 (1.0); 3.7332 (0.8); 2.9774 (2.5); 2.9581 (2.9); 2.5060 (6.1); 2.5017 (7.9); 2.4975 (5.8); 2.3132 (15.1); −0.0020 (3.4) 2-11: ¹H-NMR(300.1 MHz, d₆-DMSO): δ = 7.8598 (15.3); 7.5312 (1.4); 7.5249 (1.4); 7.3677 (0.5); 7.3616 (0.4); 7.3400 (1.3); 7.3336 (1.2); 7.3171 (1.6); 7.2894 (0.6); 6.8031 (0.6); 6.7729 (0.6); 4.1931 (0.7); 4.1715 (1.2); 4.1471 (0.6); 3.9005 (0.4); 3.8715 (0.3); 3.3414 (4.6); 2.9636 (0.4); 2.9468 (0.5); 2.9186 (0.6); 2.9025 (0.6); 2.7338 (0.6); 2.7276 (0.6); 2.7037 (0.4); 2.6910 (0.3); 2.5134 (25.8); 2.5074 (51.6); 2.5014 (69.3); 2.4954 (47.3); 2.4895 (21.4); 2.2712 (0.4); 1.9037 (0.5); 1.8769 (0.5); 1.8284 (0.3); 1.2494 (16.0); 1.1197 (1.9); 0.0105 (0.4); −0.0004 (11.5); −0.0115 (0.4) 2-12: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.8522 (0.6); 7.8435 (2.0); 7.8314 (2.3); 7.8278 (2.2); 7.8228 (2.8); 7.8143 (5.7); 7.8030 (3.0); 7.7915 (5.7); 7.7830 (2.6); 7.7738 (2.3); 7.7623 (1.9); 7.3225 (1.3); 7.3170 (0.6); 7.2986 (12.1); 7.2821 (1.1); 7.2740 (3.7); 7.2266 (5.1); 7.2025 (3.0); 7.1728 (0.5); 6.9253 (4.9); 6.9026 (1.8); 6.7442 (2.2); 6.7146 (1.7); 4.7935 (0.5); 4.7654 (0.7); 4.7532 (1.2); 4.7260 (1.2); 4.6923 (1.3); 4.6814 (1.4); 4.6527 (0.7); 4.6413 (0.6); 4.3871 (0.5); 4.3697 (0.6); 4.3529 (1.4); 4.3350 (1.6); 4.3274 (1.6); 4.3096 (1.4); 4.2926 (0.5); 4.2752 (0.5); 4.0616 (0.9); 4.0472 (0.8); 2.3964 (16.0); 2.2962 (1.1); 2.2448 (14.4); 2.2252 (0.7); 2.1836 (14.4); 1.4798 (0.9); 1.4742 (0.8); 1.4532 (0.6); 0.0522 (0.4); 0.0413 (11.8); 0.0307 (0.5) 2-13: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.8812 (1.0); 7.8707 (1.1); 7.8640 (1.0); 7.8617 (0.9); 7.8526 (1.8); 7.8140 (0.3); 7.8010 (1.8); 7.7915 (1.0); 7.7893 (0.9); 7.7826 (1.1); 7.7721 (1.0); 7.2984 (4.6); 6.9715 (1.0); 6.8385 (1.0); 6.8091 (0.7); 5.3378 (4.5); 4.5030 (0.4); 4.4884 (0.4); 4.4521 (0.6); 4.4315 (0.9); 4.4206 (0.5); 4.3968 (0.6); 4.3910 (0.5); 4.1961 (0.5); 4.1788 (0.4); 4.1652 (0.4); 4.1480 (0.3); 2.3504 (0.4); 2.2861 (4.8); 2.2345 (5.0); 1.6061 (2.8); 1.4776 (16.0); 1.4520 (0.4); 0.0378 (6.0) 2-14: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.5726 (0.6); 7.8154 (1.6); 7.8082 (1.3); 7.7999 (3.1); 7.7917 (5.8); 7.7858 (16.0); 7.7776 (15.6); 7.7633 (3.1); 7.7551 (1.2); 7.7479 (1.6); 7.7397 (0.5); 7.3197 (1.1); 7.3142 (0.6); 7.3107 (0.5); 7.2983 (6.6); 7.2793 (1.0); 7.2715 (3.0); 7.2246 (4.2); 7.2040 (10.0); 7.1974 (5.2); 7.1813 (3.2); 7.1742 (10.3); 7.1631 (1.3); 6.8614 (1.1); 6.8502 (9.3); 6.8432 (3.1); 6.8272 (2.7); 6.8202 (7.9); 6.8089 (0.9); 4.7388 (0.9); 4.7115 (1.2); 4.6990 (2.0); 4.6722 (2.2); 4.6450 (2.2); 4.6321 (2.5); 4.6055 (1.2); 4.5925 (1.0); 4.3808 (0.6); 4.3632 (0.9); 4.3462 (2.6); 4.3308 (4.4); 4.3153 (2.9); 4.2983 (0.8); 4.2810 (0.7); 4.0622 (1.2); 4.0486 (1.5); 4.0358 (1.4); 4.0225 (1.0); 2.3937 (12.7); 1.2928 (0.8); 1.2720 (0.8); 0.0406 (5.9) 2-15: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.8812 (0.8); 7.8706 (0.9); 7.8641 (0.7); 7.8615 (0.8); 7.8524 (1.6); 7.8068 (1.6); 7.7975 (0.8); 7.7950 (0.8); 7.7885 (1.0); 7.7779 (0.9); 7.2986 (2.2); 7.2803 (1.6); 7.2729 (0.5); 7.2577 (0.5); 7.2502 (1.9); 6.9369 (1.9); 6.9294 (0.6); 6.9143 (0.5); 6.9068 (1.6); 4.4878 (0.3); 4.4732 (0.4); 4.4138 (0.3); 4.4044 (0.4); 4.3833 (0.6); 4.3490 (0.4); 4.1977 (0.6); 4.1793 (0.4); 4.1667 (0.5); 4.1484 (0.3); 1.6261 (1.1); 1.4799 (16.0); 1.2924 (0.4); 0.0361 (2.8) 2-16: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.8646 (0.6); 7.8551 (0.6); 7.8515 (0.8); 7.8491 (0.7); 7.8431 (1.0); 7.8352 (2.3); 7.8295 (1.2); 7.8227 (1.2); 7.8178 (2.3); 7.8094 (1.0); 7.8035 (0.8); 7.8009 (0.8); 7.7975 (0.6); 7.7879 (0.7); 7.2986 (2.5); 7.2748 (1.2); 6.9980 (1.1); 6.9180 (0.6); 6.8916 (0.5); 4.6936 (0.4); 4.6637 (0.6); 4.6535 (0.6); 4.6026 (0.5); 4.5750 (0.6); 3.7770 (0.3); 3.7694 (16.0); 3.7604 (0.4); 3.4399 (0.4); 3.3922 (0.5); 3.3717 (0.4); 3.1601 (0.5); 3.1326 (0.4); 3.1125 (0.4); 3.0850 (0.3); 2.3843 (5.9); 2.2377 (5.6); 2.2202 (0.9); 0.0376 (2.4) 2-17: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.8888 (1.1); 7.8783 (1.2); 7.8716 (1.1); 7.8693 (1.0); 7.8602 (2.0); 7.8468 (0.4); 7.8241 (0.3); 7.8218 (0.3); 7.8088 (2.0); 7.7993 (1.1); 7.7971 (1.0); 7.7905 (1.2); 7.7799 (1.1); 7.4011 (0.5); 7.3750 (0.6); 7.2982 (3.1); 7.0174 (1.1); 6.9823 (0.5); 4.5948 (0.6); 4.5808 (0.6); 4.5605 (0.7); 4.5466 (0.7); 4.3163 (0.4); 4.3009 (0.4); 4.2822 (0.3); 4.2667 (0.4); 3.2991 (0.6); 3.2742 (0.6); 2.4199 (5.8); 2.2971 (5.6); 1.6199 (2.0); 1.4724 (0.4); 1.4503 (16.0); 1.3035 (1.3); 0.9406 (0.5); 0.9188 (1.5); 0.8957 (0.5); 0.0368 (3.9) 2-19: ¹H-NMR(499.9 MHz, d₆-DMSO): δ = 8.8714 (0.4); 8.2981 (3.5); 7.9160 (0.6); 7.8967 (14.7); 7.8812 (1.2); 7.8789 (1.2); 7.1212 (5.9); 4.2957 (0.4); 4.2810 (4.5); 4.2736 (3.5); 4.2696 (3.4); 4.2471 (0.5); 3.7070 (0.3); 3.6960 (0.9); 3.6858 (1.1); 3.6782 (1.2); 3.6692 (0.9); 3.6585 (0.4); 3.3929 (0.3); 3.3548 (156.6); 2.9562 (0.8); 2.9382 (0.9); 2.9272 (1.6); 2.9093 (1.6); 2.8698 (1.5); 2.8581 (1.7); 2.8409 (1.0); 2.8291 (0.9); 2.5091 (4.1); 2.5061 (5.5); 2.5028 (4.4); 2.2780 (16.0); 2.0370 (15.8); 1.1904 (1.9); 1.1780 (2.0) 2-20: ¹H-NMR(300.2 MHz, d₆-DMSO): δ = 8.3905 (1.6); 7.9068 (16.0); 7.8779 (0.3); 7.4117 (1.8); 7.3858 (2.2); 7.3075 (2.2); 7.1760 (1.2); 7.1728 (1.2); 7.1502 (1.0); 7.1470 (1.0); 5.7761 (0.6); 4.3304 (0.3); 4.3091 (0.4); 4.2933 (1.1); 4.2707 (2.0); 4.2563 (1.4); 4.2320 (0.4); 4.2195 (0.3); 3.8116 (0.5); 3.1178 (2.0); 3.0959 (1.3); 3.0901 (1.3); 2.5342 (1.5); 2.5283 (3.0); 2.5222 (4.1); 2.5162 (3.0); 2.5102 (1.5); 2.2951 (8.9); 1.5526 (4.8); 1.3275 (0.4); 1.1290 (1.1); 0.0169 (3.1) 2-21: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9005 (2.2); 7.8901 (2.5); 7.8833 (2.3); 7.8813 (2.1); 7.8720 (3.8); 7.8585 (0.6); 7.8560 (0.5); 7.8271 (0.6); 7.8245 (0.6); 7.8114 (3.8); 7.8019 (2.4); 7.7931 (2.5); 7.7826 (2.2); 7.3523 (1.4); 7.3265 (1.8); 7.2984 (7.6); 7.2157 (2.3); 7.0894 (1.3); 7.0637 (1.1); 5.3343 (0.4); 4.3680 (0.4); 4.3533 (1.1); 4.3345 (1.5); 4.3215 (0.8); 4.2467 (0.6); 4.2344 (1.1); 4.2115 (1.2); 4.1978 (1.0); 4.1838 (0.6); 4.1707 (0.4); 3.2056 (1.6); 3.1823 (1.5); 2.3394 (10.9); 1.6190 (13.4); 1.3998 (16.0); 0.1059 (0.8); 0.0465 (0.4); 0.0358 (9.5)

TABLE 7 Compounds according to formula (3)

(3) In table 7, ″#″ denotes the point of attachment to the L-R⁶ group and ″*″ denotes the point of attachment to the pyridazin-4-yl group Ex- No R⁷ R⁸ Q

L-R⁶ LogP 3- 02 Cl H 3-(trifluoro- methyl)phenyl

(4-chloro- phenyl)methyl 4.51^([a]); 4.35^([b]) 3- 03 CH₃ H 3-(trifluoro- methyl)phenyl

2,4-dichlorophenyl 4.27^([a]); 4.24^([b]) 3- 04 Cl H 3-(trifluoro- methyl)phenyl

2,4-dichlorophenyl 4.72^([a]); 4.63^([b]) 3- 05 Cl CH₃ 3-(trifluoro- methyl)phenyl

(2,4-dimethyl- phenyl)methyl 4.65^([a]) 3- 06 I H 3-(trifluoro- methyl)phenyl

(2,4-dimethyl- phenyl)methyl 5.03^([a]) 3- 07 CH₃ CH₃ 3-(trifluoro- methyl)phenyl

(2,4-dimethyl- phenyl)methyl 3.99^([a]) 3- 08 CH₃ H 3-cyclopropyl- phenyl

(2,4-dimethyl- phenyl)methyl 4.59^([a]) 3- 09 CH₃ H 3-cyclopropyl- 2-fluorophenyl

(2,4-dimethyl- phenyl)methyl 4.61^([a]) 3- 10 Cl H 3-(trifluoro- methyl)phenyl

(3,4-dimethyl- phenyl)methyl 4.92^([a]) 3- 11 Cl H 3-(trifluoro- methyl)phenyl

(4-bromo-2-chloro- phenyl)methyl 5.16^([a]) 3- 12 Cl H 3-(trifluoro- methyl)phenyl

(4-bromo-2-methyl- phenyl)methyl 5.08^([a]) 3- 13 Cl H 3-(difluoro- methyl)-2- fluorophenyl

(2,4-dimethyl- phenyl)methyl 4.56^([a]) 3- 14 CH₃ H 3-cyclopropyl- 2-fluorophenyl

(4-bromo-2-chloro- phenyl)methyl 4.86^([a]) 3- 15 CH₃ H 3-cyclopropyl- 2-fluorophenyl

(3,4-dimethyl- phenyl)methyl 4.64^([a]) 3- 16 Cl H 3-(trifluoro- methyl)phenyl

(2,4-dimethyl- phenyl)methyl 5.00^([a]) 3- 17 Cl H 3-(trifluoro- methyl)phenyl

(4-cyclopropyl-2- methyl- phenyl)methyl 5.14^([a]) 3- 18 Cl H 3-(trifluoro- methyl)phenyl

(2-chloro-4-cyclo- propyl- phenyl)methyl 5.17^([a]) 3- 19 Cl H 3-(trifluoro- methyl)phenyl

(2-chloro-4- isopropyl- phenyl)methyl 5.48^([a]) 3- 20 CH₃ H 3-(difluoro- methyl)phenyl

(2,4-dimethyl- phenyl)methyl 4.04^([a]) 3- 21 Cl H 3-(trifluoro- methyl)phenyl

(4-isopropyl-2- methyl- phenyl)methyl 5.48^([a]) 3- 22 Cl H 3-(trifluoro- methyl)phenyl

(2,4-dichloro- phenyl)methyl 5.03^([a]) 3- 23 Cl H 5- bromopyridin- 3-yl

(2,4-dimethyl- phenyl)methyl 4.19 & 4.34^([a]) 3- 24 Cl H 6-chloro-5- (trifluoromethyl) pyridin-3-yl

(2,4-dimethyl- phenyl)methyl 5.01^([a]) 3- 25 Cl CH₃ 3-cyclopropyl- 2-fluorophenyl

(4-bromo-2-chloro- phenyl)methyl 5.03^([a]) 3- 26 Cl CH₃ 3-cyclopropyl- 2-fluorophenyl

(2-chloro-4-cyclo- propyl- phenyl)methyl 5.05^([a]) 3- 27 Cl H 3-cyclopropyl- phenyl

(2,4-dimethyl- phenyl)methyl 5.11^([a]) 3- 28 Cl H 3-(1-fluoro- cyclo- propyl)phenyl

(2,4-dimethyl- phenyl)methyl 4.92^([a]) 3- 29 CH₃ H 3-cyclopropyl- 2-fluorophenyl

(2-chloro-4-cyclo- propyl- phenyl)methyl 4.90^([a]) 3- 30 Cl CH₃ 3-cyclopropyl- 2-fluorophenyl

(2,4-dichloro- phenyl)methyl 4.90^([a]) 3- 31 Cl H 3-cyclo- propylphenyl

(2,4-dichloro- phenyl)methyl 5.27^([a]) 3- 32 Cl H 2-fluoro-3- [rac-2,2- difluorocyclo- propyl]phenyl

(2,4-dimethyl- phenyl)methyl 4.85^([a]) 3- 33 CH₃ H 3-(trifluoro- methyl)phenyl

(2,4-dimethyl- phenoxy)methyl 4.56^([a]) 3- 34 CH₃ H 3-(trifluoro- methyl)phenyl

(4-chloro- phenoxy)methyl 4.37^([a]) 3- 35 Cl H 3-(trifluoro- methyl)phenyl

[(2,4-dimethyl- phenyl)thio]methyl 5.28^([a]) 3- 36 Cl CH₃ 2-fluoro-3- [rac-2,2- difluorocyclo- propyl]phenyl

(2,4-dimethyl- phenyl)methyl 4.59^([a]) 3- 37 CH₃ H 2-fluoro-3- (trifluoro- methyl)phenyl

(2,4-dichloro- phenyl)methyl 4.64^([a]) 3- 38 CH₃ H 2-fluoro-3- (trifluoro- methyl)phenyl

(2,4-dimethyl- phenyl)methyl 4.54^([a]) 3- 39 CH₃ H 3-(difluoro- methyl)phenyl

(2,4-dichloro- phenyl)methyl 4.18^([a]) 3- 40 Cl H 2-fluoro-3-(1- fluorocyclo- propyl)phenyl

(2,4-dimethyl- phenyl)methyl 4.97^([a]) 3- 41 Cl CH₃ 2-fluoro-3-(1- fluorocyclo- propyl)phenyl

(2,4-dimethyl- phenyl)methyl 4.62^([a]) 3- 42 CH₃ H 3-chloro-2- fluorophenyl

(2-chloro-4-cyclo- propyl- phenyl)methyl 4.70^([a]) 3- 43 CH₃ H 3-chloro-2- fluorophenyl

(4-cyclopropyl-2- methyl- phenyl)methyl 4.74^([a]) 3- 44 CH₃ H 3-chloro-2- fluorophenyl

(4-bromo-2-methyl- phenyl)methyl 4.62^([a]) 3- 45 CH₃ H 3-chloro-2- fluorophenyl

(3,4-dimethyl- phenyl)methyl 4.42^([a]) 3- 46 CH₃ H 3-(difluoro- methyl)-2- fluorophenyl

(4-cyclopropyl-2- methyl- phenyl)methyl 4.55^([a]) 3- 47 CH₃ H 3-(difluor- omethyl)phenyl

(3,4-dimethyl- phenyl)methyl 4.12^([a]) 3- 48 CH₃ H 3-(difluoro- methyl)phenyl

(4-cyclopropyl-2- methyl- phenyl)methyl 4.37^([a]) 3- 49 CH₃ H 3-(difluoro- methyl)-2- fluorophenyl

(3,4-dimethyl- phenyl)methyl 4.30^([a]) 3- 50 CH₃ H 3-cyclopropyl- 2-fluorophenyl

(4-bromo-2-methyl- phenyl)methyl 4.82^([a]) 3- 51 Cl H 3-(trifluoro- methyl)phenyl

(5-chloropyridin-2- yl)methyl4.15^([a]) 4.06 & 3- 52 Cl H 3-(trifluoro- methyl)phenyl

(4,5-dimethyl-3- thienyl)methyl 4.88^([a]) 3- 53 CH₃ H 3-cyclopropyl- phenyl

(3,4-dimethyl- phenyl)methyl 4.70^([a]) 3- 54 CH₃ H 3-cyclopropyl- phenyl

(4-bromo-2-methyl- phenyl)methyl 4.89^([a]) 3- 55 CH₃ H 3-cyclopropyl- phenyl

(4-cyclopropyl-2- methyl- phenyl)methyl 4.93^([a]) 3- 56 CH₃ H 3-(difluoro- methyl)-2- fluorophenyl

(2-chloro-4-methyl- phenyl)methyl 4.21^([a]) 3- 57 Cl H 3-cyclopropyl- 2-fluorophenyl

(2,4-dimethyl- phenyl)methyl 5.08^([a]) 3- 58 CH₃ H 3-(difluoro- methyl)-2- fluorophenyl

(2,4-dimethyl- phenyl)methyl 4.32^([a])

TABLE 8 3-01: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 9.2013 (1.7); 9.1803 (1.8); 7.8708 (0.7); 7.8670 (0.7); 7.8585 (1.5); 7.8488 (9.6); 7.8452 (9.6); 7.8356 (1.4); 7.8225 (7.4); 7.6798 (0.7); 7.6600 (2.0); 7.6410 (3.5); 7.5973 (2.0); 7.5781 (1.3); 7.5656 (1.5); 7.5462 (1.0); 7.2508 (3.2); 7.2272 (2.0); 7.2060 (1.6); 7.1876 (2.4); 7.1689 (1.0); 7.0456 (1.6); 7.0272 (1.3); 5.3251 (0.4); 5.3114 (0.5); 5.3030 (0.9); 5.2898 (0.8); 5.2812 (0.6); 5.2675 (0.4); 4.3016 (0.3); 4.2851 (0.7); 4.2755 (0.7); 4.2676 (0.6); 4.2593 (1.0); 4.2421 (0.5); 4.1981 (0.5); 4.1838 (1.1); 4.1690 (0.8); 4.1579 (0.7); 4.1428 (0.3); 3.3314 (29.1); 2.6054 (16.0); 2.5118 (9.4); 2.5076 (19.0); 2.5032 (25.5); 2.4987 (18.3); 2.4945 (8.7); 2.2157 (0.3); 2.1967 (0.7); 2.1778 (13.3); 2.1500 (1.0); 2.1357 (0.6); 2.1269 (0.8); 2.1124 (0.5); 2.0773 (5.6); 0.0091 (0.8); 0.0010 (20.0); −0.0072 (0.8) 3-02: ¹H-NMR(400.0 MHz, d₆-DMSO): δ = 8.9386 (2.3); 8.9181 (2.4); 7.9829 (11.3); 7.9103 (0.7); 7.8974 (2.2); 7.8882 (16.0); 7.8857 (15.5); 7.8636 (0.8); 7.8267 (0.4); 7.7634 (0.9); 7.7437 (2.8); 7.7241 (2.8); 7.7078 (3.4); 7.6885 (1.4); 7.6363 (3.9); 7.5592 (2.2); 7.5390 (1.7); 7.3224 (5.6); 7.3015 (6.7); 7.0934 (7.4); 7.0725 (6.2); 6.5891 (0.8); 4.4548 (0.8); 4.4431 (1.0); 4.4342 (1.0); 4.4215 (0.9); 4.4110 (0.6); 4.3400 (1.1); 4.3255 (1.0); 4.3146 (2.4); 4.3009 (1.8); 4.2808 (2.2); 4.2667 (2.0); 4.2555 (1.2); 4.2416 (0.9); 4.0558 (0.7); 4.0380 (2.2); 4.0201 (2.2); 4.0023 (0.8); 3.3237 (121.9); 3.2013 (1.2); 3.1903 (1.3); 3.1660 (1.5); 3.1555 (1.4); 2.8923 (1.4); 2.8681 (1.4); 2.8583 (1.3); 2.8339 (1.1); 2.6707 (1.0); 2.6664 (0.7); 2.5063 (135.6); 2.5019 (175.8); 2.4975 (126.0); 2.3333 (0.8); 2.3287 (1.0); 2.3245 (0.7); 2.0572 (0.6); 2.0367 (0.5); 1.9888 (9.5); 1.3975 (8.3); 1.2410 (0.8); 1.2348 (0.8); 1.2248 (0.5); 1.2123 (0.5); 1.1927 (2.8); 1.1749 (5.4); 1.1570 (2.6); 0.1462 (0.6); 0.0079 (6.0); −0.0003 (140.6); −0.0085 (5.6); −0.1499 (0.6) 3-03: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 9.6166 (1.0); 9.5974 (1.0); 8.3148 (1.3); 7.8731 (16.0); 7.8040 (4.2); 7.7169 (0.4); 7.6979 (1.0); 7.6775 (0.9); 7.6601 (2.4); 7.6548 (2.5); 7.6383 (2.8); 7.6301 (1.8); 7.6220 (0.7); 7.6088 (1.9); 7.5768 (0.9); 7.5582 (0.6); 7.3653 (1.1); 7.3601 (1.1); 7.3443 (1.0); 7.3390 (1.0); 5.7550 (2.5); 5.7371 (0.8); 4.4326 (2.0); 4.4167 (1.9); 4.0379 (0.4); 4.0201 (0.4); 3.3194 (193.5); 2.6794 (1.2); 2.6749 (2.4); 2.6704 (3.2); 2.6659 (2.3); 2.6613 (1.2); 2.6538 (0.4); 2.6330 (9.9); 2.5238 (11.2); 2.5190 (17.7); 2.5105 (183.5); 2.5060 (360.1); 2.5014 (470.6); 2.4968 (346.0); 2.4924 (170.3); 2.3373 (1.0); 2.3328 (2.2); 2.3283 (3.0); 2.3237 (2.1); 2.3193 (1.0); 1.9885 (1.8); 1.1927 (0.5); 1.1749 (1.0); 1.1583 (1.0); −0.0002 (4.2) 3-04: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 9.7249 (0.7); 9.7057 (0.7); 8.1326 (3.5); 7.8726 (12.5); 7.7269 (0.8); 7.7083 (1.5); 7.6806 (0.9); 7.6675 (1.7); 7.6622 (2.0); 7.6500 (1.4); 7.6289 (1.6); 7.4007 (0.8); 7.3954 (0.8); 7.3796 (0.7); 7.3742 (0.7); 5.7426 (0.5); 5.7309 (0.4); 4.4549 (0.9); 4.4481 (0.9); 4.4435 (0.8); 4.4283 (0.7); 3.3216 (34.1); 2.6709 (0.4); 2.5244 (1.3); 2.5196 (2.1); 2.5109 (25.0); 2.5065 (49.9); 2.5019 (65.8); 2.4974 (48.8); 2.4929 (24.4); 2.3780 (0.3); 2.3288 (0.4); 1.9886 (0.4); 1.3978 (16.0); 0.1460 (0.5); 0.0079 (4.4); -0.0002 (106.0); −0.0085 (4.1); −0.1495 (0.5) 3-05: ¹H-NMR(300.2 MHz, d₆-DMSO): δ = 9.1301 (0.8); 9.1012 (0.9); 7.8984 (10.4); 7.7347 (0.9); 7.7088 (1.2); 7.6978 (1.3); 7.6715 (0.4); 7.5699 (1.3); 7.5259 (0.8); 7.5000 (0.6); 7.1130 (1.1); 7.0873 (1.2); 6.8433 (1.3); 6.5679 (0.7); 6.5445 (0.6); 4.5774 (0.3); 4.5625 (0.4); 4.3261 (1.6); 4.3094 (1.2); 3.3512 (16.0); 3.1072 (0.3); 3.0927 (0.4); 3.0589 (0.5); 3.0450 (0.4); 2.8591 (0.4); 2.8254 (0.4); 2.8107 (0.4); 2.5341 (1.4); 2.5282 (3.0); 2.5221 (4.0); 2.5161 (2.9); 2.5101 (1.4); 2.2850 (13.3); 2.0769 (5.5); 0.0193 (3.0) 3-06: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.5193 (1.1); 8.0509 (2.1); 7.8044 (1.6); 7.7976 (1.6); 7.6930 (0.5); 7.6078 (0.9); 7.2987 (3.0); 7.2523 (0.4); 7.2269 (0.5); 7.0071 (0.5); 6.9614 (0.4); 5.3343 (0.4); 3.2164 (0.4); 2.9925 (16.0); 2.9173 (14.6); 2.8370 (4.8); 2.6222 (1.1); 2.4428 (2.4); 2.3666 (0.4); 2.2982 (2.3); 2.2361 (0.3); 1.5414 (0.3); 1.5164 (0.7); 1.4914 (0.8); 0.0327 (3.6) 3-07: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.0489 (2.0); 7.8577 (0.6); 7.8491 (0.5); 7.8433 (1.0); 7.8354 (1.3); 7.8276 (3.8); 7.8167 (3.8); 7.8085 (1.1); 7.8007 (1.0); 7.7944 (0.5); 7.7861 (0.7); 7.6118 (0.6); 7.5848 (0.7); 7.5096 (1.4); 7.4824 (0.8); 7.4580 (1.9); 7.4337 (0.3); 7.4146 (0.6); 7.4070 (0.9); 7.4003 (0.4); 7.3830 (0.4); 7.2985 (8.8); 7.2674 (1.1); 7.2418 (1.3); 7.0242 (1.4); 6.9911 (0.8); 6.9654 (0.7); 4.6662 (0.3); 4.6445 (0.3); 4.6062 (0.9); 4.5956 (0.5); 4.5728 (0.8); 4.5622 (0.6); 4.1676 (0.6); 4.1582 (0.7); 4.1343 (0.6); 4.1249 (0.6); 3.7640 (0.4); 3.7422 (0.5); 3.7201 (0.4); 3.3161 (0.4); 3.2935 (0.4); 3.2700 (0.6); 3.2469 (0.7); 3.2166 (0.8); 3.1920 (0.7); 3.1365 (0.6); 3.1076 (0.6); 3.0907 (0.4); 3.0612 (0.4); 2.9940 (15.4); 2.9172 (13.9); 2.8368 (16.0); 2.6547 (8.3); 2.6132 (2.0); 2.4645 (6.6); 2.3675 (0.7); 2.2977 (11.9); 2.2374 (0.6); 1.6962 (1.0); 1.5315 (0.9); 1.5068 (1.9); 1.4828 (4.4); 1.4618 (3.7); 0.0334 (9.4) 3-08: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.5184 (0.9); 8.4920 (1.0); 8.0672 (5.3); 7.8441 (1.7); 7.8339 (1.8); 7.8276 (1.7); 7.8236 (2.0); 7.8153 (4.1); 7.8009 (1.9); 7.7871 (4.1); 7.7781 (1.9); 7.7741 (1.6); 7.7692 (1.8); 7.7577 (1.7); 7.3651 (1.2); 7.3381 (2.7); 7.3112 (1.8); 7.2985 (10.5); 7.2613 (1.8); 7.2358 (2.1); 7.0980 (0.9); 7.0945 (1.2); 7.0906 (1.2); 7.0872 (1.2); 7.0711 (0.8); 7.0678 (0.9); 7.0634 (1.1); 7.0603 (1.0); 7.0321 (1.9); 7.0273 (2.5); 7.0200 (2.5); 7.0122 (2.2); 7.0072 (1.7); 6.9955 (2.2); 6.9355 (1.2); 6.9095 (1.0); 5.3370 (2.7); 4.6830 (0.4); 4.6704 (0.7); 4.6580 (0.6); 4.6447 (0.7); 4.6327 (0.4); 4.4702 (0.9); 4.4585 (0.8); 4.4382 (1.4); 4.4267 (1.2); 4.3362 (1.3); 4.3236 (1.3); 4.3043 (0.9); 4.2917 (0.8); 3.2161 (2.9); 3.1907 (2.6); 2.9952 (0.9); 2.9231 (0.8); 2.8411 (16.0); 2.7139 (15.1); 2.4400 (10.8); 2.2968 (10.2); 1.9694 (0.6); 1.9581 (0.6); 1.9415 (1.1); 1.9248 (0.6); 1.9135 (0.6); 1.6312 (10.6); 1.0180 (0.4); 1.0001 (1.7); 0.9931 (2.3); 0.9717 (1.7); 0.9652 (2.3); 0.9481 (0.5); 0.7797 (0.7); 0.7697 (1.4); 0.7624 (1.7); 0.7543 (2.1); 0.7470 (1.5); 0.7387 (1.2); 0.7273 (0.4); 0.1073 (0.5); 0.0475 (0.5); 0.0367 (11.2); 0.0258 (0.4) 3-09: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.3935 (0.9); 8.3674 (0.9); 8.0770 (5.2); 7.8323 (1.5); 7.8203 (1.4); 7.8161 (1.4); 7.8115 (1.9); 7.8031 (4.1); 7.7909 (2.2); 7.7791 (4.1); 7.7704 (1.8); 7.7658 (1.5); 7.7615 (1.6); 7.7496 (1.6); 7.2986 (16.3); 7.2715 (1.8); 7.2556 (0.7); 7.2460 (2.1); 7.2284 (1.2); 7.2234 (1.0); 7.2053 (0.9); 7.1997 (0.9); 7.1458 (0.9); 7.1423 (0.8); 7.1193 (1.3); 7.1158 (1.4); 7.0927 (0.6); 7.0892 (0.6); 6.9800 (2.0); 6.9301 (1.1); 6.9049 (0.9); 6.8626 (0.7); 6.8576 (0.7); 6.8360 (1.2); 6.8144 (0.6); 6.8096 (0.5); 5.3380 (1.3); 4.7022 (0.4); 4.6897 (0.7); 4.6769 (0.6); 4.6641 (0.7); 4.6515 (0.4); 4.4842 (0.8); 4.4721 (0.8); 4.4517 (1.4); 4.4397 (1.2); 4.3551 (1.3); 4.3417 (1.2); 4.3227 (0.9); 4.3093 (0.8); 3.2482 (2.8); 3.2231 (2.7); 2.8414 (4.1); 2.7194 (14.8); 2.4454 (10.3); 2.2797 (9.7); 2.1626 (0.4); 2.1518 (0.5); 2.1346 (0.9); 2.1171 (0.5); 2.1064 (0.5); 1.6071 (16.0); 1.0688 (0.4); 1.0567 (1.6); 1.0496 (1.8); 1.0386 (0.8); 1.0349 (0.8); 1.0281 (1.7); 1.0213 (1.6); 1.0093 (0.5); 0.8250 (0.9); 0.8113 (1.6); 0.8077 (1.9); 0.8034 (1.6); 0.7942 (1.7); 0.7912 (1.6); 0.7862 (1.3); 0.7740 (0.6); 0.0477 (0.6); 0.0369 (17.7); 0.0259 (0.7) 3-10: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.3459 (0.6); 8.3201 (0.6); 8.2535 (4.6); 7.8416 (0.7); 7.8331 (0.6); 7.8270 (1.2); 7.8192 (1.4); 7.8112 (4.6); 7.8007 (4.6); 7.7928 (1.3); 7.7849 (1.2); 7.7787 (0.5); 7.7703 (0.7); 7.6720 (1.3); 7.6426 (1.0); 7.6226 (3.0); 7.6197 (2.5); 7.5451 (0.6); 7.5339 (0.8); 7.5269 (0.7); 7.5134 (0.6); 7.2986 (12.7); 7.1382 (1.6); 7.0922 (0.5); 7.0866 (0.4); 7.0668 (1.2); 7.0616 (1.2); 7.0375 (1.9); 7.0120 (0.7); 4.6552 (0.5); 4.6439 (0.4); 4.6320 (0.4); 4.4499 (0.6); 4.4363 (0.6); 4.4170 (1.1); 4.4035 (0.9); 4.3337 (1.0); 4.3212 (1.0); 4.3009 (0.6); 4.2883 (0.6); 4.1961 (0.4); 4.1722 (1.2); 4.1484 (1.2); 4.1247 (0.4); 3.1786 (1.0); 3.1563 (1.8); 3.1301 (0.9); 2.2265 (16.0); 2.0835 (5.2); 1.5879 (9.2); 1.3216 (1.6); 1.2979 (3.3); 1.2740 (1.4); 0.9204 (0.7); 0.1083 (3.2); 0.0491 (0.5); 0.0384 (15.9); 0.0275 (0.6) 3-11: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.4360 (0.7); 8.4091 (0.7); 8.2289 (5.4); 8.2202 (0.5); 7.8510 (0.6); 7.8442 (0.5); 7.8358 (1.2); 7.8277 (2.0); 7.8215 (5.9); 7.8130 (5.7); 7.8070 (2.2); 7.7987 (1.2); 7.7906 (0.4); 7.7837 (0.6); 7.7127 (1.4); 7.6795 (0.4); 7.6542 (1.0); 7.6315 (3.4); 7.6136 (0.4); 7.5532 (0.8); 7.5404 (2.5); 7.5382 (2.6); 7.5232 (0.8); 7.5157 (0.5); 7.3707 (5.5); 7.3657 (3.0); 7.2987 (20.3); 4.8371 (0.4); 4.8240 (0.6); 4.8113 (0.5); 4.7986 (0.6); 4.7868 (0.4); 4.5119 (0.8); 4.4996 (0.8); 4.4786 (1.1); 4.4663 (1.0); 4.3421 (1.0); 4.3306 (1.1); 4.3088 (0.8); 4.2973 (0.8); 4.1720 (0.6); 4.1482 (0.7); 3.4516 (0.6); 3.4246 (0.6); 3.4053 (1.0); 3.3787 (1.0); 3.3038 (1.0); 3.2791 (1.0); 3.2578 (0.6); 3.2332 (0.6); 2.6132 (0.4); 2.5489 (0.4); 2.0833 (2.9); 1.5843 (16.0); 1.3214 (1.0); 1.2977 (2.1); 1.2739 (0.8); 0.9201 (0.7); 0.1078 (1.1); 0.0488 (0.9); 0.0381 (25.5); 0.0272 (0.8) 3-12: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.5824 (0.7); 8.5563 (0.8); 8.2650 (5.2); 7.8456 (0.6); 7.8398 (0.4); 7.8297 (1.0); 7.8163 (6.2); 7.8106 (6.4); 7.7973 (1.1); 7.7806 (0.5); 7.7395 (1.5); 7.6447 (1.2); 7.6215 (3.6); 7.6005 (0.4); 7.5604 (0.9); 7.5517 (1.4); 7.5444 (0.8); 7.5293 (0.8); 7.3595 (2.1); 7.2986 (26.4); 4.6233 (0.5); 4.6048 (0.5); 4.5966 (0.5); 4.4896 (0.9); 4.4791 (0.8); 4.4573 (1.1); 4.4470 (1.1); 4.2482 (1.0); 4.2381 (1.0); 4.2164 (0.8); 4.2059 (0.8); 4.1722 (0.5); 4.1484 (0.5); 3.2868 (0.5); 3.2647 (0.5); 3.2407 (1.0); 3.2189 (1.0); 3.1810 (1.1); 3.1506 (1.1); 3.1352 (0.5); 3.1043 (0.5); 2.5095 (0.5); 2.4966 (1.5); 2.4845 (10.0); 2.0836 (2.1); 1.5811 (16.0); 1.3216 (0.7); 1.2978 (1.6); 1.2741 (0.6); 0.9202 (0.5); 0.1079 (0.9); 0.0489 (1.0); 0.0382 (30.9); 0.0272 (1.2) 3-13: ¹H-NMR(300.2 MHz, d₆-DMSO): δ = 7.9942 (1.7); 7.8900 (3.4); 7.8241 (1.3); 7.3116 (0.5); 7.1359 (0.4); 7.1108 (0.4); 6.8937 (0.5); 4.3518 (0.6); 4.3332 (0.5); 3.3406 (16.0); 2.5340 (0.8); 2.5280 (1.7); 2.5219 (2.4); 2.5158 (1.7); 2.5098 (0.8); 2.3102 (2.1); 2.2774 (0.6); 2.1694 (0.6); 2.1089 (2.0); 0.0201 (2.1) 3-14: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.2952 (0.8); 8.2683 (0.8); 8.0574 (0.3); 8.0321 (4.6); 7.8452 (1.4); 7.8334 (1.4); 7.8290 (1.3); 7.8246 (1.8); 7.8158 (3.8); 7.8037 (2.0); 7.7914 (3.6); 7.7830 (1.7); 7.7784 (1.4); 7.7740 (1.4); 7.7622 (1.4); 7.5135 (2.2); 7.5071 (2.4); 7.3991 (1.4); 7.3718 (2.8); 7.3254 (1.8); 7.3189 (1.7); 7.2990 (17.5); 7.2573 (0.5); 7.2517 (0.5); 7.2301 (1.1); 7.2251 (0.9); 7.2073 (0.9); 7.2014 (0.8); 7.1604 (0.8); 7.1572 (0.8); 7.1340 (1.2); 7.1306 (1.3); 7.1073 (0.6); 7.1040 (0.6); 6.8765 (0.6); 6.8716 (0.6); 6.8500 (1.0); 6.8287 (0.5); 6.8237 (0.5); 5.3373 (1.2); 4.8609 (0.4); 4.8473 (0.6); 4.8347 (0.5); 4.8216 (0.6); 4.8093 (0.4); 4.5003 (0.6); 4.4874 (0.6); 4.4667 (1.3); 4.4541 (1.2); 4.4158 (1.3); 4.4017 (1.3); 4.3822 (0.7); 4.3682 (0.6); 3.3929 (2.7); 3.3677 (2.4); 2.9941 (2.9); 2.9213 (2.5); 2.8413 (12.6); 2.7158 (13.2); 2.7062 (1.4); 2.6599 (0.4); 2.1703 (0.4); 2.1600 (0.4); 2.1427 (0.8); 2.1259 (0.5); 2.1146 (0.4); 1.6004 (16.0); 1.0821 (0.6); 1.0678 (1.3); 1.0607 (1.6); 1.0541 (1.0); 1.0466 (1.0); 1.0391 (1.5); 1.0323 (1.5); 1.0184 (0.8); 0.8339 (0.8); 0.8198 (1.6); 0.8158 (1.7); 0.8127 (1.6); 0.8025 (1.6); 0.7981 (1.7); 0.7813 (0.6); 0.0486 (0.7); 0.0378 (22.2); 0.0268 (0.8) 3-15: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.2283 (0.6); 8.2029 (0.6); 8.0706 (3.3); 8.0561 (0.7); 7.8436 (1.1); 7.8329 (1.2); 7.8269 (1.1); 7.8235 (1.3); 7.8146 (2.5); 7.8015 (0.6); 7.7940 (0.6); 7.7812 (2.5); 7.7722 (1.3); 7.7688 (1.2); 7.7631 (1.3); 7.7521 (1.3); 7.2986 (7.3); 7.2175 (0.3); 7.2119 (0.4); 7.1904 (0.8); 7.1851 (0.7); 7.1681 (0.8); 7.1616 (0.9); 7.1495 (1.6); 7.1146 (1.0); 7.1057 (0.7); 7.0871 (0.6); 7.0800 (0.9); 6.9841 (1.3); 6.9585 (1.0); 6.8660 (0.5); 6.8612 (0.5); 6.8392 (0.8); 6.8189 (0.4); 6.8131 (0.3); 5.3360 (1.4); 4.7020 (0.4); 4.6881 (0.3); 4.6781 (0.4); 4.4263 (0.4); 4.4124 (0.4); 4.3932 (1.1); 4.3794 (1.0); 4.3630 (1.1); 4.3467 (1.0); 4.3298 (0.4); 4.3135 (0.4); 3.2064 (1.5); 3.1830 (1.5); 2.9932 (5.3); 2.9216 (4.5); 2.9204 (4.4); 2.8405 (16.0); 2.7453 (0.7); 2.7189 (9.4); 2.1968 (9.4); 2.1739 (0.7); 2.1525 (0.7); 2.1291 (0.7); 2.1121 (0.4); 2.1006 (0.3); 2.0820 (0.6); 1.6299 (5.6); 1.2962 (0.4); 1.0600 (1.1); 1.0530 (1.2); 1.0425 (0.7); 1.0383 (0.6); 1.0314 (1.1); 1.0248 (1.1); 1.0140 (0.4); 1.0104 (0.4); 0.8251 (0.6); 0.8090 (1.2); 0.8028 (1.1); 0.7930 (1.3); 0.7860 (0.8); 0.7756 (0.4); 0.1072 (2.2); 0.0476 (0.4); 0.0369 (8.9) 3-16: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.5044 (1.3); 8.4786 (1.3); 8.2554 (10.1); 7.8397 (1.0); 7.8320 (0.8); 7.8243 (2.0); 7.8160 (3.4); 7.8101 (10.9); 7.8014 (10.2); 7.7948 (3.0); 7.7866 (2.1); 7.7787 (0.7); 7.7718 (1.0); 7.7066 (2.7); 7.6685 (0.4); 7.6430 (1.8); 7.6206 (6.2); 7.6039 (0.6); 7.5861 (0.3); 7.5687 (1.3); 7.5593 (1.9); 7.5522 (1.3); 7.5449 (0.6); 7.5376 (1.0); 7.5299 (0.6); 7.2982 (12.4); 7.2596 (2.6); 7.2341 (3.0); 7.0138 (3.1); 6.9688 (1.7); 6.9432 (1.4); 4.6767 (0.4); 4.6481 (0.8); 4.6381 (0.7); 4.6256 (0.8); 4.5991 (0.4); 4.5149 (1.5); 4.5033 (1.3); 4.4825 (2.0); 4.4711 (1.7); 4.2888 (1.7); 4.2779 (1.7); 4.2565 (1.4); 4.2456 (1.3); 3.2916 (0.7); 3.2692 (0.7); 3.2458 (1.6); 3.2232 (1.5); 3.1837 (1.6); 3.1546 (1.6); 3.1376 (0.8); 3.1086 (0.7); 2.4490 (16.0); 2.3037 (15.1); 2.0451 (5.9); 1.6237 (1.1); 0.0481 (0.4); 0.0373 (12.0); 0.0264 (0.4) 3-17: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.5172 (1.5); 8.4917 (1.4); 8.2586 (9.3); 8.0646 (0.6); 8.0551 (0.8); 7.8696 (0.4); 7.8382 (1.2); 7.8310 (0.9); 7.8227 (2.2); 7.8144 (3.9); 7.8086 (11.0); 7.8007 (10.7); 7.7867 (2.2); 7.7781 (1.3); 7.7711 (1.1); 7.7196 (2.8); 7.7050 (0.6); 7.6959 (0.5); 7.6857 (0.6); 7.6669 (0.4); 7.6409 (1.8); 7.6185 (6.6); 7.5974 (0.7); 7.5827 (0.4); 7.5646 (1.6); 7.5558 (2.4); 7.5488 (1.6); 7.5415 (0.9); 7.5334 (1.2); 7.5259 (1.0); 7.5201 (0.8); 7.2987 (21.4); 7.2652 (2.8); 7.2392 (3.2); 7.1880 (0.3); 6.9717 (0.4); 6.9096 (3.4); 6.8589 (1.9); 6.8527 (1.9); 6.8329 (1.7); 6.8273 (1.4); 4.6575 (0.4); 4.6279 (0.8); 4.6183 (0.7); 4.6079 (0.8); 4.5797 (0.4); 4.5057 (1.6); 4.4942 (1.4); 4.4734 (2.0); 4.4621 (1.7); 4.4249 (0.4); 4.2767 (1.8); 4.2659 (1.7); 4.2445 (1.5); 4.2337 (1.2); 3.7987 (0.3); 3.7766 (0.9); 3.7543 (1.2); 3.7321 (1.0); 3.7098 (0.4); 3.2814 (0.8); 3.2596 (0.9); 3.2355 (1.7); 3.2213 (1.0); 3.2133 (1.8); 3.1969 (1.8); 3.1717 (3.4); 3.1415 (1.8); 3.1248 (1.0); 3.0951 (0.8); 2.9954 (6.3); 2.9213 (5.5); 2.8406 (5.3); 2.6207 (9.5); 2.4963 (1.1); 2.4786 (0.7); 2.4518 (16.0); 2.4081 (0.4); 2.3767 (0.4); 2.3647 (2.0); 2.0977 (0.3); 1.8906 (0.8); 1.8740 (1.2); 1.8628 (1.3); 1.8461 (2.0); 1.8291 (1.4); 1.8180 (1.2); 1.8011 (0.8); 1.7872 (0.5); 1.7693 (0.4); 1.5298 (2.1); 1.5051 (4.7); 1.4802 (5.1); 0.9920 (1.1); 0.9772 (2.9); 0.9705 (3.2); 0.9564 (1.8); 0.9489 (3.2); 0.9423 (2.9); 0.9285 (1.4); 0.9107 (0.5); 0.9041 (0.5); 0.8822 (0.4); 0.8765 (0.4); 0.7041 (1.4); 0.6896 (3.3); 0.6837 (3.1); 0.6730 (3.1); 0.6676 (3.2); 0.6517 (1.2); 0.6304 (0.4); 0.6126 (0.4); 0.1075 (1.0); 0.0478 (0.8); 0.0370 (26.6); 0.0261 (1.1) 3-18: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.5153 (0.4); 8.3645 (2.0); 8.3380 (2.0); 8.2481 (0.5); 8.2221 (12.5); 8.1835 (0.4); 8.0544 (1.2); 8.0320 (0.6); 7.8893 (0.3); 7.8796 (0.4); 7.8705 (0.6); 7.8413 (2.0); 7.8338 (1.7); 7.8265 (3.8); 7.8183 (5.4); 7.8117 (16.0); 7.8023 (15.4); 7.7958 (4.8); 7.7874 (3.6); 7.7725 (1.8); 7.7630 (0.6); 7.7458 (0.3); 7.7219 (0.7); 7.7113 (0.5); 7.6912 (4.0); 7.6497 (2.9); 7.6280 (9.2); 7.6119 (1.1); 7.5795 (1.0); 7.5622 (2.2); 7.5527 (3.2); 7.5456 (2.3); 7.5305 (1.9); 7.5233 (1.5); 7.5082 (1.0); 7.4973 (0.7); 7.4755 (0.5); 7.4458 (0.4); 7.4342 (0.4); 7.3721 (0.4); 7.3634 (0.4); 7.3538 (0.4); 7.3448 (0.6); 7.3314 (4.6); 7.3046 (6.2); 7.2988 (33.3); 7.2393 (0.5); 7.2295 (0.7); 7.2179 (0.5); 7.2109 (0.6); 7.1984 (0.6); 7.0501 (5.4); 7.0443 (5.6); 7.0276 (0.9); 6.9972 (0.5); 6.9092 (2.9); 6.9033 (2.8); 6.8830 (2.6); 6.8772 (2.5); 4.8343 (0.6); 4.8215 (0.9); 4.8097 (1.4); 4.7972 (1.3); 4.7844 (1.5); 4.7712 (1.0); 4.7589 (0.6); 4.7470 (0.4); 4.5040 (1.9); 4.4907 (1.8); 4.4708 (3.0); 4.4575 (2.7); 4.4039 (0.5); 4.3756 (2.7); 4.3637 (2.8); 4.3423 (1.9); 4.3305 (1.8); 3.7984 (0.6); 3.7764 (1.7); 3.7541 (2.3); 3.7318 (1.8); 3.7096 (0.8); 3.4247 (1.4); 3.3983 (1.3); 3.3785 (2.5); 3.3520 (2.7); 3.3253 (0.3); 3.2891 (2.4); 3.2652 (2.5); 3.2428 (1.5); 3.2174 (2.0); 3.1917 (3.2); 3.1669 (3.3); 3.1421 (1.2); 2.9949 (9.6); 2.9666 (0.6); 2.9204 (8.4); 2.8396 (8.7); 2.6407 (9.4); 2.0914 (0.3); 2.0646 (0.3); 2.0425 (0.5); 1.9762 (0.5); 1.9418 (0.5); 1.9280 (0.5); 1.9139 (0.6); 1.8976 (0.6); 1.8809 (1.0); 1.8645 (1.5); 1.8534 (1.6); 1.8364 (2.6); 1.8197 (1.7); 1.8088 (1.6); 1.7919 (1.1); 1.7652 (0.4); 1.5233 (3.6); 1.4985 (8.6); 1.4737 (10.0); 1.3849 (0.4); 1.2901 (0.5); 1.0269 (1.5); 1.0112 (4.0); 1.0049 (4.5); 0.9899 (2.4); 0.9831 (4.5); 0.9768 (4.3); 0.9621 (2.1); 0.9545 (0.9); 0.9470 (0.8); 0.9322 (0.5); 0.9254 (0.5); 0.9175 (0.5); 0.7240 (0.4); 0.6990 (1.9); 0.6835 (5.0); 0.6781 (4.5); 0.6672 (4.4); 0.6616 (5.2); 0.6455 (1.9); 0.6253 (0.8); 0.6178 (0.6); 0.1064 (1.5); 0.0470 (0.9); 0.0361 (40.4); 0.0254 (2.2) 3-19: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.3834 (1.0); 8.3572 (1.0); 8.2244 (6.6); 8.2184 (1.0); 8.0533 (0.7); 8.0347 (0.4); 7.8415 (1.0); 7.8338 (0.8); 7.8267 (2.0); 7.8186 (2.8); 7.8118 (8.5); 7.8023 (8.3); 7.7958 (2.7); 7.7874 (2.0); 7.7725 (1.0); 7.7187 (0.4); 7.7010 (2.1); 7.6742 (0.5); 7.6484 (1.4); 7.6268 (4.9); 7.6117 (0.7); 7.5862 (0.5); 7.5803 (0.5); 7.5682 (1.3); 7.5593 (1.8); 7.5522 (1.2); 7.5458 (0.8); 7.5372 (1.0); 7.4990 (0.5); 7.3813 (2.2); 7.3551 (2.7); 7.2988 (14.5); 7.2731 (0.4); 7.2231 (2.6); 7.2176 (3.0); 7.1983 (0.5); 7.1925 (0.4); 7.1720 (0.4); 7.1631 (0.4); 7.0740 (1.5); 7.0684 (1.4); 7.0479 (1.3); 7.0421 (1.2); 4.8313 (0.5); 4.8191 (0.8); 4.8063 (0.7); 4.7937 (0.7); 4.7806 (0.5); 4.5133 (1.0); 4.4996 (0.9); 4.4798 (1.5); 4.4662 (1.4); 4.4027 (0.4); 4.3904 (1.4); 4.3786 (1.5); 4.3571 (0.9); 4.3453 (0.9); 3.7957 (0.4); 3.7734 (0.9); 3.7511 (1.2); 3.7289 (0.9); 3.7067 (0.4); 3.4394 (0.8); 3.4129 (0.8); 3.3932 (1.3); 3.3668 (1.3); 3.3043 (1.3); 3.2800 (1.3); 3.2581 (0.8); 3.2337 (0.7); 3.2126 (0.6); 3.1879 (1.7); 3.1631 (1.7); 3.1383 (0.6); 2.9943 (5.7); 2.9193 (5.0); 2.8861 (0.9); 2.8632 (1.2); 2.8394 (6.1); 2.8170 (0.5); 2.6203 (5.5); 1.5190 (1.9); 1.4943 (4.2); 1.4697 (5.3); 1.4517 (4.0); 1.2950 (0.9); 1.2796 (0.7); 1.2721 (1.0); 1.2459 (16.0); 1.2228 (15.7); 1.2064 (1.5); 1.2000 (1.2); 1.1897 (1.0); 1.1832 (1.0); 1.1769 (0.9); 0.9453 (0.4); 0.1066 (0.7); 0.0467 (0.6); 0.0359 (17.5); 0.0250 (0.6) 3-20: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.4697 (0.7); 8.4436 (0.7); 7.9844 (5.3); 7.7663 (1.0); 7.7580 (0.8); 7.7517 (1.8); 7.7439 (2.2); 7.7359 (7.2); 7.7257 (7.0); 7.7180 (2.0); 7.7100 (1.8); 7.7038 (0.8); 7.6954 (1.0); 7.5276 (0.6); 7.5015 (1.8); 7.4751 (1.4); 7.4450 (2.0); 7.3938 (1.6); 7.3695 (2.1); 7.3469 (0.9); 7.3432 (0.8); 7.2979 (3.9); 7.1631 (1.9); 7.1376 (2.2); 6.9112 (2.3); 6.8547 (1.3); 6.8273 (2.2); 6.6395 (2.4); 6.4518 (1.2); 5.2682 (1.3); 4.5955 (0.4); 4.5852 (0.6); 4.5716 (0.6); 4.5593 (0.6); 4.5462 (0.4); 4.4073 (1.0); 4.3950 (0.9); 4.3752 (1.4); 4.3629 (1.3); 4.2464 (1.3); 4.2346 (1.3); 4.2144 (1.0); 4.2026 (0.9); 3.5649 (4.7); 3.3193 (0.7); 3.1593 (0.3); 3.1370 (1.5); 3.1183 (1.8); 3.1149 (1.8); 3.0922 (1.4); 3.0732 (0.3); 2.7622 (1.1); 2.6423 (16.0); 2.3490 (11.7); 2.2027 (11.1); 2.0010 (0.9); 1.2133 (0.5); −0.0536 (3.9) 3-21: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.5383 (1.0); 8.5126 (1.2); 8.2637 (6.8); 8.0688 (0.4); 8.0535 (0.8); 7.8386 (0.8); 7.8321 (0.7); 7.8237 (1.6); 7.8157 (2.6); 7.8095 (8.0); 7.8012 (7.9); 7.7871 (1.7); 7.7802 (1.0); 7.7718 (0.9); 7.7630 (0.4); 7.7298 (2.1); 7.7134 (0.6); 7.7035 (0.4); 7.6953 (0.5); 7.6850 (0.4); 7.6403 (1.4); 7.6178 (4.7); 7.5955 (0.5); 7.5909 (0.5); 7.5723 (1.0); 7.5635 (1.8); 7.5564 (1.2); 7.5412 (1.0); 7.5050 (0.4); 7.3062 (2.1); 7.2988 (12.5); 7.2806 (2.4); 7.0620 (2.5); 7.0464 (0.4); 7.0309 (1.5); 7.0247 (1.4); 7.0050 (1.2); 6.9989 (1.2); 4.6443 (0.6); 4.6339 (0.5); 4.6263 (0.6); 4.6185 (0.6); 4.5212 (1.2); 4.5094 (1.0); 4.4889 (1.5); 4.4772 (1.2); 4.2919 (1.2); 4.2812 (1.2); 4.2596 (1.0); 4.2491 (0.9); 3.7971 (0.3); 3.7748 (0.8); 3.7525 (1.2); 3.7303 (0.9); 3.7080 (0.4); 3.2940 (0.6); 3.2722 (0.6); 3.2479 (1.2); 3.2264 (1.2); 3.2152 (0.7); 3.1902 (1.8); 3.1807 (1.4); 3.1655 (1.8); 3.1509 (1.3); 3.1409 (0.8); 3.1355 (0.7); 3.1048 (0.6); 2.9949 (6.2); 2.9197 (5.3); 2.8876 (1.2); 2.8646 (1.4); 2.8400 (6.3); 2.8190 (0.5); 2.6042 (7.6); 2.4936 (1.1); 2.4803 (11.5); 2.4626 (0.6); 2.4357 (0.4); 2.3897 (1.5); 1.5205 (1.9); 1.4958 (4.2); 1.4712 (5.2); 1.4532 (3.7); 1.2988 (0.8); 1.2859 (0.7); 1.2757 (1.3); 1.2620 (16.0); 1.2390 (15.6); 1.2178 (0.9); 1.2052 (1.2); 1.1983 (1.2); 1.1822 (1.1); 1.1753 (1.1); 0.1075 (0.6); 0.0474 (0.5); 0.0366 (14.6); 0.0257 (0.6) 3-22: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.4361 (0.7); 8.4090 (0.7); 8.2269 (4.4); 7.8510 (0.5); 7.8437 (0.4); 7.8358 (1.1); 7.8276 (1.8); 7.8214 (5.4); 7.8128 (5.3); 7.7983 (1.1); 7.7905 (0.4); 7.7832 (0.5); 7.7082 (1.4); 7.6522 (1.0); 7.6301 (3.2); 7.5558 (0.6); 7.5470 (1.1); 7.5399 (0.7); 7.5244 (0.7); 7.4510 (1.6); 7.4235 (2.0); 7.3909 (1.9); 7.3839 (2.1); 7.2990 (8.4); 7.2317 (1.3); 7.2246 (1.2); 7.2043 (1.0); 7.1972 (0.9); 4.8258 (0.5); 4.8132 (0.5); 4.8002 (0.6); 4.7875 (0.3); 4.5140 (0.7); 4.5016 (0.7); 4.4807 (1.0); 4.4684 (0.9); 4.3435 (1.0); 4.3321 (1.0); 4.3104 (0.7); 4.2989 (0.7); 3.4610 (0.5); 3.4343 (0.5); 3.4151 (0.9); 3.3885 (0.9); 3.3165 (0.9); 3.2920 (0.9); 3.2705 (0.5); 3.2460 (0.5); 1.6008 (16.0); 1.2972 (0.9); 0.9194 (0.7); 0.1080 (2.2); 0.0376 (6.8) 3-23: ¹H-NMR(300.2 MHz, CDCl3): δ = 10.3413 (0.5); 8.7359 (0.5); 8.7298 (0.5); 8.7114 (0.5); 8.7038 (0.5); 8.6767 (3.8); 8.6706 (3.9); 8.6511 (3.8); 8.6433 (3.9); 8.4418 (1.3); 8.4155 (1.3); 8.2757 (0.9); 8.2584 (10.0); 7.9782 (3.0); 7.9711 (4.2); 7.9640 (2.6); 7.8533 (1.5); 7.8446 (1.1); 7.8390 (2.3); 7.8312 (2.9); 7.8228 (8.5); 7.8111 (8.6); 7.8029 (2.9); 7.7951 (2.7); 7.7896 (1.6); 7.7809 (2.5); 7.7694 (0.7); 7.7570 (1.0); 7.7484 (0.5); 7.7391 (0.4); 7.7282 (0.4); 7.2989 (23.3); 7.2605 (2.6); 7.2351 (3.1); 7.0281 (3.1); 6.9991 (1.8); 6.9679 (1.5); 6.9404 (0.6); 6.8727 (0.3); 5.3379 (4.1); 4.6678 (0.3); 4.6383 (0.8); 4.6269 (0.8); 4.6120 (0.8); 4.5897 (0.6); 4.5368 (1.6); 4.5254 (1.3); 4.5042 (1.9); 4.4928 (1.6); 4.2507 (1.7); 4.2403 (1.8); 4.2181 (1.4); 4.2077 (1.3); 3.2966 (0.8); 3.2751 (0.8); 3.2511 (1.7); 3.2290 (1.7); 3.1708 (1.6); 3.1409 (1.5); 3.1251 (0.8); 3.0949 (0.8); 2.4561 (16.0); 2.3220 (15.1); 2.2705 (2.4); 2.2573 (2.8); 1.6017 (12.0); 0.0485 (1.0); 0.0378 (30.5); 0.0268 (1.1) 3-24: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.6979 (1.3); 8.6890 (1.3); 8.4932 (0.6); 8.4672 (0.6); 8.2986 (4.6); 8.2361 (0.6); 8.2166 (0.5); 8.2090 (1.6); 8.1998 (1.6); 7.8517 (0.4); 7.8464 (0.4); 7.8136 (16.0); 7.7975 (0.5); 7.7936 (0.4); 7.7796 (0.3); 7.2988 (12.2); 7.2799 (1.3); 7.2546 (1.5); 7.0399 (2.0); 7.0234 (1.0); 6.9976 (0.7); 5.3381 (1.6); 4.6400 (0.3); 4.6294 (0.4); 4.6128 (0.4); 4.6032 (0.4); 4.5526 (0.8); 4.5414 (0.6); 4.5205 (0.9); 4.5093 (0.7); 4.1878 (0.8); 4.1781 (0.8); 4.1559 (0.7); 4.1461 (0.6); 3.3000 (0.4); 3.2795 (0.4); 3.2542 (0.7); 3.2339 (0.7); 3.1476 (0.8); 3.1160 (0.7); 3.1016 (0.4); 3.0704 (0.4); 2.4713 (8.5); 2.4597 (1.1); 2.3247 (8.2); 1.6005 (1.8); 1.3154 (0.5); 1.2945 (0.6); 0.0487 (0.5); 0.0378 (15.3); 0.0269 (0.5) 3-25: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.8863 (1.7); 7.8756 (2.0); 7.8698 (1.8); 7.8660 (2.2); 7.8573 (4.5); 7.8425 (1.8); 7.8281 (4.4); 7.8191 (2.2); 7.8158 (1.9); 7.8100 (2.0); 7.7989 (1.8); 7.4866 (2.8); 7.4801 (3.0); 7.3678 (2.1); 7.3403 (4.1); 7.3100 (1.5); 7.2989 (18.0); 7.2463 (1.9); 7.2398 (1.8); 7.2190 (1.3); 7.2125 (1.2); 7.0709 (3.0); 7.0588 (1.8); 7.0557 (1.9); 7.0511 (1.9); 7.0460 (3.1); 7.0242 (0.4); 6.8095 (0.7); 6.7968 (0.6); 6.7884 (1.1); 6.7773 (1.2); 6.7660 (0.6); 6.7555 (0.6); 5.3380 (1.8); 4.8528 (0.5); 4.8445 (0.6); 4.8250 (0.6); 4.6138 (1.1); 4.6002 (1.0); 4.5789 (1.4); 4.5656 (1.2); 4.3315 (1.3); 4.3200 (1.3); 4.2968 (1.1); 4.2853 (1.0); 3.4323 (0.7); 3.4025 (0.7); 3.3853 (1.2); 3.3557 (1.2); 3.2941 (1.2); 3.2729 (1.2); 3.2474 (0.7); 3.2264 (0.6); 2.8395 (1.1); 2.4032 (16.0); 2.3576 (1.1); 2.0614 (0.5); 2.0505 (0.6); 2.0332 (1.1); 2.0161 (0.6); 2.0050 (0.6); 1.6025 (15.2); 1.2916 (0.4); 1.0292 (0.7); 1.0150 (1.6); 1.0077 (1.9); 0.9935 (1.2); 0.9863 (1.7); 0.9793 (1.9); 0.9653 (0.9); 0.7820 (0.9); 0.7674 (2.1); 0.7625 (2.2); 0.7503 (2.1); 0.7448 (2.4); 0.7289 (0.8); 0.1073 (7.5); 0.0482 (0.8); 0.0375 (22.5); 0.0266 (0.9) 3-26: ¹H-NMR(300.2 MHz, d₆-DMSO): δ = 7.9029 (1.6); 7.1243 (0.4); 7.1184 (0.5); 3.3492 (16.0); 2.5345 (0.8); 2.5287 (1.7); 2.5227 (2.4); 2.5167 (1.7); 2.5109 (0.8); 2.2965 (1.6); 0.0206 (1.6) 3-27: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.4821 (0.4); 8.4555 (0.4); 8.2039 (2.9); 8.0482 (1.8); 7.8413 (0.7); 7.8316 (0.6); 7.8280 (0.8); 7.8257 (0.8); 7.8201 (1.0); 7.8117 (2.3); 7.8051 (1.1); 7.7992 (1.3); 7.7927 (2.2); 7.7845 (1.1); 7.7791 (0.8); 7.7759 (0.8); 7.7721 (0.9); 7.7629 (1.0); 7.7533 (0.4); 7.3814 (0.5); 7.3554 (1.1); 7.3292 (0.7); 7.2988 (3.2); 7.2373 (0.8); 7.2118 (1.0); 7.0975 (0.5); 7.0926 (0.5); 7.0897 (0.6); 7.0695 (0.7); 7.0632 (1.1); 7.0384 (0.7); 7.0229 (0.9); 7.0164 (1.1); 7.0102 (0.6); 6.9931 (1.1); 6.9646 (0.3); 6.9334 (0.6); 6.9091 (0.6); 4.6506 (0.4); 4.6237 (0.4); 4.4819 (0.4); 4.4702 (0.4); 4.4496 (0.6); 4.4379 (0.6); 4.3193 (0.6); 4.3075 (0.6); 4.2871 (0.5); 4.2753 (0.4); 3.2222 (0.4); 3.2058 (1.0); 3.1988 (1.1); 3.1820 (1.0); 3.1723 (1.0); 2.9944 (14.4); 2.9134 (16.0); 2.8347 (11.5); 2.4264 (5.0); 2.3482 (1.2); 2.3261 (0.4); 2.2939 (4.7); 2.2345 (1.1); 1.9470 (0.5); 1.5072 (1.0); 1.4820 (4.7); 1.4584 (3.9); 1.4479 (3.3); 1.4257 (3.0); 1.0156 (0.7); 1.0083 (1.1); 0.9870 (0.8); 0.9808 (1.1); 0.7684 (0.7); 0.7601 (0.6); 0.7519 (1.1); 0.7462 (0.6); 0.7425 (0.6); 0.7360 (0.6); 0.0317 (3.6) 3-28: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.4990 (0.5); 8.4731 (0.5); 8.2278 (3.6); 7.8700 (0.4); 7.8442 (0.8); 7.8319 (1.0); 7.8230 (1.2); 7.8148 (2.8); 7.8079 (1.3); 7.8031 (1.2); 7.7960 (2.7); 7.7877 (1.1); 7.7822 (0.8); 7.7792 (0.9); 7.7665 (0.8); 7.5092 (0.4); 7.4830 (1.1); 7.4567 (1.2); 7.2989 (16.2); 7.2561 (1.0); 7.2490 (1.6); 7.2237 (1.7); 7.1938 (1.0); 7.1660 (0.8); 7.0652 (0.4); 7.0057 (1.3); 6.9536 (0.7); 6.9277 (0.6); 4.6582 (0.4); 4.6322 (0.4); 4.4994 (0.6); 4.4877 (0.5); 4.4669 (0.8); 4.4554 (0.7); 4.3172 (0.7); 4.3057 (0.7); 4.2850 (0.6); 4.2734 (0.5); 4.1726 (0.4); 4.1488 (0.4); 3.2266 (0.8); 3.2038 (1.4); 3.1764 (0.8); 2.4747 (1.0); 2.4394 (6.4); 2.3484 (0.9); 2.3013 (6.0); 2.0840 (1.8); 1.5876 (16.0); 1.5705 (0.9); 1.5638 (1.0); 1.5440 (0.4); 1.5266 (0.4); 1.5073 (0.8); 1.5001 (1.0); 1.4801 (0.4); 1.3221 (0.6); 1.2983 (1.5); 1.2745 (0.5); 1.1723 (0.5); 1.1674 (1.0); 1.1602 (1.0); 1.1432 (0.6); 1.1378 (1.2); 1.1302 (0.9); 0.9207 (0.8); 0.0495 (0.7); 0.0387 (19.3); 0.0277 (0.7) 3-29: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.2631 (1.1); 8.2369 (1.1); 8.0329 (5.4); 7.8263 (1.7); 7.8151 (2.0); 7.8100 (1.9); 7.8060 (2.2); 7.7970 (4.5); 7.7834 (2.3); 7.7698 (4.5); 7.7613 (2.1); 7.7575 (2.0); 7.7518 (2.0); 7.7409 (1.7); 7.3521 (2.3); 7.3258 (2.6); 7.2992 (2.2); 7.2505 (0.6); 7.2453 (0.7); 7.2231 (1.4); 7.2006 (1.0); 7.1951 (1.0); 7.1454 (1.1); 7.1187 (1.8); 7.0919 (0.9); 7.0364 (2.6); 7.0307 (2.8); 6.8586 (2.2); 6.8524 (1.7); 6.8378 (1.7); 6.8326 (2.1); 6.8262 (1.5); 6.8174 (0.8); 6.8122 (0.7); 5.3275 (0.9); 4.8378 (0.5); 4.8247 (0.8); 4.8118 (0.7); 4.7991 (0.8); 4.7858 (0.5); 4.4842 (0.5); 4.4706 (0.5); 4.4509 (1.8); 4.4340 (2.5); 4.4190 (1.8); 4.3997 (0.6); 4.3855 (0.5); 3.3667 (3.3); 3.3421 (3.2); 2.8345 (6.3); 2.6990 (16.0); 2.6037 (0.4); 2.1628 (0.5); 2.1518 (0.6); 2.1347 (1.0); 2.1237 (0.5); 2.1174 (0.6); 2.1067 (0.6); 2.0755 (0.5); 1.8449 (0.6); 1.8335 (0.6); 1.8170 (1.2); 1.8003 (0.7); 1.7891 (0.7); 1.7718 (0.4); 1.7563 (4.3); 1.2901 (0.4); 1.0714 (0.6); 1.0560 (2.0); 1.0496 (2.1); 1.0354 (1.3); 1.0278 (2.1); 1.0212 (2.1); 1.0074 (1.0); 0.9964 (0.9); 0.9804 (2.1); 0.9742 (2.2); 0.9589 (1.2); 0.9524 (2.2); 0.9461 (2.0); 0.9315 (1.0); 0.8273 (0.9); 0.8089 (2.4); 0.7958 (2.2); 0.7906 (2.4); 0.7743 (0.8); 0.6810 (0.9); 0.6651 (2.6); 0.6599 (2.3); 0.6492 (2.2); 0.6432 (2.7); 0.6272 (0.8); 0.0330 (1.0) 3-30: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.8866 (0.9); 7.8755 (0.9); 7.8701 (0.8); 7.8663 (1.0); 7.8575 (2.1); 7.8425 (0.7); 7.8277 (2.1); 7.8189 (1.0); 7.8152 (0.9); 7.8098 (0.9); 7.7985 (0.9); 7.4293 (1.1); 7.4017 (1.4); 7.3361 (1.7); 7.3289 (1.6); 7.3121 (0.6); 7.2988 (11.9); 7.1049 (0.8); 7.0978 (0.8); 7.0775 (0.8); 7.0688 (1.8); 7.0577 (0.9); 7.0547 (0.8); 7.0433 (1.6); 6.8091 (0.3); 6.7877 (0.6); 6.7765 (0.5); 4.6153 (0.5); 4.6019 (0.5); 4.5807 (0.7); 4.5674 (0.6); 4.3340 (0.6); 4.3224 (0.6); 4.2994 (0.5); 4.2878 (0.5); 3.4448 (0.3); 3.3979 (0.6); 3.3686 (0.6); 3.3091 (0.6); 3.2879 (0.6); 3.2621 (0.3); 2.4047 (8.1); 2.0826 (0.8); 2.0313 (0.5); 1.5965 (16.0); 1.3209 (0.4); 1.2972 (0.8); 1.0284 (0.4); 1.0143 (0.8); 1.0069 (0.9); 0.9927 (0.5); 0.9855 (0.8); 0.9785 (0.9); 0.9645 (0.4); 0.9199 (0.5); 0.7805 (0.4); 0.7659 (1.0); 0.7598 (1.0); 0.7488 (0.9); 0.7429 (1.0); 0.7273 (0.4); 0.1075 (0.7); 0.0488 (0.4); 0.0379 (13.7); 0.0270 (0.5) 3-31: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.3987 (0.7); 8.3709 (0.7); 8.1721 (3.4); 8.0509 (2.0); 7.8531 (0.8); 7.8435 (0.7); 7.8402 (0.9); 7.8374 (1.0); 7.8318 (1.3); 7.8235 (2.6); 7.8170 (1.4); 7.8116 (1.3); 7.8051 (2.6); 7.7970 (1.1); 7.7913 (0.9); 7.7884 (0.9); 7.7755 (0.8); 7.4219 (1.3); 7.4110 (0.4); 7.3947 (2.1); 7.3831 (0.4); 7.3710 (2.1); 7.3649 (2.0); 7.3426 (0.8); 7.2988 (5.7); 7.1704 (1.0); 7.1633 (0.9); 7.1431 (0.8); 7.1360 (0.7); 7.0860 (0.8); 7.0786 (1.4); 7.0586 (0.6); 7.0507 (1.3); 7.0106 (1.0); 7.0042 (1.3); 6.9977 (0.7); 4.8128 (0.3); 4.8010 (0.3); 4.7890 (0.4); 4.4865 (0.4); 4.4743 (0.5); 4.4531 (0.8); 4.4410 (0.7); 4.3817 (0.8); 4.3691 (0.8); 4.3485 (0.5); 4.3359 (0.4); 3.7742 (0.4); 3.7605 (0.4); 3.7520 (0.6); 3.7384 (0.6); 3.7300 (0.5); 3.7162 (0.4); 3.3757 (0.8); 3.3465 (1.2); 3.3215 (0.7); 3.2256 (0.8); 3.2113 (0.8); 3.2010 (0.8); 3.1865 (0.8); 3.1763 (0.3); 2.9972 (16.0); 2.9679 (1.3); 2.9160 (13.5); 2.8344 (13.6); 2.0459 (0.4); 1.9732 (0.3); 1.9564 (0.6); 1.9396 (0.4); 1.9286 (0.3); 1.5261 (1.7); 1.4985 (7.0); 1.4759 (7.3); 1.4637 (6.3); 1.4415 (6.0); 1.0278 (0.9); 1.0207 (1.2); 0.9992 (0.9); 0.9930 (1.2); 0.9757 (0.3); 0.7739 (0.8); 0.7676 (1.0); 0.7598 (1.0); 0.7575 (1.0); 0.7508 (0.9); 0.7437 (0.7); 0.1032 (0.4); 0.0322 (6.1) 3-32: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.3902 (0.3); 8.3776 (0.4); 8.2485 (2.0); 8.2445 (1.9); 7.8314 (0.3); 7.8249 (0.4); 7.8170 (0.6); 7.8093 (0.9); 7.8021 (2.0); 7.7950 (2.1); 7.7903 (2.1); 7.7857 (2.0); 7.7703 (0.6); 7.7595 (0.3); 7.3966 (0.3); 7.3148 (0.3); 7.3103 (0.6); 7.2983 (47.4); 7.2862 (0.5); 7.2716 (0.6); 7.2609 (0.9); 7.2466 (0.6); 7.2339 (1.3); 7.2055 (0.6); 7.1788 (0.4); 7.1580 (0.5); 6.9986 (1.0); 6.9475 (0.6); 6.9274 (0.4); 4.5010 (0.4); 4.4783 (0.4); 4.4678 (0.5); 4.4585 (0.3); 4.3120 (0.6); 4.3003 (0.4); 4.2795 (0.4); 3.2424 (0.4); 3.2248 (0.9); 3.1982 (0.5); 2.8969 (0.3); 2.4529 (2.9); 2.4436 (2.9); 2.2904 (3.9); 1.9406 (0.4); 1.7484 (0.4); 1.7340 (0.3); 1.7208 (0.4); 1.7062 (0.3); 1.5764 (16.0); 0.0486 (2.1); 0.0470 (1.3); 0.0378 (65.6); 0.0301 (2.3); 0.0286 (2.2); 0.0270 (2.6); 0.0199 (0.5); 0.0169 (0.4) 3-33: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.5695 (0.9); 8.5428 (0.9); 8.1512 (5.4); 7.8535 (1.6); 7.8437 (1.4); 7.8412 (1.7); 7.8373 (1.7); 7.8325 (2.2); 7.8239 (4.4); 7.8142 (2.1); 7.8123 (2.0); 7.8026 (4.3); 7.7939 (1.9); 7.7891 (1.6); 7.7852 (1.6); 7.7829 (1.3); 7.7730 (1.7); 7.6511 (1.7); 7.6487 (1.8); 7.5778 (2.8); 7.5602 (3.9); 7.5149 (0.3); 7.5031 (0.9); 7.4951 (0.9); 7.4864 (1.0); 7.4805 (1.0); 7.4726 (0.5); 7.4640 (0.4); 7.2987 (14.7); 6.9608 (0.8); 6.9335 (1.2); 6.9084 (1.9); 6.8146 (2.2); 6.7873 (1.6); 4.9746 (0.4); 4.9615 (0.5); 4.9564 (0.6); 4.9450 (0.6); 4.9350 (0.5); 4.9294 (0.5); 4.9171 (0.4); 4.6717 (0.7); 4.6535 (0.7); 4.6372 (1.6); 4.6191 (1.4); 4.5929 (1.5); 4.5742 (1.5); 4.5586 (0.8); 4.5397 (0.7); 4.5071 (0.9); 4.4947 (0.9); 4.4748 (1.2); 4.4625 (1.1); 4.3257 (1.2); 4.3079 (1.1); 4.2932 (0.9); 4.2756 (0.8); 2.7625 (16.0); 2.3243 (0.7); 2.2625 (10.2); 2.2419 (0.8); 2.0839 (1.1); 2.0382 (10.5); 2.0223 (0.9); 1.6177 (0.5); 1.2977 (0.6); 0.1083 (0.7); 0.0488 (0.7); 0.0380 (18.0); 0.0289 (0.5); 0.0271 (0.7) 3-34: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.5428 (1.0); 8.5272 (1.0); 8.0976 (5.5); 7.8042 (1.8); 7.7977 (2.1); 7.7941 (1.8); 7.7923 (2.2); 7.7867 (4.2); 7.7784 (0.9); 7.7727 (0.9); 7.7647 (4.1); 7.7594 (2.0); 7.7577 (1.9); 7.7538 (2.1); 7.7475 (1.9); 7.6265 (1.9); 7.5520 (1.9); 7.5489 (1.5); 7.5434 (3.7); 7.5418 (4.3); 7.4779 (0.8); 7.4730 (0.8); 7.4702 (1.0); 7.4664 (1.1); 7.4600 (0.7); 7.4548 (0.5); 7.2610 (6.7); 7.1930 (0.4); 7.1860 (4.1); 7.1817 (1.4); 7.1724 (1.3); 7.1680 (4.7); 7.1612 (0.5); 6.8142 (0.4); 6.8073 (4.5); 6.8029 (1.5); 6.7937 (1.3); 6.7893 (4.2); 6.7824 (0.4); 5.2976 (12.8); 4.8559 (0.4); 4.8477 (0.5); 4.8446 (0.6); 4.8377 (0.6); 4.8329 (0.6); 4.8297 (0.6); 4.8216 (0.4); 4.6262 (1.1); 4.6160 (1.0); 4.6054 (1.4); 4.5952 (1.3); 4.5027 (1.1); 4.4948 (1.2); 4.4910 (1.5); 4.4833 (1.5); 4.4796 (1.7); 4.4758 (1.4); 4.4701 (1.2); 4.4588 (1.0); 4.2768 (1.2); 4.2651 (1.2); 4.2575 (1.1); 4.2459 (1.0); 4.1279 (0.5); 4.1136 (0.5); 2.7296 (16.0); 2.0432 (2.2); 1.5759 (3.8); 1.2726 (0.6); 1.2583 (1.2); 1.2440 (0.6); −0.0002 (8.6); −0.0067 (0.4) 3-35: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.5282 (1.4); 8.5031 (1.4); 8.2283 (9.2); 7.8325 (0.5); 7.8299 (0.5); 7.8120 (1.7); 7.8004 (13.8); 7.7984 (13.2); 7.7868 (1.6); 7.7687 (0.5); 7.6989 (2.7); 7.6205 (1.6); 7.6000 (6.2); 7.5858 (0.7); 7.5782 (0.8); 7.5716 (0.5); 7.5619 (1.4); 7.5511 (1.6); 7.5443 (1.3); 7.5305 (0.9); 7.5230 (0.6); 7.4021 (2.7); 7.3760 (3.1); 7.2983 (3.6); 6.9851 (3.1); 6.9668 (1.8); 6.9404 (1.4); 4.7335 (1.3); 4.7178 (1.5); 4.6995 (1.5); 4.6838 (1.9); 4.5878 (0.6); 4.5756 (0.8); 4.5637 (0.8); 4.5540 (0.8); 4.5434 (0.6); 4.4162 (1.7); 4.4036 (1.6); 4.3822 (1.5); 4.3697 (1.3); 3.5093 (1.0); 3.4891 (1.0); 3.4626 (1.9); 3.4426 (1.7); 3.3731 (1.8); 3.3489 (1.8); 3.3264 (1.0); 3.3022 (1.0); 2.3679 (16.0); 2.2643 (15.3); 2.0399 (4.0); 0.0372 (4.3) 3-36: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.2432 (0.3); 7.8764 (1.4); 7.8694 (1.7); 7.8655 (1.9); 7.8598 (2.3); 7.8562 (2.4); 7.8480 (4.3); 7.8406 (3.9); 7.8340 (2.4); 7.8286 (2.3); 7.8211 (4.0); 7.8165 (4.4); 7.8081 (2.7); 7.8030 (3.0); 7.7920 (2.0); 7.7872 (1.8); 7.7735 (0.6); 7.7002 (0.4); 7.6352 (0.8); 7.6082 (0.8); 7.5411 (0.8); 7.5138 (0.9); 7.2986 (26.5); 7.2825 (0.4); 7.2708 (0.6); 7.2574 (2.4); 7.2490 (2.0); 7.2317 (3.1); 7.2245 (2.2); 7.2135 (1.3); 7.2067 (0.9); 7.1492 (1.2); 7.1228 (2.5); 7.0961 (1.5); 7.0625 (1.2); 7.0402 (1.5); 7.0130 (2.3); 6.9953 (1.8); 6.9755 (1.3); 6.9494 (2.0); 6.9247 (0.8); 4.7062 (0.5); 4.6947 (0.7); 4.6794 (0.8); 4.6671 (0.9); 4.6547 (0.8); 4.6423 (0.6); 4.6287 (1.2); 4.6183 (0.8); 4.6081 (1.0); 4.5957 (1.6); 4.5842 (0.9); 4.5742 (1.0); 4.5632 (0.8); 4.2118 (0.9); 4.2015 (1.0); 4.1921 (0.9); 4.1807 (1.2); 4.1679 (0.9); 4.1575 (1.0); 4.1478 (0.8); 3.3161 (0.5); 3.3021 (0.6); 3.2937 (0.6); 3.2702 (1.0); 3.2557 (1.0); 3.2474 (1.0); 3.2328 (0.8); 3.1625 (1.4); 3.1346 (1.4); 3.1172 (0.8); 3.0879 (0.7); 2.8309 (0.5); 2.8038 (0.6); 2.7912 (1.0); 2.7633 (1.0); 2.7510 (0.6); 2.7229 (0.6); 2.6022 (4.0); 2.5343 (3.7); 2.4856 (1.3); 2.4605 (9.3); 2.4514 (9.3); 2.4195 (11.8); 2.4046 (12.6); 2.3737 (1.4); 2.3543 (1.2); 2.3160 (1.3); 2.2880 (9.0); 2.2646 (7.7); 2.2397 (1.4); 2.0834 (0.7); 1.9456 (0.4); 1.9282 (0.4); 1.9191 (0.5); 1.9018 (0.9); 1.8886 (0.6); 1.8849 (0.6); 1.8789 (0.8); 1.8752 (0.7); 1.8619 (0.9); 1.8491 (0.3); 1.8449 (0.3); 1.8398 (0.4); 1.8189 (0.4); 1.6966 (0.4); 1.6855 (0.5); 1.6692 (0.7); 1.6569 (1.1); 1.6440 (0.7); 1.6298 (1.0); 1.6144 (0.9); 1.6008 (16.0); 1.2975 (0.6); 0.0489 (1.1); 0.0379 (33.4); 0.0271 (1.2) 3-37: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.3020 (0.4); 8.2763 (0.4); 8.0712 (2.2); 8.0521 (1.0); 7.8195 (0.6); 7.8114 (0.8); 7.8047 (2.9); 7.7954 (2.9); 7.7891 (0.9); 7.7807 (0.6); 7.7656 (0.3); 7.6933 (0.5); 7.5960 (0.4); 7.4730 (0.9); 7.4455 (1.1); 7.4034 (0.4); 7.3777 (1.5); 7.3709 (1.4); 7.2989 (16.2); 7.2324 (0.7); 7.2255 (0.6); 7.2052 (0.5); 7.1980 (0.5); 4.5166 (0.4); 4.5040 (0.4); 4.4833 (0.6); 4.4707 (0.5); 4.3607 (0.5); 4.3480 (0.5); 4.3279 (0.4); 4.3150 (0.4); 3.4103 (0.6); 3.3830 (0.6); 3.3698 (0.5); 3.3460 (0.6); 2.9942 (8.6); 2.9204 (7.4); 2.8400 (1.0); 2.7548 (0.8); 2.7398 (6.2); 1.6330 (16.0); 1.5291 (0.4); 0.1059 (1.9); 0.0470 (0.6); 0.0362 (19.9); 0.0253 (0.8) 3-38: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.3877 (0.9); 8.3621 (0.9); 8.1146 (5.5); 7.8174 (0.6); 7.8107 (0.5); 7.8020 (1.3); 7.7940 (2.4); 7.7880 (7.4); 7.7802 (7.3); 7.7745 (2.3); 7.7662 (1.3); 7.7576 (0.4); 7.7504 (0.6); 7.7189 (0.6); 7.6955 (1.2); 7.6726 (0.7); 7.6687 (0.7); 7.6099 (0.6); 7.5876 (1.1); 7.5662 (0.7); 7.3902 (0.8); 7.3638 (1.3); 7.3358 (0.6); 7.2985 (11.9); 7.2876 (2.0); 7.2618 (2.1); 6.9997 (2.2); 6.9661 (1.2); 6.9403 (1.0); 5.3372 (0.7); 4.6667 (0.6); 4.6560 (0.5); 4.6453 (0.6); 4.5108 (1.1); 4.4988 (0.9); 4.4785 (1.4); 4.4667 (1.2); 4.3054 (1.2); 4.2936 (1.2); 4.2733 (1.0); 4.2614 (0.9); 3.3085 (0.4); 3.2865 (0.4); 3.2625 (1.2); 3.2404 (1.2); 3.2220 (1.3); 3.1934 (1.2); 3.1759 (0.5); 3.1473 (0.4); 2.7440 (16.0); 2.4622 (11.3); 2.2860 (10.7); 1.5950 (5.1); 0.1086 (0.4); 0.0492 (0.5); 0.0383 (15.0); 0.0275 (0.6) 3-39: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.4206 (0.9); 8.3936 (0.9); 8.0605 (5.6); 7.8468 (1.4); 7.8373 (1.2); 7.8339 (1.6); 7.8312 (1.6); 7.8255 (2.1); 7.8171 (4.7); 7.8112 (2.2); 7.8052 (2.0); 7.7990 (4.8); 7.7908 (1.9); 7.7851 (1.8); 7.7823 (1.7); 7.7789 (1.3); 7.7693 (1.5); 7.6107 (0.6); 7.5846 (1.6); 7.5581 (1.4); 7.5378 (1.8); 7.4785 (1.5); 7.4546 (4.1); 7.4273 (3.5); 7.3741 (2.8); 7.3671 (3.1); 7.2988 (15.5); 7.2021 (1.7); 7.1950 (1.7); 7.1748 (1.5); 7.1676 (1.4); 7.1028 (0.4); 7.0964 (0.4); 6.9043 (1.1); 6.7163 (2.3); 6.5285 (1.2); 4.8523 (0.4); 4.8402 (0.7); 4.8280 (0.6); 4.8154 (0.7); 4.8030 (0.4); 4.4895 (0.9); 4.4771 (0.8); 4.4564 (1.5); 4.4441 (1.4); 4.3807 (1.5); 4.3684 (1.5); 4.3478 (0.9); 4.3353 (0.8); 3.4499 (0.5); 3.4229 (0.5); 3.4038 (1.3); 3.3769 (1.3); 3.3518 (1.3); 3.3280 (1.3); 3.3054 (0.6); 3.2819 (0.6); 2.9943 (2.4); 2.9201 (2.1); 2.9045 (2.6); 2.8402 (1.0); 2.7612 (0.6); 2.7273 (16.0); 1.6548 (1.1); 1.5569 (0.4); 1.5318 (0.6); 1.5257 (0.6); 1.5034 (0.6); 1.4832 (0.5); 1.4620 (0.5); 1.2939 (0.4); 0.1071 (7.5); 0.0478 (0.5); 0.0370 (16.3); 0.0260 (0.6) 3-40: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.4025 (0.4); 8.3760 (0.4); 8.2476 (2.3); 7.8302 (0.4); 7.8158 (0.7); 7.8077 (0.8); 7.7997 (2.4); 7.7881 (2.4); 7.7721 (0.7); 7.7576 (0.4); 7.5055 (0.5); 7.4846 (0.5); 7.4621 (0.5); 7.4387 (0.3); 7.2989 (17.8); 7.2795 (0.8); 7.2651 (0.9); 7.2532 (0.4); 7.2397 (0.9); 7.0007 (1.0); 6.9570 (0.5); 6.9338 (0.4); 4.5057 (0.4); 4.4939 (0.3); 4.4731 (0.6); 4.4613 (0.5); 4.3141 (0.5); 4.3022 (0.5); 4.2815 (0.4); 4.2700 (0.4); 3.2451 (0.6); 3.2219 (1.0); 3.1942 (0.5); 2.6019 (0.4); 2.5345 (0.4); 2.4820 (0.4); 2.4498 (4.5); 2.3560 (0.3); 2.2901 (4.3); 2.0846 (0.6); 1.5856 (16.0); 1.5034 (0.6); 1.4401 (0.6); 1.3218 (0.4); 1.2983 (1.1); 1.2309 (0.7); 1.2244 (0.8); 1.2005 (0.8); 0.9201 (0.9); 0.8969 (0.4); 0.0487 (0.8); 0.0379 (22.9); 0.0272 (0.9) 3-41: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.4279 (0.4); 7.2985 (15.1); 7.2761 (0.4); 7.2733 (0.4); 7.2573 (0.6); 7.2318 (0.6); 7.1077 (0.6); 7.0821 (0.8); 6.9754 (0.7); 6.8899 (0.4); 6.8646 (0.6); 5.5893 (1.9); 4.1713 (0.6); 4.1475 (0.6); 3.8339 (0.6); 3.8232 (0.5); 3.7556 (0.5); 3.7376 (0.5); 2.9808 (1.2); 2.9557 (1.1); 2.8403 (2.7); 2.4018 (4.1); 2.3884 (6.0); 2.2488 (3.7); 2.0837 (2.6); 1.5893 (16.0); 1.4921 (0.5); 1.4293 (0.5); 1.3213 (0.9); 1.2975 (2.1); 1.2737 (0.7); 1.1826 (0.6); 1.1753 (0.6); 1.1531 (0.6); 0.9197 (1.0); 0.8967 (0.4); 0.0482 (0.6); 0.0466 (0.4); 0.0374 (18.6); 0.0297 (0.6); 0.0282 (0.6); 0.0265 (0.7) 3-42: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1996 (0.9); 8.1732 (0.9); 8.0545 (5.3); 7.8339 (1.4); 7.8243 (1.3); 7.8212 (1.6); 7.8180 (1.5); 7.8126 (2.2); 7.8047 (4.6); 7.7975 (2.1); 7.7923 (2.2); 7.7859 (4.6); 7.7773 (2.0); 7.7719 (1.6); 7.7687 (1.6); 7.7654 (1.3); 7.7560 (1.4); 7.4184 (0.6); 7.4129 (1.3); 7.4098 (1.2); 7.4041 (0.7); 7.3970 (0.7); 7.3916 (1.6); 7.3870 (2.4); 7.3814 (2.1); 7.3760 (0.7); 7.3709 (0.7); 7.3654 (1.7); 7.3590 (1.6); 7.3489 (2.2); 7.3226 (2.4); 7.2987 (8.6); 7.2334 (1.3); 7.2278 (1.2); 7.2052 (1.3); 7.2012 (1.4); 7.1788 (0.7); 7.1731 (0.7); 7.0371 (2.4); 7.0311 (2.6); 6.8929 (1.4); 6.8870 (1.3); 6.8666 (1.2); 6.8607 (1.2); 4.8357 (0.4); 4.8225 (0.6); 4.8110 (0.6); 4.7985 (0.7); 4.7852 (0.4); 4.5047 (0.8); 4.4912 (0.8); 4.4711 (1.5); 4.4577 (1.3); 4.4092 (1.4); 4.3959 (1.4); 4.3756 (0.9); 4.3622 (0.7); 4.1700 (0.9); 4.1462 (1.0); 4.1225 (0.3); 3.4251 (0.4); 3.3983 (0.4); 3.3789 (1.4); 3.3532 (2.4); 3.3312 (1.4); 3.3080 (0.4); 2.8399 (3.0); 2.7545 (0.8); 2.7171 (16.0); 2.7018 (0.6); 2.0816 (4.3); 1.8570 (0.5); 1.8458 (0.6); 1.8403 (0.4); 1.8291 (1.0); 1.8175 (0.4); 1.8121 (0.6); 1.8011 (0.6); 1.6253 (15.5); 1.3194 (1.6); 1.2957 (3.8); 1.2718 (1.3); 1.0143 (0.7); 0.9990 (1.8); 0.9924 (2.0); 0.9866 (1.1); 0.9774 (1.1); 0.9706 (2.1); 0.9643 (1.9); 0.9495 (1.0); 0.9400 (0.9); 0.9266 (0.6); 0.9181 (2.4); 0.8949 (0.8); 0.6961 (0.9); 0.6808 (2.3); 0.6750 (2.0); 0.6643 (2.0); 0.6587 (2.4); 0.6425 (0.8); 0.1072 (0.5); 0.0470 (0.4); 0.0363 (10.2); 0.0254 (0.4) 3-43: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.3440 (0.5); 8.3184 (0.5); 8.0901 (3.2); 8.0546 (1.8); 7.8260 (0.7); 7.8168 (0.6); 7.8121 (1.0); 7.8040 (1.2); 7.7965 (3.1); 7.7822 (3.1); 7.7740 (1.1); 7.7669 (0.9); 7.7611 (0.5); 7.7520 (0.7); 7.4064 (1.2); 7.3849 (1.2); 7.3826 (1.2); 7.3791 (1.8); 7.3573 (1.7); 7.2986 (8.7); 7.2724 (1.1); 7.2463 (1.3); 7.2223 (0.7); 7.2167 (0.6); 7.1969 (0.6); 7.1922 (0.8); 7.1675 (0.5); 7.1619 (0.4); 6.8919 (1.3); 6.8347 (0.7); 6.8293 (0.6); 6.8088 (0.6); 6.8035 (0.6); 4.6554 (0.4); 4.6441 (0.3); 4.6307 (0.3); 4.4946 (0.6); 4.4826 (0.5); 4.4621 (0.8); 4.4502 (0.7); 4.3183 (0.7); 4.3062 (0.7); 4.2860 (0.6); 4.2737 (0.5); 3.2420 (0.8); 3.2205 (1.4); 3.1939 (0.8); 2.9933 (16.0); 2.9209 (14.0); 2.8397 (11.7); 2.7319 (9.3); 2.7156 (0.3); 2.4989 (0.4); 2.4511 (6.5); 2.0812 (0.5); 1.8479 (0.3); 1.8309 (0.6); 1.8140 (0.4); 1.8030 (0.4); 1.6331 (14.3); 1.2955 (0.4); 0.9772 (0.4); 0.9625 (1.1); 0.9555 (1.2); 0.9493 (0.6); 0.9415 (0.6); 0.9341 (1.2); 0.9275 (1.1); 0.9136 (0.5); 0.6936 (0.5); 0.6791 (1.3); 0.6734 (1.2); 0.6625 (1.2); 0.6570 (1.3); 0.6411 (0.4); 0.0469 (0.4); 0.0360 (12.0); 0.0250 (0.4) 3-44: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.3984 (0.6); 8.3720 (0.6); 8.0900 (4.0); 7.8342 (0.7); 7.8257 (0.6); 7.8196 (1.3); 7.8117 (1.6); 7.8036 (5.0); 7.7935 (4.9); 7.7856 (1.7); 7.7777 (1.4); 7.7714 (0.6); 7.7630 (0.8); 7.4105 (1.4); 7.3897 (1.4); 7.3875 (1.6); 7.3838 (2.1); 7.3618 (2.0); 7.3390 (1.6); 7.3152 (0.4); 7.3080 (0.4); 7.3064 (0.4); 7.2989 (11.5); 7.2905 (4.9); 7.2313 (0.9); 7.2256 (0.9); 7.2061 (0.7); 7.2001 (1.0); 7.1967 (0.8); 7.1766 (0.6); 7.1708 (0.7); 4.6610 (0.5); 4.6494 (0.4); 4.6346 (0.4); 4.4844 (0.7); 4.4734 (0.7); 4.4520 (1.0); 4.4409 (0.8); 4.2953 (0.9); 4.2836 (0.9); 4.2629 (0.7); 4.2512 (0.6); 3.2448 (1.2); 3.2323 (1.2); 3.2214 (1.1); 3.2044 (1.0); 2.8413 (2.1); 2.7609 (0.4); 2.7445 (11.5); 2.7351 (1.4); 2.7245 (0.4); 2.5002 (0.8); 2.4818 (8.2); 2.4616 (0.3); 2.0827 (0.5); 1.6016 (16.0); 1.2971 (0.4); 0.0484 (0.5); 0.0452 (0.3); 0.0377 (14.5); 0.0283 (0.4); 0.0268 (0.5) 3-45: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1718 (0.6); 8.1464 (0.6); 8.0882 (3.6); 7.8403 (1.0); 7.8283 (1.0); 7.8242 (1.0); 7.8195 (1.3); 7.8110 (2.9); 7.7992 (1.5); 7.7874 (2.8); 7.7789 (1.2); 7.7744 (1.0); 7.7700 (1.1); 7.7581 (1.0); 7.4148 (0.4); 7.4094 (0.5); 7.3935 (0.5); 7.3879 (1.0); 7.3824 (0.8); 7.3772 (0.6); 7.3715 (0.5); 7.3667 (0.6); 7.3611 (0.7); 7.3550 (0.6); 7.3494 (1.1); 7.3440 (0.6); 7.3273 (0.8); 7.3217 (0.5); 7.2990 (6.6); 7.2262 (0.8); 7.2206 (0.7); 7.1988 (1.0); 7.1933 (1.0); 7.1716 (0.4); 7.1659 (0.5); 7.1479 (1.5); 7.1020 (0.6); 7.0764 (1.0); 7.0710 (0.9); 7.0080 (1.5); 6.9830 (0.9); 4.6879 (0.5); 4.6751 (0.4); 4.6630 (0.5); 4.4454 (0.5); 4.4318 (0.5); 4.4123 (1.0); 4.3988 (0.9); 4.3533 (1.0); 4.3384 (1.0); 4.3202 (0.6); 4.3054 (0.5); 3.1994 (1.8); 3.1754 (1.5); 2.7329 (10.4); 2.7168 (0.4); 2.2121 (16.0); 2.0835 (0.4); 1.6181 (11.5); 1.3208 (0.5); 1.3038 (1.5); 1.2974 (1.5); 0.9410 (0.5); 0.9192 (1.7); 0.8959 (0.6); 0.1077 (0.4); 0.0373 (8.7) 3-46: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.4217 (0.5); 8.3963 (0.4); 8.1160 (2.7); 7.8021 (0.6); 7.7941 (1.2); 7.7882 (3.5); 7.7797 (3.4); 7.7737 (1.1); 7.7656 (0.6); 7.7504 (0.4); 7.6006 (0.8); 7.5750 (0.8); 7.5548 (0.3); 7.3845 (0.5); 7.3579 (0.7); 7.2989 (14.0); 7.2675 (1.0); 7.1349 (0.5); 6.9521 (1.0); 6.8968 (1.0); 6.8501 (0.6); 6.8237 (0.5); 6.8185 (0.5); 6.7695 (0.5); 4.4934 (0.5); 4.4816 (0.4); 4.4614 (0.6); 4.4494 (0.5); 4.2989 (0.6); 4.2870 (0.6); 4.2670 (0.4); 4.2551 (0.4); 3.2496 (0.6); 3.2275 (0.6); 3.2119 (0.6); 3.1832 (0.6); 2.7408 (7.6); 2.5080 (0.4); 2.4631 (5.1); 1.8327 (0.5); 1.5932 (16.0); 0.9662 (0.9); 0.9593 (1.0); 0.9454 (0.5); 0.9378 (1.0); 0.9310 (0.9); 0.9174 (0.4); 0.6953 (0.4); 0.6812 (1.0); 0.6778 (0.9); 0.6644 (0.9); 0.6596 (0.9); 0.1071 (0.4); 0.0483 (0.7); 0.0375 (19.7); 0.0267 (0.7) 3-47: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.3569 (0.7); 8.3313 (0.7); 8.0976 (4.0); 7.8406 (1.2); 7.8305 (1.1); 7.8287 (1.2); 7.8244 (1.2); 7.8199 (1.5); 7.8117 (3.2); 7.7990 (1.7); 7.7870 (3.1); 7.7781 (1.4); 7.7737 (1.2); 7.7693 (1.3); 7.7574 (1.2); 7.6002 (0.4); 7.5739 (1.2); 7.5476 (1.0); 7.5147 (1.4); 7.4731 (1.1); 7.4445 (1.3); 7.4141 (0.6); 7.4103 (0.6); 7.2990 (4.3); 7.1499 (1.7); 7.1002 (0.6); 7.0744 (1.1); 7.0698 (1.1); 7.0207 (1.7); 6.9952 (0.9); 6.8974 (0.8); 6.7095 (1.7); 6.5216 (0.8); 5.3360 (16.0); 4.6740 (0.5); 4.6619 (0.4); 4.6498 (0.5); 4.6368 (0.3); 4.4272 (0.5); 4.4138 (0.5); 4.3946 (1.2); 4.3812 (1.1); 4.3524 (1.2); 4.3385 (1.1); 4.3198 (0.6); 4.3059 (0.5); 4.1708 (0.4); 4.1471 (0.4); 3.1812 (1.6); 3.1608 (1.2); 3.1546 (1.3); 2.7333 (11.5); 2.2146 (9.3); 2.0826 (1.7); 1.6356 (7.2); 1.3205 (0.5); 1.2967 (1.0); 1.2729 (0.5); 0.0375 (5.8) 3-48: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.5232 (0.9); 8.4975 (0.9); 8.1022 (5.3); 7.8355 (1.3); 7.8259 (1.2); 7.8227 (1.5); 7.8197 (1.5); 7.8142 (2.0); 7.8064 (4.3); 7.7993 (2.0); 7.7939 (1.9); 7.7876 (4.4); 7.7790 (1.8); 7.7735 (1.5); 7.7704 (1.5); 7.7673 (1.1); 7.7577 (1.3); 7.5992 (0.6); 7.5689 (1.3); 7.5561 (1.9); 7.5493 (2.1); 7.5472 (2.2); 7.4691 (2.6); 7.4667 (2.5); 7.4418 (1.6); 7.2989 (10.4); 7.2774 (1.8); 7.2513 (2.0); 6.9021 (2.3); 6.8439 (1.2); 6.8386 (1.0); 6.8182 (1.0); 6.8129 (1.0); 6.7087 (2.2); 6.5206 (1.1); 5.3373 (1.5); 4.6481 (0.6); 4.6373 (0.5); 4.6249 (0.5); 4.4803 (0.9); 4.4687 (0.8); 4.4483 (1.3); 4.4367 (1.1); 4.3161 (1.2); 4.3045 (1.1); 4.2841 (0.9); 4.2726 (0.8); 3.2799 (0.4); 3.2574 (0.4); 3.2337 (1.2); 3.2114 (1.2); 3.1978 (1.2); 3.1691 (1.1); 3.1515 (0.4); 3.1231 (0.4); 2.7343 (15.2); 2.4981 (0.6); 2.4534 (10.6); 2.0837 (0.6); 1.8705 (0.5); 1.8593 (0.5); 1.8426 (1.0); 1.8258 (0.6); 1.8146 (0.6); 1.6088 (16.0); 1.2976 (0.5); 0.9845 (0.6); 0.9699 (1.8); 0.9630 (2.0); 0.9487 (1.0); 0.9415 (1.9); 0.9349 (1.8); 0.9207 (0.9); 0.7009 (0.8); 0.6863 (2.1); 0.6836 (1.9); 0.6807 (2.0); 0.6696 (1.9); 0.6643 (2.1); 0.6482 (0.6); 0.0487 (0.5); 0.0471 (0.4); 0.0454 (0.4); 0.0380 (14.6); 0.0287 (0.4); 0.0271 (0.5) 3-49: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.2403 (1.0); 8.2145 (1.0); 8.1071 (5.4); 7.8289 (1.2); 7.8196 (1.0); 7.8139 (1.6); 7.8073 (2.1); 7.7989 (5.1); 7.7836 (5.0); 7.7756 (1.9); 7.7675 (1.6); 7.7632 (1.0); 7.7538 (1.3); 7.5978 (1.0); 7.5727 (1.7); 7.5562 (0.9); 7.5452 (0.9); 7.3883 (1.0); 7.3619 (1.5); 7.3344 (0.6); 7.2989 (6.9); 7.1594 (2.3); 7.1254 (1.2); 7.1120 (1.0); 7.0867 (1.6); 7.0174 (2.3); 6.9920 (1.3); 6.9428 (2.3); 6.7602 (1.1); 5.3370 (0.4); 4.6950 (0.4); 4.6816 (0.7); 4.6695 (0.6); 4.6579 (0.7); 4.6444 (0.4); 4.4392 (0.8); 4.4256 (0.8); 4.4064 (1.6); 4.3929 (1.4); 4.3396 (1.5); 4.3253 (1.4); 4.3069 (0.9); 4.2926 (0.8); 3.1997 (1.6); 3.1902 (1.8); 3.1776 (1.6); 3.1650 (1.5); 2.7392 (15.6); 2.2113 (16.0); 2.0835 (0.4); 1.6221 (3.5); 0.0482 (0.3); 0.0374 (8.8); 0.0266 (0.4) 3-50: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.4207 (1.0); 8.3941 (1.0); 8.0769 (0.6); 8.0691 (5.6); 7.8370 (1.5); 7.8272 (1.3); 7.8245 (1.5); 7.8210 (1.5); 7.8159 (2.1); 7.8077 (4.6); 7.7993 (1.9); 7.7955 (1.9); 7.7874 (4.6); 7.7789 (2.1); 7.7736 (1.6); 7.7702 (1.6); 7.7577 (1.5); 7.3195 (2.2); 7.2986 (18.0); 7.2698 (3.8); 7.2603 (2.9); 7.2550 (2.4); 7.2336 (1.7); 7.2113 (1.0); 7.2056 (0.9); 7.1531 (1.1); 7.1496 (1.0); 7.1266 (1.5); 7.1231 (1.7); 7.0998 (0.7); 7.0964 (0.7); 6.8690 (0.7); 6.8641 (0.8); 6.8421 (1.3); 6.8208 (0.6); 6.8159 (0.6); 4.6933 (0.4); 4.6812 (0.7); 4.6682 (0.6); 4.6548 (0.7); 4.6428 (0.5); 4.4692 (0.9); 4.4578 (0.9); 4.4368 (1.4); 4.4255 (1.3); 4.3388 (1.4); 4.3257 (1.4); 4.3063 (1.0); 4.2932 (0.8); 4.1718 (0.5); 4.1480 (0.5); 3.2454 (2.7); 3.2199 (2.8); 2.8416 (0.3); 2.7296 (16.0); 2.4928 (1.0); 2.4667 (11.8); 2.1654 (0.5); 2.1547 (0.5); 2.1371 (1.0); 2.1200 (0.6); 2.1088 (0.5); 2.0831 (2.2); 1.5947 (13.3); 1.3211 (0.7); 1.2973 (1.6); 1.2735 (0.6); 1.0706 (0.5); 1.0576 (1.8); 1.0508 (2.0); 1.0364 (0.9); 1.0291 (1.9); 1.0224 (1.8); 1.0095 (0.7); 0.9199 (0.6); 0.8255 (0.9); 0.8118 (1.9); 0.8080 (2.2); 0.8041 (1.8); 0.7945 (2.0); 0.7911 (1.9); 0.7867 (1.6); 0.7739 (0.7); 0.0485 (0.7); 0.0378 (22.2); 0.0269 (0.8) 3-51: ¹H-NMR(300.2 MHz, CDCl3): δ = 10.6536 (0.5); 10.6346 (0.4); 9.0611 (2.0); 9.0354 (2.0); 8.4177 (0.7); 8.4096 (0.7); 8.3715 (2.0); 8.3640 (2.0); 8.2929 (2.4); 8.2486 (12.5); 8.0699 (4.6); 8.0628 (4.7); 8.0014 (2.4); 7.8667 (1.2); 7.8563 (3.7); 7.8468 (3.3); 7.8398 (4.5); 7.8352 (4.9); 7.8268 (10.1); 7.8197 (5.4); 7.8144 (5.0); 7.8080 (10.4); 7.7993 (5.4); 7.7939 (5.3); 7.7910 (5.5); 7.7781 (4.0); 7.7573 (3.0); 7.7417 (8.2); 7.7344 (7.8); 7.7206 (1.6); 7.7119 (0.9); 7.7040 (1.2); 7.6674 (8.9); 7.6567 (16.0); 7.6407 (5.2); 7.6214 (4.2); 7.6130 (4.0); 7.6001 (1.0); 7.5914 (1.4); 7.5617 (2.8); 7.5516 (3.8); 7.5434 (3.9); 7.5325 (2.5); 7.5247 (3.1); 7.5163 (2.2); 7.4797 (0.6); 7.4728 (0.7); 7.4477 (0.4); 7.3714 (4.9); 7.3438 (4.0); 7.2992 (34.0); 7.2679 (0.9); 7.2406 (0.8); 7.1310 (2.2); 7.1036 (1.9); 5.3608 (0.3); 5.3374 (11.3); 5.3134 (0.7); 5.2960 (0.7); 5.2794 (0.4); 4.9627 (0.9); 4.9432 (1.5); 4.9202 (1.6); 4.9011 (1.0); 4.7985 (1.6); 4.7762 (0.9); 4.5436 (0.7); 4.5100 (2.9); 4.4943 (2.2); 4.4764 (3.1); 4.4603 (2.8); 4.4214 (1.2); 4.4080 (1.3); 4.3819 (0.7); 4.3680 (0.6); 4.2895 (2.8); 4.2696 (2.8); 4.2556 (2.2); 4.2357 (2.0); 4.1711 (0.5); 4.1474 (0.4); 3.7877 (0.7); 3.7551 (0.8); 3.7401 (0.9); 3.7076 (0.9); 3.5798 (0.5); 3.5445 (1.6); 3.5229 (1.9); 3.4949 (2.8); 3.4745 (2.8); 3.4086 (2.6); 3.3898 (2.7); 3.3601 (1.4); 3.3408 (1.4); 3.3267 (1.2); 3.3067 (1.1); 3.2784 (0.9); 3.2591 (0.8); 2.1179 (0.4); 2.0835 (2.4); 1.9363 (3.8); 1.7465 (0.5); 1.3204 (1.1); 1.2966 (2.0); 1.2729 (0.8); 0.9182 (0.5); 0.1068 (7.9); 0.0364 (41.2); 0.0256 (2.0) 3-52: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.4948 (0.4); 8.4696 (0.4); 8.2870 (3.1); 7.8291 (0.7); 7.8209 (1.0); 7.8146 (3.2); 7.8053 (3.0); 7.7985 (0.8); 7.7903 (0.6); 7.7147 (0.8); 7.6335 (0.5); 7.6105 (1.8); 7.5686 (0.4); 7.5592 (0.6); 7.5522 (0.4); 7.2989 (6.6); 7.0175 (1.6); 5.3378 (0.3); 4.5166 (0.5); 4.5047 (0.4); 4.4848 (0.6); 4.4729 (0.5); 4.3087 (0.5); 4.2977 (0.5); 4.2769 (0.4); 4.2660 (0.4); 3.1513 (1.0); 3.1301 (0.7); 3.1227 (0.7); 2.3596 (4.4); 2.2062 (4.3); 1.6049 (16.0); 1.3160 (1.9); 1.2951 (2.0); 0.1072 (0.9); 0.0371 (8.1) 3-53: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.3637 (0.8); 8.3378 (0.8); 8.0640 (4.8); 7.8507 (1.6); 7.8401 (1.8); 7.8340 (1.5); 7.8307 (1.8); 7.8218 (3.6); 7.8087 (0.8); 7.8003 (0.9); 7.7874 (3.6); 7.7784 (1.7); 7.7752 (1.6); 7.7693 (1.8); 7.7584 (1.7); 7.3647 (0.9); 7.3384 (2.0); 7.3123 (1.4); 7.2989 (8.6); 7.1431 (1.9); 7.0942 (0.8); 7.0635 (1.9); 7.0558 (1.2); 7.0526 (1.3); 7.0364 (1.5); 7.0326 (2.0); 7.0292 (1.9); 6.9994 (3.7); 6.9934 (2.2); 6.9745 (1.2); 4.6768 (0.6); 4.6637 (0.5); 4.6521 (0.6); 4.6380 (0.4); 4.4149 (0.6); 4.4015 (0.5); 4.3822 (1.5); 4.3689 (1.3); 4.3513 (1.4); 4.3361 (1.4); 4.3187 (0.6); 4.3035 (0.5); 3.1788 (2.3); 3.1549 (2.3); 2.8416 (2.2); 2.7147 (13.8); 2.2216 (8.9); 2.2040 (9.2); 1.9726 (0.5); 1.9613 (0.5); 1.9560 (0.4); 1.9446 (1.0); 1.9279 (0.6); 1.9165 (0.5); 1.6262 (16.0); 1.0265 (0.4); 1.0181 (0.4); 1.0102 (1.6); 1.0030 (2.0); 0.9869 (0.7); 0.9817 (1.7); 0.9750 (1.8); 0.9677 (0.5); 0.9591 (0.5); 0.7804 (0.6); 0.7763 (0.5); 0.7684 (1.2); 0.7638 (1.8); 0.7572 (1.6); 0.7513 (1.3); 0.7473 (1.6); 0.7405 (1.3); 0.7324 (0.4); 0.7285 (0.4); 0.0483 (0.4); 0.0375 (12.1); 0.0265 (0.4) 3-54: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.5469 (1.0); 8.5205 (1.0); 8.0676 (1.0); 8.0602 (5.7); 7.8510 (1.7); 7.8409 (1.6); 7.8391 (1.7); 7.8347 (1.8); 7.8303 (2.3); 7.8220 (4.4); 7.8092 (2.4); 7.7969 (4.4); 7.7882 (2.3); 7.7836 (1.8); 7.7792 (2.0); 7.7674 (1.8); 7.7607 (0.4); 7.3709 (1.2); 7.3607 (0.5); 7.3546 (0.4); 7.3438 (3.0); 7.3348 (2.6); 7.3170 (1.9); 7.3094 (0.5); 7.2988 (12.5); 7.2866 (0.6); 7.2595 (4.4); 7.2496 (2.3); 7.2278 (0.3); 7.2223 (0.3); 7.0924 (1.0); 7.0887 (1.2); 7.0849 (1.2); 7.0814 (1.4); 7.0655 (1.0); 7.0622 (1.0); 7.0577 (1.3); 7.0544 (1.2); 7.0294 (3.2); 7.0224 (2.7); 7.0149 (1.9); 7.0093 (1.7); 4.6832 (0.3); 4.6684 (0.4); 4.6567 (0.8); 4.6446 (0.6); 4.6305 (0.8); 4.6184 (0.4); 4.4502 (1.0); 4.4394 (0.9); 4.4182 (1.4); 4.4075 (1.3); 4.3190 (1.4); 4.3067 (1.4); 4.2870 (1.0); 4.2748 (0.9); 3.2324 (0.4); 3.2132 (3.2); 3.1874 (3.1); 2.8411 (0.7); 2.7410 (1.1); 2.7233 (16.0); 2.4856 (1.2); 2.4598 (11.8); 2.2927 (0.8); 2.0835 (0.7); 1.9736 (0.6); 1.9623 (0.6); 1.9454 (1.2); 1.9289 (0.7); 1.9175 (0.6); 1.9006 (0.3); 1.6163 (14.1); 1.3208 (0.4); 1.2971 (1.2); 1.0204 (0.4); 1.0023 (1.8); 0.9995 (1.7); 0.9949 (2.7); 0.9735 (1.9); 0.9671 (2.6); 0.9493 (0.5); 0.9410 (0.4); 0.9305 (0.4); 0.9189 (1.1); 0.8956 (0.4); 0.7806 (0.9); 0.7721 (1.7); 0.7664 (1.4); 0.7628 (1.7); 0.7554 (2.8); 0.7497 (1.5); 0.7455 (1.5); 0.7388 (1.3); 0.7319 (0.6); 0.0478 (0.6); 0.0370 (16.8); 0.0277 (0.5); 0.0261 (0.6) 3-55: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.5228 (1.1); 8.4966 (1.0); 8.0672 (5.6); 7.8426 (1.7); 7.8325 (1.8); 7.8310 (1.8); 7.8261 (1.7); 7.8221 (2.1); 7.8139 (4.3); 7.7996 (2.0); 7.7861 (4.4); 7.7769 (2.1); 7.7729 (1.8); 7.7681 (2.0); 7.7565 (1.8); 7.3648 (1.0); 7.3385 (2.1); 7.3109 (1.4); 7.2987 (10.3); 7.2639 (2.0); 7.2378 (2.2); 7.0978 (1.0); 7.0924 (1.4); 7.0866 (1.3); 7.0706 (0.8); 7.0675 (0.9); 7.0629 (1.2); 7.0600 (1.1); 7.0339 (4.0); 7.0296 (4.0); 7.0063 (1.4); 6.8969 (2.3); 6.8129 (1.2); 6.8075 (1.2); 6.7868 (1.1); 6.7815 (1.1); 4.6642 (0.4); 4.6520 (0.7); 4.6391 (0.6); 4.6262 (0.7); 4.6144 (0.5); 4.4616 (0.9); 4.4498 (0.9); 4.4297 (1.4); 4.4181 (1.3); 4.3314 (1.4); 4.3190 (1.3); 4.2995 (1.0); 4.2871 (0.8); 3.2070 (3.0); 3.1814 (2.5); 2.8416 (7.2); 2.7155 (16.0); 2.4865 (0.7); 2.4415 (11.5); 1.9708 (0.6); 1.9596 (0.6); 1.9428 (1.2); 1.9260 (0.7); 1.9150 (0.6); 1.8979 (0.4); 1.8677 (0.5); 1.8564 (0.6); 1.8397 (1.1); 1.8229 (0.6); 1.8118 (0.6); 1.7950 (0.3); 1.6244 (10.6); 1.3036 (0.9); 1.0163 (0.4); 0.9985 (1.9); 0.9916 (2.5); 0.9789 (1.0); 0.9638 (4.3); 0.9576 (2.6); 0.9431 (1.5); 0.9360 (2.3); 0.9292 (2.2); 0.9193 (1.4); 0.9154 (1.2); 0.8963 (0.5); 0.7815 (0.7); 0.7716 (1.5); 0.7644 (1.8); 0.7562 (2.3); 0.7489 (1.7); 0.7408 (1.3); 0.7295 (0.5); 0.6984 (0.9); 0.6837 (2.4); 0.6783 (2.2); 0.6671 (2.1); 0.6617 (2.4); 0.6455 (0.7); 0.0482 (0.5); 0.0374 (14.2); 0.0283 (0.5); 0.0266 (0.5) 3-56: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.0711 (1.7); 7.8298 (0.3); 7.8156 (0.5); 7.8077 (0.6); 7.7993 (1.8); 7.7872 (1.8); 7.7790 (0.6); 7.7710 (0.5); 7.7569 (0.4); 7.6027 (0.5); 7.5814 (0.4); 7.3644 (0.8); 7.3382 (0.8); 7.2990 (8.4); 7.1563 (0.7); 7.1325 (0.3); 7.0032 (0.4); 6.9773 (0.4); 6.9497 (0.7); 6.7672 (0.4); 4.4789 (0.5); 4.4657 (0.4); 4.4002 (0.5); 4.3871 (0.5); 3.3939 (0.4); 3.3669 (0.5); 3.3582 (0.5); 3.3345 (0.4); 2.7221 (4.9); 2.2891 (3.4); 2.0839 (0.8); 1.5977 (16.0); 1.3212 (0.4); 1.2975 (1.0); 0.9193 (0.7); 0.1068 (0.9); 0.0479 (0.4); 0.0372 (9.9); 0.0263 (0.3) 3-57: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.3646 (1.0); 8.3387 (1.0); 8.2237 (7.2); 7.8349 (1.5); 7.8253 (1.3); 7.8219 (1.7); 7.8191 (1.5); 7.8135 (2.2); 7.8060 (4.8); 7.7992 (2.1); 7.7934 (2.1); 7.7876 (4.8); 7.7789 (1.9); 7.7733 (1.8); 7.7702 (1.5); 7.7670 (1.1); 7.7575 (1.4); 7.5206 (0.4); 7.2983 (23.6); 7.2640 (0.8); 7.2582 (0.9); 7.2513 (2.0); 7.2367 (1.5); 7.2311 (1.5); 7.2260 (2.3); 7.2141 (1.1); 7.2084 (0.9); 7.1632 (1.0); 7.1367 (1.5); 7.1334 (1.5); 7.1103 (0.8); 7.1068 (0.8); 6.9868 (2.2); 6.9327 (1.2); 6.9066 (1.1); 6.8915 (0.8); 6.8697 (1.3); 6.8488 (0.7); 5.3375 (16.0); 4.6831 (0.4); 4.6712 (0.8); 4.6584 (0.7); 4.6455 (0.8); 4.6330 (0.5); 4.4989 (1.0); 4.4868 (0.8); 4.4660 (1.5); 4.4540 (1.2); 4.3459 (1.4); 4.3333 (1.3); 4.3131 (1.0); 4.3006 (0.9); 4.1721 (0.7); 4.1485 (0.5); 3.2379 (2.8); 3.2123 (2.2); 2.6030 (1.6); 2.5349 (1.4); 2.4806 (0.6); 2.4386 (11.3); 2.3741 (0.7); 2.3526 (0.5); 2.2848 (10.7); 2.2403 (0.6); 2.1671 (0.5); 2.1559 (0.5); 2.1388 (1.0); 2.1219 (0.6); 2.1102 (0.5); 2.0925 (0.4); 2.0833 (2.5); 1.5871 (15.9); 1.3214 (0.9); 1.2976 (2.1); 1.2738 (0.7); 1.0900 (0.4); 1.0864 (0.4); 1.0749 (1.8); 1.0678 (2.0); 1.0573 (1.0); 1.0523 (0.8); 1.0462 (1.9); 1.0396 (1.9); 1.0282 (0.6); 1.0245 (0.6); 0.9203 (0.8); 0.8352 (0.9); 0.8180 (2.0); 0.8135 (1.8); 0.8042 (1.9); 0.7964 (1.5); 0.7843 (0.7); 0.1079 (2.9); 0.0490 (0.9); 0.0473 (0.6); 0.0382 (23.5); 0.0305 (0.8); 0.0290 (0.8); 0.0273 (0.9) 3-58: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.4089 (1.0); 8.3832 (1.0); 8.1117 (5.6); 7.8165 (0.8); 7.8090 (0.6); 7.8016 (1.6); 7.7935 (2.4); 7.7870 (7.7); 7.7777 (7.5); 7.7713 (2.3); 7.7630 (1.6); 7.7556 (0.6); 7.7481 (0.9); 7.6273 (0.6); 7.6017 (1.7); 7.5756 (1.7); 7.5542 (0.7); 7.3861 (1.0); 7.3593 (1.5); 7.3327 (0.6); 7.2990 (2.8); 7.2878 (1.9); 7.2623 (2.2); 7.1323 (1.1); 6.9952 (2.3); 6.9499 (2.9); 6.9332 (1.1); 6.7669 (1.1); 5.3337 (6.3); 4.6801 (0.4); 4.6678 (0.6); 4.6563 (0.6); 4.6453 (0.6); 4.6317 (0.4); 4.5022 (1.0); 4.4903 (1.0); 4.4700 (1.4); 4.4582 (1.2); 4.3107 (1.2); 4.2987 (1.3); 4.2785 (1.0); 4.2666 (0.9); 3.3047 (0.4); 3.2822 (0.4); 3.2586 (1.3); 3.2361 (1.3); 3.2247 (1.4); 3.1961 (1.2); 3.1785 (0.4); 3.1500 (0.4); 2.7365 (16.0); 2.4601 (11.4); 2.2850 (10.8); 1.6740 (2.9); 0.0374 (3.8)

TABLE 9 Compounds according to formula (4)

(4) In table 9, ″#″ denotes the point of attachment to the L-R⁶ group and ″*″ denotes the point of attachment to the pyridazin-4-yl group. Ex No R⁷ R⁸ Q

L-R⁶ LogP 4-01 CH₃ H 3-(trifluoro- methyl)phenyl

2,4-dichlorophenyl 3.29^([a]); 3.36^([b]) 4-02 Cl H 3-(trifluoro- methyl)phenyl

2,4-dichlorophenyl 3.76[a]; 3.82[b] 4-03 Cl H 3-cyclopropyl-2- fluorophenyl

(2,4-dimethyl- phenyl)methyl 3.46^([a]) 4-04 Cl H 3-(difluoromethyl)-2- fluorophenyl

(2,4-dimethyl- phenyl)methyl 3.02^([a]) 4-05 CH₃ H 3-cyclopropyl-2- fluorophenyl

(4-bromo-2-chloro- phenyl)methyl 3.17^([a]) 4-06 Cl CH₃ 3-(trifluoro- methyl)phenyl

(2,4-dimethyl- phenyl)methyl 3.06[a] 4-07 CH₃ H 3-cyclopropylphenyl

(2,4-dimethyl- phenyl)methyl 2.69^([a]) 4-08 I H 3-(trifluor- omethyl)phenyl

(2,4-dimethyl- phenyl)methyl 3.37^([a]) 4-09 CH₃ H 3-cyclopropyl-2- fluorophenyl

(2,4-dimethyl- phenyl)methyl 2.90^([a]) 4-10 Cl H 3-(trifluoro- methyl)phenyl

(3,4-dimethyl- phenyl)methyl 3.25^([a]) 4-11 Cl H 3-(trifluoro- methyl)phenyl

(2,4-dichloro- phenyl)methyl 3.51^([a]) 4-12 Cl H 3-(trifluoro- methyl)phenyl

(4-cyclopropyl-2-methyl- phenyl)methyl 3.59^([a]) 4-13 Cl H 3-(trifluoro- methyl)phenyl

(2-chloro-4-cyclopropyl- phenyl)methyl 3.68^([a]) 4-14 Cl H 3-(trifluoro- methyl)phenyl

(2-chloro-4-isopropyl- phenyl)methyl 4.01^([a]) 4-15 Cl H 3-(trifluoro- methyl)phenyl

(4-isopropyl-2-methyl- phenyl)methyl 3.94^([a]) 4-16 CH₃ H 3-cyclopropyl-2- fluorophenyl

(3,4-dimethyl- phenyl)methyl 2.78^([a]) 4-17 Cl H 3-(trifluoro- methyl)phenyl

(2,4-dimethyl- phenyl)methyl 3.37^([a]) 4-18 Cl H 3-(trifluoro- methyl)phenyl

(4-chlorophenyl)methyl 3.18^([a]); 3.42^([b]) 4-19 CH₃ CH₃ 3-(trifluoro- methyl)phenyl

(2,4-dimethyl- phenyl)methyl 2.51^([a]) 4-20 CH₃ H 3-(difluoro- methyl)phenyl

(2,4-dimethyl- phenyl)methyl 2.40^([a]) 4-21 Cl H 3-(trifluoro- methyl)phenyl

(4-bromo-2-chloro- phenyl)methyl 3.63^([a]) 4-22 Cl H 3-(trifluoro- methyl)phenyl

(4-bromo-2-methyl- phenyl)methyl 3.55^([a]) 4-23 Cl H 5-bromopyridin-3-yl

(2,4-dimethyl- phenyl)methyl 2.50^([a]) 4-24 Cl H 6-chloro-5-(trifluoro- methyl)pyridin-3-yl

(2,4-dimethyl- phenyl)methyl 3.37^([a]) 4-25 Cl CH₃ 3-cyclopropyl-2- fluorophenyl

(4-bromo-2- chlorophenyl)methyl 3.41^([a]) 4-26 Cl CH₃ 3-cyclopropyl-2- fluorophenyl

(2-chloro-4-cyclo- propylphenyl)methyl 3.46^([a]) 4-27 Cl H 3-cyclopropylphenyl

(2,4-dimethyl- phenyl)methyl 3.39^([a]) 4-28 Cl H 3-(1-fluoro- cyclopropyl)phenyl

(2,4-dimethyl- phenyl)methyl 3.27^([a]) 4-29 CH₃ H 3-cyclopropyl-2- fluorophenyl

(2-chloro-4-cyclopropyl- phenyl)methyl 3.21^([a]) 4-30 Cl CH₃ 3-cyclopropyl-2- fluorophenyl

(2,4-dichloro- phenyl)methyl 3.33^([a]) 4-31 Cl H 3-cyclopropylphenyl

(2,4-dichloro- phenyl)methyl 3.68^([a]) 4-32 Cl H 2-fluoro-3-[rac-2,2- difluoro- cyclopropyl]phenyl

(2,4-dimethyl- phenyl)methyl 3.23^([a]) 4-33 CH₃ H 3-(trifluoro- methyl)phenyl

(2,4-dimethyl- phenoxy)methyl 3.13^([a]) 4-34 CH₃ H 3-(trifluoro- methyl)phenyl

(4-chlorophenoxy)methyl 2.88^([a]) 4-35 Cl H 3-(trifluoro- methyl)phenyl

[(2,4-dimethyl- phenyl)thio]methyl 4.76^([a]) 4-36 Cl CH₃ 2-fluoro-3-[rac-2,2- difluoro- cyclopropyl]phenyl

(2,4-dimethyl- phenyl)methyl 3.03^([a]) 4-37 CH₃ H 2-fluoro-3-(trifluoro- methyl)phenyl

(2,4-dimethyl- phenyl)methyl 2.88^([a]) 4-38 CH₃ H 2-fluoro-3-(trifluoro- methyl)phenyl

(2,4-dichloro- phenyl)methyl 3.04^([a]) 4-39 CH₃ H 3-(difluoro- methyl)phenyl

(2,4-dichloro- phenyl)methyl 2.61^([a]) 4-40 Cl H 2-fluoro-3-(1-fluoro- cyclopropyl)phenyl

(2,4-dimethyl- phenyl)methyl 3.28^([a]) 4-41 Cl CH₃ 2-fluoro-3-(1-fluoro- cyclopropyl)phenyl

(2,4- dimethylphenyl)methyl 3.01^([a]) 4-42 CH₃ H 3-chloro-2- fluorophenyl

(2-chloro-4-cyclo- propylphenyl)methyl 3.01^([a]) 4-43 CH₃ H 3-chloro-2- fluorophenyl

(4-cyclopropyl-2- methylphenyl)methyl 2.91^([a]) 4-44 CH₃ H 3-chloro-2- fluorophenyl

(4-bromo-2-methyl- phenyl)methyl 2.86^([a]) 4-45 CH₃ H 3-chloro-2- fluorophenyl

(3,4-dimethyl- phenyl)methyl 2.65^([a]) 4-46 CH₃ H 3-(difluoromethyl)-2- fluorophenyl

(4-cyclopropyl-2- methylphenyl)methyl 2.83^([a]) 4-47 CH₃ H 3-(difluoro- methyl)phenyl

(3,4-dimethyl- phenyl)methyl 2.44^([a]) 4-48 CH₃ H 3-(difluoro- methyl)phenyl

(4-cyclopropyl-2- methylphenyl)methyl 2.73^([a]) 4-49 CH₃ H 3-(difluoromethyl)-2- fluorophenyl

(2,4-dimethyl- phenyl)methyl 2.59^([a]) 4-50 CH₃ H 3-(difluoromethyl)-2- fluorophenyl

(3,4-dimethyl- phenyl)methyl 2.51^([a]) 4-51 CH₃ H 3-cyclopropyl-2- fluorophenyl

(4-bromo-2-methyl- phenyl)methyl 3.08^([a]) 4-52 Cl H 3-(trifluoro- methyl)phenyl

(5-chloropyridin-2- yl)methyl 2.50^([a]) 4-53 Cl H 3-(trifluoro- methyl)phenyl

(4,5-dimethyl-3- thienyl)methyl 3.24^([a]) 4-54 CH₃ H 3-cyclopropylphenyl

(3,4-dimethyl- phenyl)methyl 2.83^([a]) 4-55 CH₃ H 3-cyclopropylphenyl

(4-bromo-2-methyl- phenyl)methyl 3.10^([a]) 4-56 CH₃ H 3-cyclopropylphenyl

(2-chloro-4-cyclopropyl- phenyl)methyl 3.25^([a]) 4-57 CH₃ H 3-(difluoromethyl)-2- fluorophenyl

(2-chloro-4-methyl- phenyl)methyl 2.67^([a])

TABLE 10 4-01: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 9.4264 (1.4); 9.4079 (1.4); 7.8269 (5.7); 7.7301 (0.7); 7.7105 (1.9); 7.6908 (1.6); 7.6581 (3.5); 7.6362 (1.1); 7.6128 (4.2); 7.6074 (4.2); 7.5899 (1.5); 7.5714 (1.0); 7.5396 (2.2); 7.5185 (2.6); 7.3288 (1.8); 7.3235 (1.8); 7.3078 (1.5); 7.3025 (1.5); 5.6745 (0.5); 5.6565 (1.2); 5.6435 (1.0); 5.6382 (0.8); 5.6253 (0.5); 3.7626 (0.4); 3.7466 (2.1); 3.7428 (2.1); 3.7352 (1.8); 3.7239 (1.5); 3.6958 (0.3); 3.4354 (0.3); 3.3975 (0.4); 3.3754 (0.4); 3.3686 (0.5); 3.3433 (0.5); 3.3158 (0.4); 2.6756 (0.4); 2.6709 (0.5); 2.6663 (0.4); 2.6181 (16.0); 2.5242 (1.4); 2.5194 (2.2); 2.5107 (29.1); 2.5064 (57.5); 2.5018 (75.0); 2.4973 (55.0); 2.4930 (27.3); 2.3330 (0.3); 2.3287 (0.5); 2.3242 (0.4); 2.0737 (0.4); 0.1461 (0.4); 0.1230 (0.4); 0.0080 (2.6); −0.0002 (82.1); −0.0085 (3.1); −0.1495 (0.4) 4-02: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 9.5104 (2.8); 9.4918 (2.8); 8.3144 (0.7); 8.1803 (16.0); 7.7577 (1.1); 7.7380 (3.4); 7.7234 (4.6); 7.7195 (6.1); 7.6939 (3.8); 7.6749 (1.7); 7.6429 (2.6); 7.6173 (7.8); 7.6120 (7.2); 7.5398 (4.9); 7.5187 (6.0); 7.3351 (3.5); 7.3298 (3.4); 7.3141 (2.9); 7.3087 (2.9); 5.7543 (5.1); 5.6710 (0.9); 5.6592 (1.1); 5.6523 (2.1); 5.6403 (1.9); 5.6337 (1.3); 5.6215 (0.9); 3.7807 (0.9); 3.7686 (1.2); 3.7524 (3.5); 3.7393 (4.9); 3.7187 (3.1); 3.7099 (1.1); 3.6907 (1.1); 3.3237 (59.5); 2.6797 (0.7); 2.6753 (1.5); 2.6707 (2.1); 2.6662 (1.5); 2.6617 (0.7); 2.6176 (0.5); 2.5242 (6.6); 2.5194 (10.0); 2.5108 (126.0); 2.5063 (250.8); 2.5018 (328.0); 2.4972 (239.8); 2.4928 (118.0); 2.3377 (0.8); 2.3331 (1.6); 2.3286 (2.1); 2.3241 (1.6); 2.3198 (0.7); 2.0735 (1.3); 0.1461 (1.7); 0.0184 (0.5); 0.0080 (13.0); −0.0002 (382.0); −0.0085 (14.4); −0.1494 (1.7) 4-03: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.4942 (1.0); 8.4682 (1.0); 8.2884 (8.9); 7.2986 (24.3); 7.1809 (0.6); 7.1539 (2.0); 7.1281 (4.0); 7.1238 (2.5); 7.1104 (1.5); 7.1041 (1.9); 7.0849 (2.8); 7.0598 (3.1); 6.9700 (2.9); 6.9075 (1.0); 6.8859 (3.0); 6.8789 (1.6); 6.8608 (2.0); 5.5759 (5.8); 5.3377 (10.9); 4.6628 (0.5); 4.6524 (0.6); 4.6452 (0.7); 4.6349 (0.8); 4.6255 (0.7); 4.6189 (0.6); 4.6075 (0.6); 3.8733 (1.2); 3.8622 (1.2); 3.8352 (2.4); 3.8241 (2.2); 3.7703 (2.2); 3.7520 (2.1); 3.7321 (1.2); 3.7139 (1.1); 3.0017 (4.7); 2.9773 (4.6); 2.6036 (0.5); 2.5355 (0.4); 2.4075 (16.0); 2.3743 (0.4); 2.2727 (14.8); 2.2402 (0.4); 2.1933 (0.4); 2.1756 (0.6); 2.1650 (0.7); 2.1475 (1.3); 2.1304 (0.8); 2.1190 (0.7); 2.1023 (0.4); 2.0836 (0.8); 1.5892 (13.4); 1.3218 (0.4); 1.2977 (0.9); 1.1173 (1.0); 1.1024 (2.4); 1.0954 (2.7); 1.0807 (1.6); 1.0738 (2.6); 1.0671 (2.5); 1.0525 (1.2); 0.8495 (1.3); 0.8344 (3.0); 0.8285 (2.9); 0.8174 (2.7); 0.8121 (3.1); 0.7956 (1.0); 0.1080 (4.1); 0.0493 (0.9); 0.0385 (23.5); 0.0276 (0.9) 4-04: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.3531 (0.8); 8.3266 (0.9); 8.3029 (9.1); 8.2979 (1.4); 7.6447 (0.8); 7.6209 (1.3); 7.6017 (0.8); 7.4923 (0.6); 7.4684 (1.3); 7.4480 (1.0); 7.4415 (0.8); 7.4208 (1.9); 7.3936 (2.0); 7.3667 (0.7); 7.2987 (15.0); 7.1293 (1.5); 7.0969 (0.3); 7.0763 (2.1); 7.0507 (2.7); 6.9910 (0.5); 6.9656 (2.5); 6.9472 (3.1); 6.8896 (1.5); 6.8637 (1.1); 6.7649 (1.5); 5.5723 (2.6); 5.3374 (16.0); 4.6678 (0.5); 4.6569 (0.5); 4.6500 (0.6); 4.6403 (0.7); 4.6303 (0.6); 4.6233 (0.6); 4.6124 (0.5); 4.1731 (0.4); 4.1678 (0.3); 3.8756 (1.0); 3.8646 (1.1); 3.8373 (2.2); 3.8263 (2.0); 3.7736 (2.0); 3.7555 (2.0); 3.7353 (1.0); 3.7172 (1.0); 3.0308 (0.5); 3.0077 (4.3); 2.9834 (4.1); 2.4224 (2.0); 2.4021 (14.3); 2.2882 (2.0); 2.2628 (13.1); 2.0092 (0.4); 1.7645 (2.2); 1.6738 (1.5); 1.5973 (4.0); 1.2976 (0.5); 0.9950 (0.4); 0.9916 (0.6); 0.9694 (1.0); 0.9667 (1.3); 0.9416 (0.6); 0.1087 (1.3); 0.0496 (0.6); 0.0387 (16.6); 0.0279 (0.5) 4-05: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.3293 (0.7); 8.3029 (0.7); 8.0813 (3.9); 8.0578 (0.4); 7.9229 (0.4); 7.9124 (0.4); 7.9050 (0.4); 7.8949 (0.5); 7.7956 (0.6); 7.7854 (0.4); 7.7782 (0.4); 7.5138 (2.0); 7.5075 (2.0); 7.2993 (27.9); 7.2652 (1.5); 7.2593 (1.5); 7.2107 (2.5); 7.1835 (1.3); 7.1500 (2.7); 7.1328 (2.0); 7.1256 (2.2); 6.8830 (0.5); 6.8625 (0.8); 6.8513 (0.9); 6.8393 (0.5); 6.8296 (0.4); 5.6053 (2.6); 5.3384 (9.3); 4.8221 (0.5); 4.8139 (0.5); 4.7902 (0.3); 4.1798 (0.6); 3.9277 (0.7); 3.9160 (0.7); 3.8904 (1.2); 3.8782 (1.1); 3.8037 (1.2); 3.7848 (1.1); 3.7659 (0.7); 3.7471 (0.7); 3.1483 (0.3); 3.1240 (1.5); 3.1126 (1.5); 3.1019 (1.4); 3.0864 (1.3); 2.9947 (2.6); 2.9225 (2.4); 2.8422 (13.2); 2.7308 (11.6); 2.1745 (0.4); 2.1637 (0.5); 2.1461 (0.8); 2.1297 (0.5); 2.1184 (0.5); 1.5902 (16.0); 1.1037 (0.5); 1.0877 (1.4); 1.0818 (1.6); 1.0667 (0.9); 1.0593 (1.5); 1.0531 (1.6); 1.0389 (0.7); 0.8430 (0.6); 0.8220 (1.9); 0.8109 (1.7); 0.8049 (2.0); 0.7888 (0.6); 0.1076 (0.4); 0.0384 (33.0) 4-06: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.5743 (1.6); 7.5543 (4.2); 7.5518 (3.7); 7.4635 (2.0); 7.4208 (0.8); 7.4106 (1.2); 7.4032 (1.0); 7.3903 (0.8); 7.3822 (0.4); 7.2991 (5.8); 7.1002 (1.8); 7.0746 (2.2); 6.9869 (2.2); 6.8936 (1.3); 6.8681 (1.0); 6.7547 (0.9); 6.7260 (1.0); 5.5895 (1.4); 5.3373 (0.5); 4.7540 (0.4); 4.7436 (0.4); 4.7352 (0.5); 4.7252 (0.6); 4.7152 (0.5); 4.7066 (0.4); 4.6994 (0.4); 3.8770 (0.9); 3.8660 (0.9); 3.8389 (1.6); 3.8281 (1.4); 3.7527 (1.4); 3.7334 (1.4); 3.7147 (0.8); 3.6954 (0.8); 2.9608 (2.8); 2.9359 (2.5); 2.3908 (12.0); 2.3557 (16.0); 2.2590 (11.0); 1.6273 (1.7); 1.2959 (0.4); 0.9197 (0.3); 0.0380 (5.9) 4-07: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.5484 (0.8); 8.5220 (0.8); 8.1316 (5.3); 7.3789 (1.2); 7.3527 (2.6); 7.3264 (1.6); 7.2985 (8.9); 7.0784 (1.8); 7.0528 (2.3); 7.0303 (1.5); 7.0042 (1.4); 6.9990 (1.3); 6.9972 (1.4); 6.9938 (1.2); 6.9887 (1.5); 6.9856 (1.5); 6.9726 (2.4); 6.9621 (1.4); 6.9326 (1.8); 6.9265 (2.2); 6.9197 (1.2); 6.8903 (1.2); 6.8640 (0.9); 5.5661 (3.3); 5.3373 (4.8); 4.6634 (0.4); 4.6523 (0.4); 4.6455 (0.5); 4.6356 (0.6); 4.6260 (0.5); 4.6188 (0.4); 4.6081 (0.4); 3.8555 (0.8); 3.8440 (0.8); 3.8179 (1.7); 3.8065 (1.5); 3.7563 (1.6); 3.7378 (1.5); 3.7187 (0.8); 3.7002 (0.8); 2.9746 (3.4); 2.9502 (3.3); 2.8414 (1.0); 2.7284 (16.0); 2.4032 (11.7); 2.2843 (10.8); 1.9859 (0.6); 1.9745 (0.6); 1.9578 (1.1); 1.9411 (0.6); 1.9300 (0.6); 1.6272 (4.9); 1.0670 (0.7); 1.0521 (1.9); 1.0451 (2.1); 1.0304 (1.1); 1.0237 (2.0); 1.0169 (1.8); 1.0025 (0.9); 0.7874 (0.9); 0.7723 (2.4); 0.7662 (2.0); 0.7558 (2.0); 0.7504 (2.4); 0.7340 (0.7); 0.0480 (0.4); 0.0372 (9.5); 0.0264 (0.3) 4-08: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.5851 (2.9); 8.3666 (0.4); 8.3414 (0.4); 8.0516 (1.9); 7.6494 (1.5); 7.6325 (2.0); 7.4774 (1.1); 7.4438 (0.5); 7.4354 (0.5); 7.4294 (0.6); 7.4230 (0.6); 7.4138 (0.5); 7.4064 (0.3); 7.2991 (5.9); 7.0597 (0.9); 7.0341 (1.2); 6.9704 (1.4); 6.8836 (0.7); 6.8586 (0.6); 5.5622 (0.6); 5.3360 (3.0); 4.6248 (0.4); 3.8703 (0.4); 3.8593 (0.5); 3.8320 (0.8); 3.8211 (0.8); 3.7676 (0.8); 3.7496 (0.8); 3.7294 (0.5); 3.7114 (0.4); 2.9928 (16.0); 2.9685 (2.0); 2.9189 (12.9); 2.8535 (0.6); 2.8398 (12.6); 2.5989 (0.9); 2.5341 (0.8); 2.4302 (0.4); 2.3931 (6.0); 2.3705 (1.0); 2.3247 (0.6); 2.3156 (0.7); 2.2994 (0.5); 2.2723 (5.7); 2.2366 (0.8); 1.2893 (0.4); 0.1063 (0.6); 0.0355 (7.4); 0.0250 (0.6) 4-09: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.4893 (0.7); 8.4622 (0.7); 8.1340 (5.3); 7.2986 (10.2); 7.1365 (3.4); 7.1187 (2.5); 7.1142 (2.0); 7.1083 (1.7); 7.0964 (1.8); 7.0708 (2.1); 6.9661 (2.0); 6.8878 (1.2); 6.8740 (0.8); 6.8578 (1.7); 6.8429 (1.1); 6.8290 (0.6); 6.8202 (0.5); 5.5930 (4.3); 5.3376 (6.4); 4.6797 (0.4); 4.6686 (0.4); 4.6615 (0.5); 4.6519 (0.5); 4.6418 (0.4); 4.6346 (0.4); 4.6237 (0.4); 3.8724 (0.8); 3.8609 (0.8); 3.8347 (1.6); 3.8232 (1.5); 3.7705 (1.5); 3.7517 (1.5); 3.7328 (0.8); 3.7140 (0.8); 2.9963 (3.2); 2.9720 (3.1); 2.8413 (0.4); 2.7316 (16.0); 2.4111 (11.1); 2.2693 (10.3); 2.1737 (0.5); 2.1624 (0.5); 2.1454 (1.0); 2.1281 (0.5); 2.1172 (0.5); 1.6214 (7.0); 1.0988 (0.7); 1.0841 (1.7); 1.0770 (1.9); 1.0708 (1.0); 1.0624 (1.1); 1.0555 (1.8); 1.0487 (1.7); 1.0342 (0.8); 0.8393 (0.9); 0.8244 (2.0); 0.8217 (1.9); 0.8184 (2.0); 0.8074 (1.8); 0.8020 (2.1); 0.7856 (0.7); 0.1072 (1.5); 0.0479 (0.4); 0.0371 (10.7); 0.0262 (0.4) 4-10: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.3120 (8.0); 8.1748 (0.9); 8.1483 (0.9); 8.1096 (0.4); 7.6560 (4.2); 7.6387 (4.1); 7.5841 (0.4); 7.4593 (2.3); 7.4293 (0.4); 7.4171 (1.0); 7.4088 (1.0); 7.3996 (1.4); 7.3929 (1.2); 7.3867 (0.9); 7.3784 (0.6); 7.2986 (15.0); 7.0095 (3.2); 6.9479 (7.9); 6.9448 (7.9); 5.5944 (2.4); 5.3373 (5.2); 4.7284 (0.5); 4.7159 (0.6); 4.7062 (0.7); 4.6940 (0.7); 4.6894 (0.7); 4.6799 (0.6); 4.6677 (0.5); 3.8849 (1.2); 3.8729 (1.2); 3.8467 (2.2); 3.8347 (2.0); 3.7582 (2.0); 3.7375 (1.9); 3.7200 (1.2); 3.6993 (1.1); 2.9561 (2.7); 2.9511 (2.7); 2.9306 (3.1); 2.2886 (0.7); 2.2781 (0.8); 2.1918 (16.0); 2.1817 (15.7); 1.6069 (2.1); 1.2931 (0.4); 0.1082 (1.2); 0.0490 (0.6); 0.0383 (19.0); 0.0273 (0.7) 4-11: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.3034 (1.9); 8.2671 (16.0); 8.0569 (0.6); 7.8932 (0.3); 7.7950 (0.4); 7.6958 (0.5); 7.6681 (5.2); 7.6627 (3.8); 7.6507 (9.6); 7.5985 (0.6); 7.5021 (4.5); 7.4706 (1.0); 7.4569 (2.0); 7.4431 (2.7); 7.4369 (2.7); 7.4270 (2.1); 7.4186 (1.4); 7.3549 (6.5); 7.3479 (6.8); 7.2986 (39.9); 7.2800 (4.8); 7.2643 (0.8); 7.2525 (8.0); 7.2318 (0.4); 7.1838 (5.0); 7.1768 (4.6); 7.1563 (2.8); 7.1494 (2.6); 5.5747 (10.3); 5.3375 (4.8); 4.8424 (0.3); 4.8153 (1.0); 4.8006 (1.2); 4.7900 (1.5); 4.7635 (1.1); 4.7468 (0.5); 4.7347 (0.4); 4.3179 (0.5); 3.9240 (2.3); 3.9127 (2.4); 3.9000 (0.4); 3.8857 (4.3); 3.8745 (3.9); 3.7995 (3.9); 3.7815 (3.9); 3.7611 (2.4); 3.7432 (2.2); 3.2068 (1.0); 3.1809 (1.0); 3.1603 (4.4); 3.1359 (6.7); 3.1144 (4.2); 3.0912 (1.0); 3.0678 (0.8); 1.5910 (12.7); 1.2941 (0.9); 0.1073 (2.1); 0.0485 (1.7); 0.0377 (51.4); 0.0267 (1.8) 4-12: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.4370 (1.1); 8.4102 (1.0); 8.3174 (8.6); 8.1076 (0.4); 7.6916 (0.3); 7.6629 (3.5); 7.6456 (5.4); 7.5911 (0.4); 7.5393 (0.4); 7.5044 (2.6); 7.4686 (0.6); 7.4555 (1.3); 7.4475 (1.1); 7.4410 (1.7); 7.4346 (1.5); 7.4254 (1.1); 7.4171 (0.8); 7.2986 (19.3); 7.1630 (0.4); 7.1519 (0.4); 7.1072 (0.6); 7.0807 (0.5); 7.0655 (2.5); 7.0395 (3.0); 6.8983 (0.5); 6.8726 (3.3); 6.7781 (1.7); 6.7725 (1.6); 6.7520 (1.4); 6.7465 (1.3); 5.5561 (0.5); 5.3378 (12.9); 4.6404 (0.6); 4.6227 (0.7); 4.6138 (0.8); 4.6047 (0.7); 4.5892 (0.6); 4.2910 (0.3); 3.8671 (1.1); 3.8563 (1.1); 3.8451 (0.3); 3.8288 (2.2); 3.8180 (2.0); 3.7649 (2.3); 3.7472 (2.1); 3.7264 (1.3); 3.7089 (1.1); 3.0508 (0.3); 3.0174 (0.4); 2.9948 (4.7); 2.9690 (3.2); 2.9227 (0.6); 2.8608 (0.8); 2.8530 (1.0); 2.8425 (5.2); 2.7206 (0.5); 2.6503 (2.0); 2.5976 (0.8); 2.5321 (0.8); 2.4973 (0.6); 2.4844 (0.6); 2.4606 (0.5); 2.4465 (1.0); 2.4387 (0.9); 2.4010 (16.0); 2.3710 (0.6); 2.3203 (1.3); 2.0073 (0.4); 1.8635 (0.6); 1.8469 (1.0); 1.8358 (1.0); 1.8191 (1.6); 1.8023 (1.0); 1.7911 (1.0); 1.7742 (0.5); 1.3947 (0.5); 1.3734 (0.5); 1.2921 (0.8); 0.9795 (1.3); 0.9648 (3.0); 0.9581 (3.4); 0.9439 (1.8); 0.9366 (3.2); 0.9299 (3.0); 0.9161 (1.4); 0.7074 (0.5); 0.6943 (0.7); 0.6880 (0.7); 0.6742 (1.6); 0.6597 (3.2); 0.6544 (2.9); 0.6431 (2.9); 0.6377 (3.1); 0.6219 (1.0); 0.1081 (2.7); 0.0485 (0.7); 0.0379 (24.0); 0.0270 (1.0) 4-13: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.3099 (0.4); 8.2680 (16.0); 8.1493 (2.0); 8.1212 (2.0); 8.0665 (0.7); 8.0229 (0.4); 7.8920 (0.4); 7.8079 (0.5); 7.7950 (0.6); 7.7795 (0.5); 7.7666 (0.3); 7.7239 (0.4); 7.7075 (0.6); 7.6898 (0.8); 7.6633 (7.2); 7.6458 (10.6); 7.6213 (0.4); 7.6091 (0.4); 7.5934 (0.6); 7.5833 (0.6); 7.5539 (0.7); 7.5422 (0.5); 7.4987 (4.9); 7.4689 (1.4); 7.4556 (2.4); 7.4458 (2.9); 7.4409 (3.5); 7.4343 (2.9); 7.4252 (2.4); 7.4171 (1.8); 7.3855 (0.5); 7.3574 (0.3); 7.2987 (31.6); 7.2496 (0.5); 7.2242 (0.5); 7.1890 (1.0); 7.1779 (6.1); 7.1515 (6.6); 7.1038 (0.7); 7.0909 (0.4); 7.0836 (0.4); 7.0653 (0.6); 7.0387 (0.6); 7.0150 (6.9); 7.0092 (6.9); 6.9476 (0.5); 6.9239 (0.5); 6.8969 (0.4); 6.8608 (3.9); 6.8549 (3.6); 6.8345 (3.3); 6.8286 (3.0); 5.6459 (0.4); 5.6374 (0.4); 5.5899 (0.4); 5.5433 (0.4); 5.5253 (0.4); 5.3373 (2.6); 4.8645 (0.4); 4.8525 (0.5); 4.8405 (1.0); 4.8286 (1.2); 4.8207 (1.4); 4.8094 (1.5); 4.7930 (1.3); 4.7810 (1.1); 4.7682 (0.6); 4.7566 (0.5); 4.3030 (0.6); 4.1825 (0.4); 4.1639 (0.4); 3.9301 (2.6); 3.9182 (2.6); 3.9087 (0.6); 3.8922 (4.4); 3.8805 (4.0); 3.8165 (0.4); 3.7884 (3.9); 3.7686 (3.9); 3.7505 (2.6); 3.7307 (2.5); 3.7018 (0.4); 3.1801 (0.5); 3.1540 (0.7); 3.1125 (7.9); 3.0882 (8.8); 3.0668 (0.7); 3.0438 (0.4); 3.0197 (0.3); 2.9948 (0.3); 2.8409 (4.2); 2.7308 (0.3); 2.6474 (0.7); 2.6029 (1.6); 2.5410 (1.6); 2.5226 (0.6); 2.5002 (0.6); 1.8814 (0.4); 1.8592 (1.0); 1.8425 (1.6); 1.8311 (1.9); 1.8143 (3.1); 1.7975 (1.9); 1.7865 (1.8); 1.7695 (0.9); 1.7490 (0.6); 1.7160 (0.5); 1.4777 (0.5); 1.4528 (1.1); 1.4360 (2.4); 1.4139 (2.4); 1.2912 (0.8); 1.0175 (2.2); 1.0021 (5.5); 0.9957 (6.3); 0.9807 (3.6); 0.9739 (6.0); 0.9677 (5.6); 0.9528 (2.8); 0.9344 (0.6); 0.9225 (0.5); 0.9025 (0.4); 0.7254 (0.7); 0.7083 (0.9); 0.6753 (2.8); 0.6599 (6.6); 0.6545 (5.7); 0.6434 (5.9); 0.6381 (6.8); 0.6219 (2.3); 0.1074 (3.3); 0.0477 (1.1); 0.0370 (40.0); 0.0261 (1.8) 4-14: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.2695 (5.8); 8.2625 (0.9); 8.1828 (0.8); 8.1548 (0.8); 7.6916 (0.4); 7.6631 (3.0); 7.6457 (4.2); 7.5532 (0.5); 7.5434 (0.4); 7.5142 (2.0); 7.4767 (0.4); 7.4648 (1.0); 7.4566 (1.0); 7.4500 (1.3); 7.4434 (1.2); 7.4345 (1.0); 7.4128 (0.4); 7.2989 (12.8); 7.2709 (0.4); 7.2285 (2.2); 7.2151 (0.5); 7.2021 (2.9); 7.1897 (2.8); 7.1842 (2.8); 7.0880 (0.4); 7.0270 (1.5); 7.0213 (1.4); 7.0008 (1.2); 6.9950 (1.1); 4.8509 (0.4); 4.8210 (0.6); 4.8040 (0.5); 4.7921 (0.4); 3.9394 (1.0); 3.9276 (1.0); 3.9016 (1.7); 3.8899 (1.6); 3.7964 (1.5); 3.7767 (1.4); 3.7585 (1.0); 3.7388 (1.0); 3.1540 (0.4); 3.1281 (2.5); 3.1056 (2.8); 3.0816 (0.4); 2.9943 (0.4); 2.8876 (0.4); 2.8645 (1.0); 2.8411 (4.0); 2.8185 (1.0); 2.7956 (0.5); 2.6492 (0.4); 2.6027 (0.8); 2.5422 (0.8); 1.4561 (0.5); 1.4389 (1.4); 1.4165 (1.4); 1.2823 (0.8); 1.2748 (0.7); 1.2586 (1.3); 1.2522 (0.8); 1.2427 (0.9); 1.2292 (16.0); 1.2062 (16.0); 1.1802 (0.8); 0.9339 (0.4); 0.1075 (1.1); 0.0371 (15.8); 0.0262 (0.9) 4-15: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.4712 (0.8); 8.4447 (0.8); 8.3224 (5.9); 7.6768 (0.3); 7.6632 (2.7); 7.6459 (3.9); 7.5189 (2.0); 7.4824 (0.5); 7.4673 (0.9); 7.4586 (0.8); 7.4525 (1.3); 7.4462 (1.1); 7.4368 (0.8); 7.4285 (0.7); 7.2988 (10.0); 7.1102 (1.8); 7.0843 (2.5); 7.0590 (0.4); 7.0294 (2.6); 6.9486 (1.4); 6.9434 (1.2); 6.9229 (1.0); 6.9176 (0.9); 5.3376 (1.4); 4.6526 (0.4); 4.6419 (0.5); 4.6355 (0.5); 4.6258 (0.6); 4.6141 (0.5); 4.6022 (0.5); 3.8770 (0.8); 3.8662 (0.8); 3.8387 (1.7); 3.8280 (1.5); 3.7791 (1.6); 3.7616 (1.5); 3.7407 (0.9); 3.7233 (0.8); 3.0131 (2.0); 3.0075 (2.2); 2.9911 (1.9); 2.9809 (1.8); 2.8848 (0.6); 2.8617 (1.4); 2.8420 (3.2); 2.8158 (1.1); 2.7931 (0.5); 2.7293 (0.4); 2.6419 (0.4); 2.5964 (0.7); 2.5343 (0.7); 2.4973 (0.5); 2.4886 (0.5); 2.4618 (0.6); 2.4321 (11.9); 2.3959 (0.8); 2.3282 (0.5); 1.4441 (0.7); 1.4222 (0.7); 1.2840 (1.1); 1.2753 (1.0); 1.2597 (2.0); 1.2419 (16.0); 1.2188 (15.5); 1.2028 (0.9); 1.1862 (0.6); 1.1793 (0.6); 0.1089 (1.1); 0.0383 (12.4); 0.0274 (0.6) 4-16: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.2731 (0.7); 8.2461 (0.7); 8.1328 (5.3); 7.2989 (11.8); 7.1537 (0.5); 7.1257 (1.7); 7.1141 (1.4); 7.1035 (4.1); 7.0926 (1.2); 7.0858 (1.4); 7.0658 (0.5); 7.0589 (0.4); 7.0230 (2.3); 7.0025 (0.8); 6.9766 (1.9); 6.9717 (1.7); 6.9543 (2.7); 6.9290 (0.8); 6.8727 (0.7); 6.8618 (0.7); 6.8510 (1.2); 6.8429 (1.0); 6.8254 (0.6); 6.8188 (0.6); 5.6229 (1.2); 5.3372 (2.5); 4.7436 (0.4); 4.7309 (0.5); 4.7218 (0.6); 4.7161 (0.5); 4.7091 (0.5); 4.7034 (0.5); 4.6943 (0.5); 4.6814 (0.4); 3.8777 (0.9); 3.8651 (0.9); 3.8399 (1.6); 3.8274 (1.5); 3.7492 (1.5); 3.7277 (1.4); 3.7115 (0.9); 3.6900 (0.8); 2.9940 (0.5); 2.9450 (3.2); 2.9223 (3.5); 2.8419 (9.9); 2.7348 (16.0); 2.2637 (0.4); 2.2083 (0.7); 2.1883 (10.9); 2.1765 (11.2); 2.1540 (0.7); 2.1368 (1.0); 2.1193 (0.6); 2.1087 (0.6); 1.7825 (0.6); 1.7429 (0.6); 1.6276 (0.4); 1.2936 (0.3); 1.0957 (0.7); 1.0813 (1.6); 1.0744 (1.9); 1.0679 (1.1); 1.0603 (1.2); 1.0526 (1.8); 1.0460 (1.8); 1.0321 (0.9); 0.8360 (0.9); 0.8217 (2.0); 0.8178 (2.0); 0.8046 (2.0); 0.8001 (2.0); 0.7835 (0.7); 0.1081 (2.6); 0.0492 (0.5); 0.0384 (14.4); 0.0275 (0.6) 4-17: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.4081 (1.0); 8.3812 (1.0); 8.3154 (9.0); 7.6623 (3.6); 7.6447 (5.2); 7.4867 (2.6); 7.4710 (0.4); 7.4574 (1.1); 7.4490 (0.9); 7.4426 (1.6); 7.4360 (1.2); 7.4272 (1.0); 7.4190 (0.6); 7.2983 (9.0); 7.0656 (2.4); 7.0401 (3.1); 6.9740 (2.9); 6.8883 (1.6); 6.8622 (1.2); 5.3371 (3.3); 4.6641 (0.6); 4.6534 (0.7); 4.6468 (0.8); 4.6371 (0.9); 4.6272 (0.7); 4.6208 (0.7); 4.6101 (0.6); 3.8790 (1.1); 3.8680 (1.2); 3.8407 (2.3); 3.8298 (2.1); 3.7752 (2.1); 3.7574 (2.1); 3.7369 (1.1); 3.7191 (1.1); 3.0029 (4.7); 2.9784 (4.6); 2.4252 (0.6); 2.3972 (16.0); 2.2980 (0.7); 2.2754 (14.8); 1.7687 (0.8); 1.6801 (0.7); 1.2936 (0.4); 0.0380 (8.2) 4-18: ¹H-NMR(400.2 MHz, d6-DMSO): δ = 8.6892 (3.3); 8.6678 (3.4); 8.0001 (16.0); 7.7646 (1.4); 7.7451 (4.1); 7.7255 (4.1); 7.7092 (4.9); 7.6895 (1.9); 7.6467 (5.6); 7.5657 (3.1); 7.5458 (2.5); 7.2498 (8.2); 7.2289 (10.6); 7.0991 (11.6); 7.0782 (8.9); 6.1717 (2.2); 5.7565 (8.3); 4.4375 (0.8); 4.4253 (1.1); 4.4151 (1.6); 4.4033 (1.6); 4.3937 (1.2); 4.3815 (0.8); 3.6291 (0.4); 3.6012 (7.2); 3.5860 (7.1); 3.5586 (0.3); 3.3272 (85.1); 2.9543 (1.7); 2.9424 (1.9); 2.9196 (2.4); 2.9079 (2.2); 2.7369 (2.3); 2.7143 (2.4); 2.7025 (1.9); 2.6796 (2.2); 2.6712 (1.5); 2.6667 (1.0); 2.5243 (6.3); 2.5107 (83.4); 2.5066 (162.9); 2.5022 (211.7); 2.4977 (157.3); 2.3334 (1.0); 2.3289 (1.4); 2.3245 (1.0); 2.0746 (5.0); 0.1461 (0.5); 0.0079 (4.9); −0.0002 (123.5); −0.1496 (0.6) 4-19: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.0332 (0.6); 7.5717 (0.4); 7.5459 (1.5); 7.5210 (3.9); 7.4956 (0.5); 7.4616 (2.2); 7.4198 (0.9); 7.4127 (1.5); 7.4057 (0.8); 7.3891 (0.9); 7.2988 (8.6); 7.1126 (1.9); 7.0870 (2.4); 6.9864 (2.4); 6.8986 (1.3); 6.8726 (1.1); 6.6832 (1.0); 6.6545 (1.0); 5.5815 (3.8); 5.3369 (1.1); 4.7528 (0.4); 4.7424 (0.5); 4.7341 (0.5); 4.7239 (0.7); 4.7137 (0.5); 4.7053 (0.5); 4.6958 (0.4); 3.8683 (0.9); 3.8572 (1.0); 3.8307 (1.7); 3.8197 (1.5); 3.7449 (1.5); 3.7256 (1.5); 3.7072 (0.9); 3.6881 (0.9); 2.9878 (5.0); 2.9601 (3.5); 2.9352 (3.4); 2.9113 (4.5); 2.6225 (15.1); 2.4649 (0.3); 2.4169 (0.4); 2.3932 (12.5); 2.3341 (0.4); 2.2726 (16.0); 2.2640 (12.5); 1.6449 (1.8); 0.0471 (0.4); 0.0363 (9.4); 0.0271 (0.3); 0.0255 (0.4) 4-20: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.4595 (0.7); 8.4329 (0.7); 8.1585 (5.2); 7.6163 (0.6); 7.5901 (1.6); 7.5641 (1.2); 7.4915 (1.4); 7.4659 (0.9); 7.3861 (1.8); 7.3698 (1.1); 7.3666 (1.2); 7.3432 (0.8); 7.3399 (0.9); 7.3361 (0.7); 7.2984 (10.5); 7.0769 (1.6); 7.0513 (2.1); 6.9720 (2.0); 6.9148 (1.1); 6.8908 (1.2); 6.8650 (0.9); 6.7270 (2.2); 6.5392 (1.1); 5.5669 (5.1); 5.3372 (0.5); 4.6689 (0.4); 4.6583 (0.4); 4.6516 (0.5); 4.6417 (0.6); 4.6314 (0.4); 4.6259 (0.4); 4.6144 (0.4); 4.1711 (0.6); 4.1473 (0.6); 3.8679 (0.8); 3.8566 (0.8); 3.8302 (1.6); 3.8190 (1.5); 3.7684 (1.5); 3.7504 (1.5); 3.7307 (0.8); 3.7127 (0.8); 2.9934 (3.3); 2.9690 (3.0); 2.8410 (2.3); 2.7424 (16.0); 2.4022 (11.2); 2.2764 (10.3); 2.0835 (2.6); 1.6153 (10.0); 1.3208 (0.7); 1.2971 (1.5); 1.2732 (0.7); 0.0479 (0.4); 0.0371 (10.9); 0.0262 (0.4) 4-21: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.3034 (1.9); 8.2740 (2.1); 8.2654 (16.0); 8.0558 (0.6); 7.7849 (0.3); 7.6968 (0.5); 7.6706 (4.5); 7.6623 (3.9); 7.6538 (8.8); 7.6508 (9.8); 7.5951 (0.6); 7.5866 (0.9); 7.5047 (10.8); 7.4984 (9.2); 7.4882 (1.2); 7.4743 (0.8); 7.4670 (1.0); 7.4533 (2.0); 7.4401 (2.7); 7.4335 (2.8); 7.4233 (2.1); 7.4146 (1.4); 7.3920 (0.4); 7.3849 (0.4); 7.3644 (0.4); 7.3315 (3.2); 7.3250 (3.1); 7.3040 (6.1); 7.2984 (31.9); 7.2753 (0.4); 7.2149 (7.8); 7.1875 (5.5); 7.1696 (0.4); 7.1567 (0.5); 5.5738 (6.6); 5.3366 (7.0); 4.8391 (0.4); 4.8280 (0.5); 4.8127 (1.0); 4.7985 (1.2); 4.7867 (1.5); 4.7769 (1.1); 4.7605 (1.0); 4.7446 (0.5); 4.7338 (0.4); 4.3157 (0.3); 3.9345 (0.4); 3.9210 (2.3); 3.9097 (2.6); 3.8969 (0.6); 3.8827 (4.3); 3.8715 (3.9); 3.8174 (0.4); 3.7966 (4.0); 3.7786 (4.0); 3.7582 (2.4); 3.7402 (2.2); 3.1939 (1.0); 3.1786 (0.6); 3.1676 (1.2); 3.1476 (4.3); 3.1224 (7.7); 3.1000 (4.2); 3.0769 (1.0); 3.0539 (0.9); 2.8451 (0.8); 2.6575 (0.4); 2.6119 (1.0); 2.5504 (0.8); 1.6958 (0.3); 1.6138 (6.2); 1.2931 (1.2); 0.1189 (0.4); 0.1070 (11.8); 0.0947 (0.4); 0.0477 (0.9); 0.0369 (27.1); 0.0259 (1.0) 4-22: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.6098 (1.1); 8.5848 (1.0); 8.3157 (7.9); 8.1002 (0.3); 7.6698 (2.3); 7.6647 (2.3); 7.6600 (2.3); 7.6522 (5.1); 7.6493 (5.4); 7.5979 (0.3); 7.5096 (2.6); 7.4825 (0.5); 7.4723 (0.5); 7.4575 (1.1); 7.4453 (1.5); 7.4385 (1.5); 7.4275 (1.3); 7.4188 (0.8); 7.3212 (3.1); 7.2987 (18.0); 7.2380 (1.4); 7.2324 (1.3); 7.2110 (1.9); 7.2047 (1.8); 7.1888 (0.3); 7.1625 (0.4); 7.0793 (3.5); 7.0522 (2.6); 5.5291 (5.3); 5.3371 (6.8); 4.5874 (0.6); 4.5768 (0.7); 4.5602 (0.8); 4.5505 (0.7); 4.5394 (0.6); 3.8568 (1.0); 3.8468 (1.2); 3.8338 (0.4); 3.8178 (2.2); 3.8079 (2.0); 3.7649 (0.3); 3.7487 (2.2); 3.7328 (2.1); 3.7099 (1.2); 3.6939 (1.1); 3.0645 (0.5); 3.0435 (0.7); 3.0189 (2.2); 2.9959 (3.6); 2.9664 (2.0); 2.9494 (0.6); 2.9206 (0.6); 2.4656 (0.6); 2.4346 (16.0); 2.4106 (0.4); 1.6023 (9.4); 1.2930 (0.7); 0.1074 (2.0); 0.0482 (0.6); 0.0375 (18.1) 4-23: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.7061 (3.1); 8.7000 (3.3); 8.5022 (3.0); 8.4943 (3.1); 8.3147 (7.1); 8.2932 (0.9); 8.2672 (1.0); 7.9204 (0.4); 7.9100 (0.4); 7.9021 (0.4); 7.8921 (0.6); 7.8128 (2.0); 7.8059 (3.2); 7.7985 (2.2); 7.7850 (0.6); 7.7774 (0.6); 7.7669 (0.6); 7.2989 (13.7); 7.0695 (2.0); 7.0440 (2.8); 6.9835 (2.7); 6.9132 (1.5); 6.8869 (1.1); 5.5729 (0.9); 5.3376 (16.0); 4.6530 (0.5); 4.6431 (0.6); 4.6369 (0.6); 4.6270 (0.8); 4.6179 (0.6); 4.6114 (0.6); 4.6013 (0.6); 3.8776 (0.9); 3.8669 (1.0); 3.8391 (2.0); 3.8284 (1.9); 3.7778 (1.8); 3.7604 (1.8); 3.7394 (1.0); 3.7220 (0.9); 3.0090 (4.1); 2.9845 (3.9); 2.4009 (13.8); 2.3299 (0.4); 2.3185 (0.8); 2.2940 (13.4); 2.2715 (0.9); 2.2568 (0.8); 1.6331 (0.3); 0.0480 (0.6); 0.0372 (17.0); 0.0263 (0.7) 4-24: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.5386 (0.4); 8.5271 (2.5); 8.5179 (2.5); 8.3170 (8.8); 8.2250 (1.2); 8.2127 (0.9); 8.1620 (0.9); 8.1354 (1.0); 7.9786 (3.0); 7.9694 (2.9); 7.9453 (0.4); 7.9353 (0.4); 7.9220 (0.3); 7.9118 (0.4); 7.8935 (0.5); 7.7965 (0.5); 7.7864 (0.3); 7.7783 (0.3); 7.7680 (0.3); 7.2990 (24.4); 7.1074 (0.4); 7.0909 (0.4); 7.0689 (2.2); 7.0434 (3.1); 7.0116 (0.6); 6.9805 (3.0); 6.9481 (0.4); 6.9109 (1.6); 6.8859 (1.2); 5.5826 (2.1); 5.3383 (10.8); 4.6635 (0.6); 4.6528 (0.7); 4.6466 (0.8); 4.6370 (0.9); 4.6270 (0.7); 4.6221 (0.7); 4.6107 (0.7); 3.8861 (1.0); 3.8754 (1.1); 3.8476 (2.3); 3.8370 (2.2); 3.8172 (0.4); 3.8045 (0.4); 3.7861 (2.2); 3.7686 (2.1); 3.7474 (1.4); 3.7301 (1.2); 3.0142 (4.5); 2.9896 (4.2); 2.9438 (0.5); 2.9207 (0.7); 2.4432 (0.4); 2.4011 (16.0); 2.3329 (0.7); 2.3103 (2.2); 2.2831 (14.0); 1.6055 (1.7); 1.3149 (0.8); 1.2940 (1.2); 0.1075 (0.4); 0.0484 (1.0); 0.0377 (29.5); 0.0268 (1.0) 4-25: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9196 (0.5); 7.9093 (0.5); 7.9016 (0.5); 7.8912 (0.8); 7.7948 (0.8); 7.7847 (0.6); 7.7767 (0.6); 7.7664 (0.5); 7.4570 (2.4); 7.4532 (2.4); 7.2988 (13.3); 7.2539 (0.4); 7.2258 (6.3); 7.2200 (3.2); 7.1925 (0.3); 7.1405 (0.7); 7.1147 (1.5); 7.0866 (1.4); 7.0690 (0.4); 7.0593 (1.0); 7.0530 (1.1); 7.0302 (1.2); 7.0085 (0.5); 7.0029 (0.5); 6.8549 (0.7); 6.8488 (0.8); 6.8281 (1.2); 6.8014 (1.5); 6.7719 (0.9); 5.6181 (4.4); 5.3376 (0.8); 4.8889 (0.3); 4.8788 (0.4); 4.8683 (0.5); 4.8582 (0.6); 4.8492 (0.6); 4.8395 (0.5); 4.8287 (0.4); 4.1784 (0.7); 3.9303 (0.9); 3.9190 (0.9); 3.8920 (1.6); 3.8808 (1.6); 3.7994 (1.4); 3.7799 (1.4); 3.7613 (0.9); 3.7418 (0.9); 3.1451 (0.4); 3.1167 (0.4); 3.0976 (1.8); 3.0834 (1.8); 3.0693 (2.1); 3.0617 (2.0); 2.8357 (0.8); 2.3794 (16.0); 2.3239 (1.1); 2.1326 (0.5); 2.1214 (0.5); 2.1044 (1.0); 2.0875 (0.6); 2.0766 (0.6); 1.5989 (5.9); 1.2920 (0.4); 1.0795 (0.6); 1.0656 (1.6); 1.0582 (1.9); 1.0443 (1.0); 1.0370 (1.7); 1.0298 (2.0); 1.0162 (0.8); 0.8242 (0.7); 0.8097 (2.1); 0.8043 (2.4); 0.7929 (2.1); 0.7868 (2.4); 0.7715 (0.7); 0.1071 (1.8); 0.0479 (0.6); 0.0372 (17.8); 0.0263 (0.7) 4-26: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9193 (0.5); 7.9089 (0.6); 7.9015 (0.5); 7.8909 (0.8); 7.7944 (0.8); 7.7844 (0.6); 7.7762 (0.6); 7.7659 (0.6); 7.2987 (12.3); 7.2294 (2.2); 7.2030 (2.5); 7.1225 (0.6); 7.0958 (1.7); 7.0689 (2.4); 7.0580 (1.5); 7.0423 (1.1); 7.0368 (1.4); 7.0215 (2.7); 7.0156 (3.2); 6.8431 (0.7); 6.8354 (0.8); 6.8144 (2.6); 6.7949 (0.8); 6.7884 (1.9); 6.7822 (1.3); 6.6886 (1.0); 6.6592 (1.0); 5.6212 (3.9); 4.8800 (0.3); 4.8690 (0.4); 4.8597 (0.4); 4.8491 (0.6); 4.8299 (0.4); 4.1775 (0.8); 3.9284 (0.9); 3.9168 (1.0); 3.8906 (1.6); 3.8791 (1.5); 3.7845 (1.4); 3.7640 (1.4); 3.7466 (0.9); 3.7263 (0.9); 3.0768 (2.1); 3.0724 (2.2); 3.0499 (3.3); 2.3638 (0.3); 2.3372 (16.0); 2.3249 (1.2); 2.1361 (0.5); 2.1256 (0.6); 2.1082 (1.0); 2.0911 (0.6); 2.0803 (0.6); 2.0439 (1.0); 1.8122 (0.4); 1.8014 (0.6); 1.7904 (0.6); 1.7734 (1.1); 1.7568 (0.6); 1.7455 (0.6); 1.6028 (5.1); 1.2914 (0.4); 1.0765 (0.6); 1.0617 (1.8); 1.0547 (2.1); 1.0405 (1.1); 1.0331 (2.0); 1.0264 (2.1); 1.0123 (0.9); 0.9830 (0.5); 0.9684 (1.6); 0.9624 (2.0); 0.9518 (1.0); 0.9403 (1.8); 0.9345 (1.8); 0.9235 (0.6); 0.9203 (0.7); 0.8168 (0.8); 0.8020 (2.2); 0.7968 (2.4); 0.7851 (2.2); 0.7795 (2.5); 0.7636 (0.8); 0.6314 (0.9); 0.6255 (0.9); 0.6162 (2.1); 0.6090 (1.8); 0.5999 (2.2); 0.5928 (1.1); 0.5837 (0.7); 0.1071 (6.3); 0.0481 (0.5); 0.0373 (16.0); 0.0264 (0.7) 4-27: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.5619 (1.0); 8.5346 (1.0); 8.2838 (8.1); 7.7928 (0.6); 7.7836 (0.5); 7.7744 (0.7); 7.7657 (0.3); 7.7025 (0.5); 7.6923 (0.4); 7.6843 (0.4); 7.6740 (0.3); 7.3996 (1.6); 7.3733 (3.5); 7.3469 (2.1); 7.2988 (6.2); 7.0700 (3.2); 7.0449 (3.8); 7.0160 (0.4); 6.9932 (1.8); 6.9843 (3.4); 6.9767 (3.7); 6.9611 (2.0); 6.9587 (1.9); 6.9248 (2.3); 6.9187 (3.1); 6.9121 (1.9); 6.8917 (1.8); 6.8664 (1.4); 4.6466 (0.6); 4.6360 (0.6); 4.6293 (0.7); 4.6192 (0.9); 4.6097 (0.7); 4.6031 (0.7); 4.5922 (0.6); 4.1949 (0.6); 4.1711 (1.7); 4.1473 (1.6); 4.1233 (0.6); 3.8587 (1.1); 3.8477 (1.2); 3.8207 (2.2); 3.8097 (2.2); 3.7581 (2.2); 3.7401 (2.1); 3.7202 (1.2); 3.7022 (1.1); 2.9941 (1.4); 2.9830 (4.7); 2.9585 (4.6); 2.9196 (1.2); 2.8414 (6.7); 2.7765 (0.7); 2.7476 (0.5); 2.5799 (4.9); 2.4403 (0.4); 2.4167 (0.4); 2.4004 (16.0); 2.3736 (2.3); 2.3263 (0.7); 2.3142 (1.4); 2.3081 (1.3); 2.2866 (15.0); 2.2395 (1.7); 2.0831 (6.8); 2.0120 (0.4); 2.0035 (0.6); 1.9950 (0.8); 1.9838 (0.8); 1.9670 (1.6); 1.9504 (0.9); 1.9391 (0.9); 1.9223 (0.5); 1.5055 (0.5); 1.4812 (1.7); 1.4591 (1.5); 1.3211 (1.8); 1.2973 (3.7); 1.2735 (1.8); 1.0862 (0.9); 1.0709 (2.4); 1.0643 (2.7); 1.0496 (1.4); 1.0427 (2.7); 1.0363 (2.6); 1.0216 (1.3); 0.7921 (1.1); 0.7767 (3.1); 0.7710 (2.9); 0.7605 (2.7); 0.7548 (3.4); 0.7387 (1.1); 0.1102 (0.5); 0.0385 (7.4) 4-28: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.2998 (1.3); 7.4893 (0.4); 7.2986 (8.8); 7.2093 (0.4); 7.2028 (0.4); 7.1543 (0.4); 7.1462 (0.5); 7.1265 (0.3); 7.1187 (0.5); 7.0742 (0.4); 7.0487 (0.5); 6.9802 (0.5); 5.5613 (1.1); 3.8287 (0.4); 3.8178 (0.3); 3.7662 (0.4); 3.7485 (0.3); 2.9941 (0.7); 2.9695 (0.7); 2.4038 (2.5); 2.2835 (2.2); 1.6232 (0.4); 1.6179 (0.5); 1.6126 (0.4); 1.5880 (16.0); 1.5590 (0.4); 1.5544 (0.4); 1.2979 (0.5); 1.1756 (0.4); 1.1698 (0.4); 1.1460 (0.4); 1.1411 (0.3); 0.9201 (0.4); 0.0488 (0.6); 0.0380 (10.3); 0.0270 (0.4) 4-29: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.2419 (0.7); 8.2122 (0.8); 8.0974 (5.3); 8.0861 (0.4); 7.8929 (0.4); 7.7941 (0.4); 7.7760 (0.3); 7.2989 (13.3); 7.1923 (2.2); 7.1661 (2.6); 7.1436 (3.1); 7.1315 (1.8); 7.1281 (1.8); 7.1243 (2.1); 7.1188 (2.7); 7.1013 (0.4); 7.0417 (2.4); 7.0357 (2.6); 6.8800 (0.7); 6.8672 (0.6); 6.8591 (1.1); 6.8478 (1.2); 6.8356 (0.6); 6.8269 (1.9); 6.8213 (1.5); 6.8009 (1.3); 6.7949 (1.2); 5.6215 (1.3); 5.3370 (4.1); 4.8519 (0.4); 4.8295 (0.5); 4.8247 (0.5); 4.8173 (0.5); 4.8031 (0.4); 4.7917 (0.4); 3.9274 (0.9); 3.9151 (1.0); 3.8899 (1.6); 3.8775 (1.4); 3.7826 (1.4); 3.7619 (1.4); 3.7450 (1.0); 3.7244 (0.9); 3.1532 (0.3); 3.1079 (1.8); 3.0969 (1.8); 3.0858 (1.8); 3.0715 (1.6); 2.8410 (4.4); 2.7235 (16.0); 2.5966 (0.4); 2.1746 (0.5); 2.1637 (0.5); 2.1463 (1.0); 2.1290 (0.6); 2.1182 (0.6); 1.8443 (0.6); 1.8332 (0.6); 1.8164 (1.1); 1.7996 (0.6); 1.7887 (0.6); 1.7716 (0.3); 1.6153 (1.6); 1.0977 (0.6); 1.0825 (1.8); 1.0758 (2.0); 1.0611 (1.1); 1.0540 (2.0); 1.0474 (2.0); 1.0329 (1.0); 0.9983 (0.7); 0.9833 (1.9); 0.9768 (2.0); 0.9623 (0.9); 0.9551 (2.0); 0.9486 (1.8); 0.9344 (0.8); 0.8414 (0.9); 0.8264 (2.1); 0.8205 (2.2); 0.8096 (2.0); 0.8036 (2.4); 0.7875 (0.8); 0.6747 (0.9); 0.6597 (2.1); 0.6535 (1.8); 0.6433 (2.0); 0.6381 (2.1); 0.6220 (0.8); 0.1077 (0.7); 0.0486 (0.5); 0.0377 (16.6); 0.0267 (0.6) 4-30: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.3096 (5.0); 7.2989 (16.5); 7.2825 (2.6); 7.1373 (0.5); 7.1340 (0.5); 7.1103 (1.4); 7.0917 (1.8); 7.0845 (2.6); 7.0642 (1.5); 7.0574 (1.8); 7.0530 (1.3); 7.0353 (1.0); 7.0299 (1.2); 7.0085 (0.5); 7.0028 (0.4); 6.8553 (0.7); 6.8489 (0.7); 6.8287 (1.1); 6.8067 (0.7); 6.8012 (0.7); 6.7892 (0.8); 6.7592 (0.8); 5.6176 (3.0); 5.3374 (12.2); 4.8777 (0.4); 4.8697 (0.4); 4.8602 (0.5); 4.8501 (0.5); 4.8402 (0.4); 4.8286 (0.4); 4.1028 (0.4); 3.9329 (0.9); 3.9216 (0.9); 3.8948 (1.5); 3.8835 (1.4); 3.8026 (1.4); 3.7831 (1.4); 3.7646 (0.9); 3.7451 (0.8); 3.1123 (1.7); 3.0995 (1.6); 3.0842 (1.9); 3.0775 (1.9); 2.3821 (16.0); 2.2885 (0.4); 2.1316 (0.4); 2.1204 (0.5); 2.1034 (0.9); 2.0822 (0.7); 2.0751 (0.5); 1.5982 (6.8); 1.2964 (0.6); 1.2918 (0.6); 1.0792 (0.6); 1.0654 (1.5); 1.0579 (1.8); 1.0438 (1.0); 1.0367 (1.5); 1.0296 (1.7); 1.0156 (0.8); 0.8232 (0.7); 0.8089 (1.9); 0.8028 (2.1); 0.7918 (1.9); 0.7856 (2.1); 0.7704 (0.7); 0.1074 (7.8); 0.0488 (0.6); 0.0379 (18.2); 0.0270 (0.7) 4-31: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.4207 (0.4); 8.3917 (0.4); 8.2335 (3.6); 7.4023 (0.8); 7.3760 (1.6); 7.3621 (1.8); 7.3551 (1.8); 7.3499 (1.1); 7.2986 (4.6); 7.2540 (1.2); 7.2264 (1.8); 7.1469 (1.2); 7.1399 (1.1); 7.1195 (0.7); 7.1125 (0.6); 7.0670 (0.9); 7.0409 (0.7); 6.9860 (0.6); 6.9833 (0.6); 6.9781 (0.8); 6.9593 (0.5); 6.9565 (0.5); 6.9513 (0.7); 6.9487 (0.6); 6.9156 (1.0); 6.9096 (1.3); 6.9030 (0.7); 4.7806 (0.4); 4.1917 (1.2); 4.1678 (3.5); 4.1440 (3.6); 4.1203 (1.2); 3.9080 (0.5); 3.8964 (0.6); 3.8699 (0.9); 3.8584 (0.9); 3.7813 (0.9); 3.7626 (1.0); 3.7429 (0.7); 3.7244 (0.5); 3.1204 (2.2); 3.0960 (2.1); 2.9933 (1.2); 2.9180 (1.0); 2.8382 (6.0); 2.7013 (1.4); 2.0802 (16.0); 1.9951 (0.4); 1.9839 (0.4); 1.9722 (0.5); 1.9673 (0.8); 1.9503 (0.5); 1.9392 (0.5); 1.7230 (0.6); 1.7108 (0.6); 1.5112 (0.7); 1.4863 (0.8); 1.4791 (0.6); 1.3178 (4.1); 1.2940 (8.4); 1.2701 (4.1); 1.0869 (0.4); 1.0716 (1.0); 1.0649 (1.2); 1.0500 (0.7); 1.0433 (1.2); 1.0369 (1.2); 1.0220 (0.6); 0.7904 (0.5); 0.7750 (1.4); 0.7693 (1.2); 0.7588 (1.2); 0.7530 (1.6); 0.7367 (0.5); 0.1050 (0.8); 0.0342 (4.5) 4-32: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.5021 (0.6); 8.4782 (0.7); 8.4594 (0.6); 8.2996 (8.4); 7.2986 (26.2); 7.2793 (1.0); 7.2719 (2.0); 7.2658 (3.1); 7.2600 (2.0); 7.2515 (1.6); 7.2470 (3.1); 7.2421 (2.7); 7.2206 (0.7); 7.2153 (0.6); 7.1960 (1.0); 7.1802 (1.0); 7.1659 (0.9); 7.1506 (0.4); 7.0859 (1.5); 7.0608 (1.9); 6.9723 (2.0); 6.8936 (1.5); 6.8690 (1.2); 5.5708 (3.8); 5.5626 (3.6); 4.6565 (0.4); 4.6463 (0.6); 4.6290 (0.7); 4.6207 (0.7); 4.6123 (0.6); 4.6051 (0.6); 4.1959 (1.2); 4.1721 (3.6); 4.1482 (3.5); 4.1244 (1.2); 3.8721 (0.9); 3.8615 (1.0); 3.8339 (2.0); 3.8231 (1.8); 3.7708 (1.6); 3.7534 (1.5); 3.7314 (0.8); 3.7132 (0.7); 3.0096 (4.0); 2.9856 (3.4); 2.9618 (0.4); 2.9203 (0.7); 2.8903 (0.7); 2.8509 (0.4); 2.4095 (10.9); 2.2747 (7.4); 2.2666 (7.6); 2.0839 (16.0); 2.0469 (0.5); 2.0295 (0.5); 2.0200 (0.6); 2.0074 (0.9); 2.0028 (0.7); 1.9901 (0.8); 1.9807 (1.0); 1.9681 (0.6); 1.9633 (1.0); 1.9507 (0.5); 1.9415 (0.5); 1.9241 (0.5); 1.7924 (0.3); 1.7752 (0.3); 1.7613 (0.6); 1.7485 (0.8); 1.7375 (0.6); 1.7341 (0.6); 1.7229 (0.8); 1.7103 (0.6); 1.7063 (0.6); 1.5885 (8.1); 1.3676 (0.4); 1.3453 (0.8); 1.3217 (5.6); 1.2980 (12.7); 1.2741 (4.6); 0.9420 (1.9); 0.9202 (6.1); 0.8971 (2.2); 0.0489 (1.3); 0.0381 (35.2); 0.0272 (1.5) 4-33: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.5286 (0.7); 8.5005 (0.7); 8.2051 (5.0); 7.9219 (0.4); 7.9115 (0.4); 7.9037 (0.4); 7.8935 (0.5); 7.7953 (0.5); 7.7853 (0.4); 7.7772 (0.4); 7.7669 (0.4); 7.5796 (3.1); 7.5762 (3.6); 7.5670 (1.5); 7.5562 (1.9); 7.5298 (0.5); 7.4890 (1.8); 7.4218 (0.8); 7.4144 (1.0); 7.3996 (0.9); 7.3924 (1.0); 7.3835 (0.5); 7.2985 (15.9); 6.9612 (0.9); 6.9339 (1.1); 6.8975 (1.8); 6.7512 (2.2); 6.7237 (1.7); 5.6826 (3.0); 5.3377 (8.4); 4.9848 (0.3); 4.9715 (0.6); 4.9587 (0.6); 4.9464 (0.6); 4.9342 (0.5); 4.9197 (0.4); 4.2084 (3.1); 4.1955 (3.7); 4.1060 (0.8); 4.0822 (0.8); 4.0678 (1.7); 4.0440 (1.6); 4.0116 (1.6); 3.9964 (1.6); 3.9734 (0.8); 3.9582 (0.7); 2.7713 (16.0); 2.3256 (0.7); 2.2648 (10.3); 2.2413 (0.4); 2.1848 (0.4); 1.9744 (10.4); 1.6013 (2.6); 0.1075 (0.8); 0.0486 (0.8); 0.0378 (19.7); 0.0268 (0.7) 4-34: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.6187 (0.7); 8.5920 (0.7); 8.1920 (5.3); 7.9206 (0.3); 7.9103 (0.4); 7.8922 (0.5); 7.7945 (0.5); 7.7848 (0.3); 7.7763 (0.4); 7.7660 (0.4); 7.6089 (3.3); 7.6055 (3.0); 7.5969 (1.5); 7.5920 (2.2); 7.5888 (2.1); 7.5203 (1.7); 7.4600 (0.8); 7.4504 (0.8); 7.4460 (0.5); 7.4403 (1.0); 7.4337 (0.8); 7.4293 (0.6); 7.4211 (0.4); 7.2985 (12.5); 7.2341 (0.4); 7.2226 (4.1); 7.2152 (1.3); 7.2000 (1.4); 7.1925 (4.6); 7.1812 (0.4); 6.7972 (0.5); 6.7857 (4.7); 6.7782 (1.4); 6.7631 (1.3); 6.7556 (4.0); 6.7441 (0.4); 5.6493 (3.9); 5.3370 (4.7); 4.8959 (0.4); 4.8903 (0.5); 4.8837 (0.5); 4.8789 (0.5); 4.8691 (0.5); 4.8626 (0.5); 4.8578 (0.4); 4.2576 (0.6); 4.2468 (0.7); 4.2262 (1.8); 4.2155 (1.6); 4.1973 (1.8); 4.1796 (2.0); 4.1659 (0.7); 4.1480 (0.7); 4.0809 (0.8); 4.0590 (0.7); 4.0424 (1.7); 4.0206 (1.6); 3.9863 (1.6); 3.9711 (1.7); 3.9479 (0.8); 3.9327 (0.7); 2.7754 (16.0); 1.6059 (2.7); 0.1068 (0.6); 0.0476 (0.6); 0.0368 (15.6); 0.0259 (0.5) 4-35: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.6003 (0.9); 8.5741 (0.9); 8.3001 (8.1); 7.6370 (3.8); 7.6197 (4.9); 7.5115 (2.4); 7.4735 (1.0); 7.4652 (0.9); 7.4579 (1.4); 7.4516 (1.2); 7.4430 (0.8); 7.4348 (0.6); 7.3728 (2.2); 7.3471 (2.5); 7.2991 (8.9); 6.9878 (5.4); 6.9615 (1.4); 5.5215 (3.5); 5.3380 (12.9); 4.6777 (0.4); 4.6665 (0.5); 4.6542 (0.7); 4.6408 (0.7); 4.6342 (0.7); 4.6274 (0.5); 4.6163 (0.4); 4.0228 (1.3); 4.0038 (1.2); 3.9842 (2.0); 3.9653 (1.9); 3.8697 (2.0); 3.8573 (1.9); 3.8311 (1.3); 3.8188 (1.2); 3.3324 (0.8); 3.3156 (0.8); 3.2865 (2.2); 3.2697 (2.1); 3.2431 (2.3); 3.2199 (2.3); 3.1972 (1.0); 3.1740 (0.8); 2.4148 (0.5); 2.3205 (16.0); 2.2827 (15.2); 1.6218 (0.5); 0.1081 (0.8); 0.0486 (0.4); 0.0377 (10.5); 0.0269 (0.4) 4-36: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.2983 (3.2); 7.2436 (0.4); 7.2238 (0.9); 7.2170 (0.9); 7.2036 (2.7); 7.2000 (2.1); 7.1941 (2.4); 7.1793 (2.9); 7.1761 (2.7); 7.1522 (0.8); 7.1222 (1.2); 7.1022 (2.3); 7.0889 (2.0); 7.0770 (1.9); 7.0633 (1.5); 7.0413 (0.8); 7.0131 (0.7); 6.9793 (1.6); 6.9559 (2.0); 6.9286 (0.7); 6.8896 (0.9); 6.8630 (0.8); 6.8475 (0.8); 6.8206 (0.6); 5.5829 (1.2); 4.7230 (0.5); 4.7118 (0.6); 4.7053 (0.7); 4.6948 (0.7); 4.6871 (0.6); 4.6766 (0.6); 4.1846 (0.5); 4.1608 (1.7); 4.1369 (1.7); 4.1132 (0.6); 3.8525 (0.6); 3.8453 (0.7); 3.8420 (0.8); 3.8352 (0.6); 3.8145 (1.1); 3.8075 (1.4); 3.7974 (1.1); 3.7377 (0.9); 3.7258 (1.0); 3.7196 (1.1); 3.7064 (0.9); 3.6999 (0.7); 3.6879 (0.6); 3.6816 (0.6); 3.6685 (0.5); 2.9586 (2.2); 2.9468 (2.3); 2.9336 (2.3); 2.9221 (2.1); 2.8998 (0.4); 2.8810 (0.4); 2.8694 (0.8); 2.8597 (0.6); 2.8396 (0.6); 2.8299 (0.8); 2.8186 (0.4); 2.8001 (0.4); 2.7910 (0.3); 2.4134 (1.0); 2.3959 (7.9); 2.3816 (16.0); 2.3425 (10.1); 2.3296 (1.1); 2.2935 (0.6); 2.2831 (0.6); 2.2588 (6.9); 2.2246 (6.5); 2.0752 (7.7); 1.9970 (0.4); 1.9798 (0.4); 1.9703 (0.5); 1.9572 (0.9); 1.9537 (0.7); 1.9403 (0.8); 1.9308 (0.9); 1.9138 (1.0); 1.9009 (0.5); 1.8915 (0.5); 1.8742 (0.4); 1.7434 (0.6); 1.7298 (0.8); 1.7162 (1.1); 1.7022 (1.1); 1.6882 (1.0); 1.6745 (1.0); 1.6608 (0.7); 1.6473 (0.4); 1.3166 (2.2); 1.2928 (4.4); 1.2690 (2.1); 0.0382 (3.3) 4-37: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.2876 (0.6); 8.2607 (0.6); 8.1486 (5.1); 7.6268 (0.6); 7.6044 (1.5); 7.5780 (1.6); 7.5535 (0.7); 7.4033 (0.8); 7.3759 (1.2); 7.3496 (0.5); 7.2985 (4.2); 7.0874 (1.6); 7.0618 (2.0); 6.9601 (1.9); 6.8875 (1.1); 6.8621 (0.8); 5.5849 (1.6); 5.3350 (12.2); 4.6868 (0.3); 4.6755 (0.4); 4.6685 (0.4); 4.6589 (0.5); 4.6492 (0.4); 4.6424 (0.4); 4.6311 (0.4); 4.1708 (0.6); 4.1470 (0.6); 3.8762 (0.7); 3.8647 (0.8); 3.8385 (1.6); 3.8271 (1.4); 3.7780 (1.4); 3.7595 (1.4); 3.7402 (0.7); 3.7218 (0.7); 3.0075 (3.2); 2.9833 (3.0); 2.7472 (16.0); 2.4296 (0.8); 2.4052 (10.6); 2.2830 (0.7); 2.2552 (9.7); 2.0817 (2.8); 1.7931 (1.0); 1.7119 (1.0); 1.3202 (0.7); 1.2964 (1.5); 1.2726 (0.7); 0.0379 (5.2) 4-38: ¹H-NMR(300.2 MHz, d6-DMSO): δ = 8.7017 (1.5); 8.6718 (1.5); 7.8368 (1.3); 7.7887 (0.7); 7.7665 (1.9); 7.7400 (2.2); 7.7098 (7.4); 7.5775 (1.1); 7.5505 (1.6); 7.5231 (0.7); 7.4864 (3.3); 7.4792 (3.5); 7.3898 (2.5); 7.3622 (3.1); 7.1153 (1.8); 7.1081 (1.8); 7.0878 (1.5); 7.0806 (1.5); 6.1721 (1.7); 5.7775 (14.2); 4.6318 (0.5); 4.6126 (0.6); 4.6007 (0.6); 4.5819 (0.5); 3.7275 (0.3); 3.7071 (0.4); 3.6918 (1.9); 3.6819 (2.0); 3.6715 (2.0); 3.6621 (1.9); 3.6465 (0.4); 3.6269 (0.3); 3.3477 (16.0); 3.1251 (0.8); 3.1110 (0.8); 3.0785 (1.1); 3.0646 (1.0); 2.8723 (1.0); 2.8378 (1.0); 2.8254 (0.8); 2.7915 (0.7); 2.7580 (0.5); 2.7369 (0.5); 2.7103 (0.8); 2.6054 (15.8); 2.5479 (0.6); 2.5348 (3.7); 2.5287 (8.0); 2.5227 (10.9); 2.5166 (7.9); 2.5107 (3.8); 2.4635 (2.1); 2.3667 (1.8); 0.0206 (8.2) 4-39: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.3324 (0.7); 8.3049 (0.7); 8.1039 (5.2); 7.6217 (0.6); 7.5960 (1.6); 7.5695 (1.2); 7.4957 (1.4); 7.4699 (0.9); 7.3878 (1.8); 7.3639 (1.3); 7.3600 (1.2); 7.3527 (3.0); 7.3456 (3.0); 7.3374 (1.1); 7.2988 (11.9); 7.2668 (1.9); 7.2394 (3.0); 7.1571 (1.9); 7.1500 (1.8); 7.1296 (1.2); 7.1226 (1.1); 6.9191 (1.1); 6.7312 (2.2); 6.5435 (1.1); 5.5799 (2.6); 5.3368 (3.7); 4.8289 (0.4); 4.8178 (0.4); 4.8112 (0.5); 4.8000 (0.6); 4.7895 (0.5); 4.7832 (0.4); 4.7718 (0.4); 3.9172 (0.9); 3.9055 (0.9); 3.8795 (1.6); 3.8678 (1.6); 3.7948 (1.5); 3.7764 (1.5); 3.7570 (0.9); 3.7387 (0.9); 3.1338 (3.3); 3.1093 (3.5); 2.8453 (0.6); 2.8403 (0.6); 2.8350 (0.3); 2.7397 (16.0); 2.6125 (1.5); 2.5495 (1.4); 2.5157 (0.4); 1.6176 (1.8); 0.1069 (1.4); 0.0479 (0.4); 0.0370 (13.9); 0.0262 (0.6) 4-40: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.4530 (0.6); 8.4252 (0.6); 8.2973 (5.7); 7.5343 (0.5); 7.5289 (0.4); 7.5193 (0.9); 7.5104 (1.0); 7.5046 (0.8); 7.4916 (0.6); 7.4868 (0.6); 7.4825 (0.5); 7.3646 (0.4); 7.3412 (1.0); 7.3220 (1.2); 7.3154 (2.6); 7.2989 (17.2); 7.2638 (0.5); 7.0842 (1.5); 7.0586 (2.0); 6.9716 (1.9); 6.8960 (1.1); 6.8709 (0.8); 5.6073 (0.4); 5.5762 (5.0); 4.6576 (0.4); 4.6469 (0.4); 4.6404 (0.5); 4.6310 (0.6); 4.6212 (0.5); 4.6145 (0.5); 4.6042 (0.4); 4.1722 (0.9); 4.1484 (0.9); 3.8721 (0.7); 3.8612 (0.8); 3.8340 (1.6); 3.8230 (1.5); 3.7709 (1.5); 3.7530 (1.5); 3.7328 (0.8); 3.7147 (0.7); 3.0064 (3.1); 2.9822 (2.9); 2.4415 (0.9); 2.4075 (10.4); 2.3358 (0.8); 2.2694 (9.7); 2.0843 (3.9); 1.5935 (16.0); 1.5570 (0.4); 1.5308 (1.4); 1.5080 (0.6); 1.4945 (0.5); 1.4714 (1.2); 1.4674 (1.3); 1.4452 (0.6); 1.3450 (0.4); 1.3219 (1.5); 1.2982 (3.6); 1.2744 (1.2); 1.2454 (0.6); 1.2234 (1.5); 1.2164 (1.6); 1.1938 (1.7); 1.1868 (1.3); 1.1668 (0.4); 0.9421 (0.7); 0.9203 (2.1); 0.8970 (0.8); 0.0491 (0.7); 0.0382 (21.3); 0.0273 (0.9) 4-41: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.8732 (1.6); 7.8631 (1.6); 7.8615 (1.5); 7.8569 (1.5); 7.8526 (2.0); 7.8441 (4.0); 7.8311 (2.2); 7.8184 (4.0); 7.8096 (1.8); 7.8054 (1.5); 7.8007 (1.6); 7.7890 (1.6); 7.5862 (1.0); 7.5588 (1.0); 7.4160 (0.4); 7.4110 (0.6); 7.4061 (0.4); 7.3897 (1.0); 7.3849 (1.0); 7.3686 (0.5); 7.3641 (0.7); 7.3590 (0.5); 7.3304 (0.5); 7.3255 (0.4); 7.2988 (15.8); 7.2835 (0.7); 7.2802 (0.8); 7.2504 (1.7); 7.2249 (1.9); 7.1945 (1.0); 7.1679 (1.3); 7.1416 (0.5); 7.0038 (1.9); 6.9642 (1.1); 6.9388 (0.9); 4.6866 (0.6); 4.6756 (0.5); 4.6623 (0.6); 4.6512 (0.4); 4.6163 (1.2); 4.6052 (0.8); 4.5824 (1.2); 4.5713 (1.0); 4.2033 (1.0); 4.1934 (1.1); 4.1699 (1.0); 4.1596 (0.9); 3.3053 (0.5); 3.2821 (0.5); 3.2589 (0.9); 3.2352 (0.9); 3.1605 (0.9); 3.1323 (0.9); 3.1142 (0.6); 3.0859 (0.5); 2.9939 (0.3); 2.8404 (6.7); 2.4840 (0.5); 2.4542 (10.0); 2.4112 (15.0); 2.3531 (0.4); 2.3131 (0.6); 2.2740 (9.4); 2.0836 (0.5); 1.6095 (16.0); 1.4447 (0.4); 1.4224 (1.2); 1.4187 (1.3); 1.3963 (0.6); 1.3818 (0.4); 1.3595 (1.2); 1.3554 (1.3); 1.3333 (0.6); 1.2975 (0.6); 1.1599 (0.5); 1.1380 (1.4); 1.1308 (1.6); 1.1083 (1.6); 1.1009 (1.2); 1.0814 (0.4); 0.9197 (0.5); 0.0486 (0.6); 0.0378 (18.9); 0.0268 (0.8) 4-42: ¹HNMR(300.2 MHz, CDCl3): δ = 8.1022 (5.4); 8.0922 (1.3); 8.0640 (0.8); 7.8915 (0.3); 7.7933 (0.3); 7.4291 (0.7); 7.4231 (0.8); 7.4076 (0.8); 7.4022 (1.4); 7.3966 (1.1); 7.3821 (0.8); 7.3751 (0.9); 7.2989 (8.7); 7.2812 (0.5); 7.2745 (1.6); 7.2685 (1.0); 7.2539 (1.4); 7.2469 (1.1); 7.2353 (1.7); 7.2317 (1.5); 7.2095 (1.4); 7.2047 (1.6); 7.1856 (2.4); 7.1773 (0.9); 7.1595 (2.6); 7.0244 (2.4); 7.0186 (2.6); 6.8480 (1.4); 6.8421 (1.4); 6.8217 (1.2); 6.8159 (1.2); 5.6152 (0.6); 5.3363 (0.4); 4.8492 (0.4); 4.8370 (0.4); 4.8279 (0.5); 4.8158 (0.5); 4.8006 (0.4); 4.7885 (0.4); 3.9276 (0.9); 3.9152 (1.0); 3.8900 (1.6); 3.8777 (1.4); 3.7879 (1.4); 3.7683 (1.7); 3.7503 (0.9); 3.7299 (0.9); 3.1079 (3.5); 3.0837 (2.9); 2.8403 (2.4); 2.7314 (16.0); 1.8440 (0.6); 1.8326 (0.6); 1.8161 (1.2); 1.7996 (0.7); 1.7882 (0.7); 1.7713 (0.4); 1.6558 (0.5); 1.2920 (0.4); 1.0066 (0.7); 0.9913 (1.9); 0.9847 (2.1); 0.9697 (1.1); 0.9630 (2.0); 0.9567 (1.9); 0.9419 (0.9); 0.6788 (0.9); 0.6635 (2.4); 0.6581 (2.1); 0.6470 (2.0); 0.6415 (2.5); 0.6253 (0.8); 0.1074 (1.8); 0.0478 (0.3); 0.0370 (11.4); 0.0262 (0.5) 4-43: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.3602 (0.6); 8.3335 (0.6); 8.1421 (5.1); 7.4271 (0.7); 7.4209 (0.8); 7.4056 (0.7); 7.4005 (1.1); 7.3980 (1.0); 7.3945 (1.0); 7.3807 (0.8); 7.3730 (0.9); 7.2988 (8.8); 7.2906 (0.6); 7.2840 (0.6); 7.2703 (0.4); 7.2628 (1.6); 7.2566 (1.0); 7.2429 (1.4); 7.2350 (1.3); 7.2312 (1.8); 7.2281 (1.5); 7.2061 (1.2); 7.2014 (1.4); 7.1787 (0.4); 7.1739 (0.5); 7.0840 (1.7); 7.0579 (2.0); 6.8671 (1.9); 6.7738 (1.1); 6.7680 (1.0); 6.7478 (0.9); 6.7417 (0.8); 5.5789 (1.3); 4.6600 (0.4); 4.6490 (0.4); 4.6420 (0.4); 4.6337 (0.5); 4.6077 (0.3); 4.1713 (0.5); 4.1474 (0.5); 3.8635 (0.7); 3.8521 (0.8); 3.8256 (1.5); 3.8143 (1.4); 3.7618 (1.4); 3.7434 (1.4); 3.7240 (0.8); 3.7056 (0.7); 2.9935 (2.6); 2.9718 (1.8); 2.9667 (1.8); 2.8411 (1.0); 2.7429 (16.0); 2.7301 (0.7); 2.4580 (0.6); 2.4374 (0.4); 2.4081 (10.7); 2.0833 (2.4); 1.8413 (0.5); 1.8301 (0.5); 1.8132 (1.0); 1.7964 (0.6); 1.7854 (0.6); 1.6250 (0.8); 1.3209 (0.6); 1.2971 (1.3); 1.2733 (0.6); 0.9681 (0.7); 0.9537 (1.8); 0.9467 (2.0); 0.9402 (1.0); 0.9325 (1.1); 0.9252 (1.9); 0.9186 (1.7); 0.9045 (0.9); 0.6718 (0.9); 0.6574 (2.1); 0.6547 (1.8); 0.6511 (1.8); 0.6406 (1.9); 0.6354 (2.0); 0.6193 (0.7); 0.1079 (0.7); 0.0482 (0.3); 0.0375 (11.6); 0.0298 (0.4); 0.0282 (0.3); 0.0266 (0.4) 4-44: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.4905 (0.7); 8.4635 (0.7); 8.1392 (0.7); 8.1295 (5.1); 7.4299 (0.7); 7.4237 (0.8); 7.4082 (0.8); 7.4032 (1.2); 7.4006 (1.2); 7.3974 (1.1); 7.3833 (0.8); 7.3756 (0.9); 7.3140 (2.0); 7.3082 (2.4); 7.2989 (11.8); 7.2725 (1.7); 7.2664 (1.1); 7.2526 (1.6); 7.2447 (1.4); 7.2402 (2.0); 7.2370 (1.9); 7.2262 (1.0); 7.2151 (1.4); 7.2102 (2.0); 7.2063 (1.8); 7.1989 (1.4); 7.1878 (0.6); 7.1830 (0.8); 7.1509 (0.4); 7.0898 (2.6); 7.0627 (1.8); 5.5643 (1.4); 4.6248 (0.4); 4.6137 (0.5); 4.6079 (0.5); 4.5974 (0.6); 4.5864 (0.5); 4.5751 (0.4); 4.1706 (0.6); 4.1468 (0.6); 3.8593 (0.8); 3.8486 (0.8); 3.8209 (1.6); 3.8103 (1.5); 3.7530 (1.5); 3.7360 (1.5); 3.7145 (0.8); 3.6975 (0.8); 3.0487 (0.4); 3.0280 (0.3); 3.0048 (1.7); 2.9942 (1.8); 2.9827 (1.7); 2.9673 (1.7); 2.8404 (0.6); 2.7494 (16.0); 2.7023 (0.4); 2.4578 (1.4); 2.4371 (11.6); 2.4009 (0.4); 2.0828 (2.4); 1.6224 (0.7); 1.3204 (0.8); 1.2965 (1.5); 1.2727 (0.7); 0.1072 (1.8); 0.0476 (0.5); 0.0460 (0.3); 0.0444 (0.4); 0.0368 (15.1); 0.0276 (0.5); 0.0259 (0.5) 4-45: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1411 (5.4); 8.1244 (0.8); 8.0974 (0.7); 7.4247 (0.7); 7.4176 (0.8); 7.4031 (0.8); 7.3990 (1.0); 7.3922 (1.6); 7.3813 (0.8); 7.3705 (0.9); 7.2988 (10.9); 7.2644 (0.4); 7.2574 (0.5); 7.2369 (1.6); 7.2299 (1.3); 7.2193 (4.2); 7.2097 (1.3); 7.1968 (1.4); 7.1933 (1.4); 7.1658 (0.5); 7.0152 (2.4); 6.9906 (0.6); 6.9646 (2.3); 6.9593 (2.4); 6.9520 (3.4); 6.9261 (0.6); 5.6229 (0.4); 4.7434 (0.4); 4.7308 (0.5); 4.7217 (0.6); 4.7160 (0.6); 4.7091 (0.6); 4.7036 (0.6); 4.6944 (0.5); 4.6819 (0.4); 4.1707 (0.8); 4.1469 (0.8); 4.1233 (0.3); 3.8816 (0.9); 3.8692 (0.9); 3.8437 (1.6); 3.8313 (1.5); 3.7556 (1.5); 3.7343 (1.4); 3.7178 (0.9); 3.6964 (0.9); 2.9484 (3.0); 2.9259 (3.2); 2.7434 (16.0); 2.1864 (12.1); 2.1795 (12.5); 2.0834 (4.0); 1.6494 (1.0); 1.3206 (1.0); 1.2968 (2.0); 1.2729 (1.0); 0.1068 (2.0); 0.0474 (0.5); 0.0366 (13.4); 0.0258 (0.7) 4-46: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.3531 (0.7); 8.3271 (0.7); 8.1514 (5.2); 7.6115 (0.5); 7.5891 (1.0); 7.5688 (0.6); 7.5004 (0.4); 7.4738 (1.0); 7.4710 (1.0); 7.4499 (0.7); 7.4001 (1.1); 7.3726 (1.4); 7.3459 (0.5); 7.2986 (15.7); 7.1288 (1.1); 7.0852 (1.8); 7.0591 (2.0); 6.9464 (2.1); 6.8622 (2.0); 6.7713 (1.2); 6.7644 (2.0); 6.7457 (1.0); 6.7395 (0.9); 5.5759 (3.2); 5.3378 (10.7); 4.6672 (0.4); 4.6556 (0.5); 4.6479 (0.5); 4.6398 (0.6); 4.6140 (0.4); 3.8659 (0.8); 3.8545 (0.8); 3.8280 (1.6); 3.8167 (1.4); 3.7634 (1.5); 3.7449 (1.4); 3.7255 (0.8); 3.7071 (0.7); 2.9953 (2.6); 2.9742 (1.8); 2.9682 (1.8); 2.7447 (16.0); 2.4533 (0.7); 2.4060 (10.8); 2.3844 (0.3); 1.8342 (0.5); 1.8231 (0.5); 1.8064 (1.0); 1.7893 (0.6); 1.7783 (0.6); 1.6031 (8.1); 0.9668 (0.7); 0.9523 (1.8); 0.9454 (2.0); 0.9390 (1.0); 0.9312 (1.1); 0.9239 (1.9); 0.9173 (1.8); 0.9033 (0.9); 0.6652 (0.9); 0.6507 (2.1); 0.6480 (1.8); 0.6445 (1.9); 0.6339 (2.0); 0.6288 (2.1); 0.6126 (0.7); 0.1071 (0.5); 0.0482 (0.7); 0.0374 (21.3); 0.0265 (0.9) 4-47: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.2539 (0.8); 8.2264 (0.8); 8.1553 (5.3); 7.6054 (0.6); 7.5792 (1.7); 7.5530 (1.3); 7.4885 (1.6); 7.4628 (0.9); 7.3589 (1.9); 7.3268 (1.1); 7.3238 (1.2); 7.3199 (1.0); 7.2987 (5.0); 7.0150 (2.6); 6.9528 (6.2); 6.9062 (1.1); 6.7184 (2.3); 6.5306 (1.2); 5.6022 (3.1); 5.3353 (4.2); 4.7319 (0.4); 4.7193 (0.5); 4.7103 (0.6); 4.7047 (0.5); 4.6976 (0.6); 4.6922 (0.6); 4.6831 (0.5); 4.6708 (0.4); 3.8731 (0.9); 3.8608 (0.9); 3.8354 (1.6); 3.8231 (1.5); 3.7479 (1.5); 3.7270 (1.5); 3.7101 (0.9); 3.6892 (0.9); 2.9442 (3.1); 2.9215 (3.2); 2.7437 (16.0); 2.1949 (11.9); 2.1791 (12.0); 1.6631 (1.4); 0.0371 (5.4) 4-48: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.4737 (0.7); 8.4469 (0.7); 8.1580 (5.3); 7.6170 (0.6); 7.5907 (1.6); 7.5647 (1.2); 7.4925 (1.4); 7.4667 (0.9); 7.3951 (1.7); 7.3691 (1.0); 7.3658 (1.1); 7.3621 (0.9); 7.3425 (0.8); 7.3390 (0.8); 7.3351 (0.7); 7.3315 (0.6); 7.2987 (8.0); 7.0753 (1.8); 7.0494 (2.1); 6.9163 (1.1); 6.8760 (1.9); 6.8715 (2.0); 6.7773 (1.2); 6.7716 (1.1); 6.7514 (1.0); 6.7454 (0.9); 6.7285 (2.2); 6.5407 (1.1); 5.5584 (4.0); 5.3368 (10.1); 4.6500 (0.4); 4.6390 (0.4); 4.6326 (0.5); 4.6233 (0.5); 4.6119 (0.4); 4.5981 (0.4); 3.8579 (0.7); 3.8467 (0.8); 3.8203 (1.6); 3.8090 (1.4); 3.7587 (1.5); 3.7407 (1.4); 3.7209 (0.8); 3.7030 (0.7); 2.9848 (2.3); 2.9639 (1.8); 2.9572 (1.8); 2.7440 (16.0); 2.4501 (0.6); 2.4037 (11.0); 1.8501 (0.5); 1.8388 (0.5); 1.8221 (1.0); 1.8052 (0.6); 1.7941 (0.6); 1.6237 (4.3); 0.9737 (0.7); 0.9593 (1.8); 0.9523 (2.0); 0.9457 (0.9); 0.9384 (1.0); 0.9309 (1.9); 0.9243 (1.7); 0.9104 (0.8); 0.6761 (0.9); 0.6619 (2.0); 0.6586 (1.8); 0.6451 (1.9); 0.6402 (1.9); 0.6241 (0.7); 0.0482 (0.4); 0.0375 (10.8); 0.0266 (0.4) 4-49: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.3383 (0.8); 8.3119 (0.8); 8.1497 (5.3); 7.8904 (0.4); 7.7933 (0.4); 7.6111 (0.5); 7.5877 (1.0); 7.5659 (0.6); 7.4958 (0.5); 7.4715 (1.1); 7.4691 (1.0); 7.4477 (0.8); 7.3979 (1.2); 7.3709 (1.4); 7.3442 (0.5); 7.2986 (4.4); 7.1259 (1.1); 7.0857 (1.8); 7.0601 (2.2); 6.9600 (2.1); 6.9434 (2.3); 6.8850 (1.2); 6.8597 (1.0); 6.7609 (1.1); 5.5870 (3.0); 5.3357 (10.2); 4.6853 (0.4); 4.6739 (0.5); 4.6668 (0.5); 4.6573 (0.6); 4.6473 (0.5); 4.6405 (0.5); 4.6293 (0.4); 4.1836 (0.4); 3.8744 (0.8); 3.8630 (0.8); 3.8366 (1.7); 3.8253 (1.5); 3.7729 (1.5); 3.7544 (1.5); 3.7351 (0.8); 3.7165 (0.8); 3.0026 (3.4); 2.9784 (3.3); 2.7409 (16.0); 2.4043 (11.5); 2.3840 (0.4); 2.2581 (10.7); 1.6489 (1.6); 0.0367 (6.0) 4-50: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1521 (4.0); 8.1305 (0.6); 8.1029 (0.5); 7.6110 (0.4); 7.5885 (0.7); 7.5696 (0.4); 7.4669 (0.3); 7.4402 (0.8); 7.4196 (0.6); 7.3918 (1.0); 7.3649 (1.1); 7.3378 (0.4); 7.2989 (11.6); 7.1178 (0.8); 7.0173 (1.7); 6.9915 (0.5); 6.9653 (1.5); 6.9603 (1.5); 6.9477 (2.3); 6.9354 (1.8); 6.9221 (0.6); 6.7529 (0.8); 5.6231 (1.8); 5.3383 (5.3); 4.7373 (0.4); 4.7279 (0.4); 4.7220 (0.4); 4.7154 (0.4); 4.7096 (0.4); 4.7006 (0.4); 3.8820 (0.7); 3.8696 (0.7); 3.8441 (1.2); 3.8317 (1.1); 3.7533 (1.1); 3.7318 (1.1); 3.7153 (0.7); 3.6940 (0.6); 2.9518 (2.4); 2.9295 (2.4); 2.7460 (12.1); 2.1747 (16.0); 1.6073 (7.8); 0.0480 (0.6); 0.0372 (15.6); 0.0263 (0.7) 4-51: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.5932 (0.9); 8.5672 (0.9); 8.1311 (0.7); 8.1206 (5.2); 7.2990 (18.0); 7.2211 (1.2); 7.2149 (1.0); 7.1940 (1.6); 7.1879 (1.5); 7.1711 (0.5); 7.1441 (3.7); 7.1259 (3.2); 7.0923 (3.1); 7.0650 (1.9); 6.8781 (0.8); 6.8618 (1.2); 6.8564 (1.0); 6.8470 (1.2); 6.8332 (0.8); 6.8243 (0.6); 5.6126 (0.3); 5.5706 (5.4); 5.3381 (0.5); 4.6377 (0.5); 4.6118 (0.7); 4.5977 (0.6); 4.5863 (0.5); 3.8636 (0.8); 3.8525 (0.9); 3.8254 (1.7); 3.8144 (1.6); 3.7556 (1.6); 3.7381 (1.6); 3.7175 (0.9); 3.6999 (0.8); 3.0398 (0.4); 3.0174 (0.4); 2.9928 (3.1); 2.9707 (2.3); 2.9658 (2.4); 2.8414 (1.1); 2.7395 (16.0); 2.6943 (0.8); 2.4596 (1.8); 2.4342 (12.6); 2.1741 (0.6); 2.1627 (0.6); 2.1458 (1.1); 2.1285 (0.7); 2.1171 (0.6); 2.1001 (0.3); 1.5988 (13.5); 1.2917 (0.6); 1.1017 (0.6); 1.0863 (1.9); 1.0797 (2.2); 1.0652 (1.2); 1.0580 (2.0); 1.0515 (2.2); 1.0372 (1.0); 0.8398 (0.9); 0.8197 (2.6); 0.8080 (2.3); 0.8023 (2.7); 0.7861 (0.9); 0.1072 (5.3); 0.0481 (0.8); 0.0375 (22.2) 4-52: ¹H-NMR(300.2 MHz, CDCl3): δ = 9.2470 (1.9); 9.2200 (1.9); 8.3241 (16.0); 8.3046 (2.5); 8.1121 (0.6); 8.1045 (0.6); 8.0472 (0.5); 8.0382 (0.5); 7.9332 (5.7); 7.9254 (5.9); 7.7161 (0.5); 7.6893 (7.5); 7.6720 (12.5); 7.6131 (0.8); 7.6042 (1.2); 7.5972 (4.2); 7.5888 (4.1); 7.5692 (7.6); 7.5612 (9.9); 7.5290 (1.0); 7.5154 (2.6); 7.5072 (2.7); 7.5016 (3.6); 7.4955 (3.1); 7.4861 (2.3); 7.4774 (1.6); 7.3917 (0.4); 7.3722 (0.5); 7.2991 (26.8); 7.2209 (0.9); 7.1909 (6.8); 7.1632 (5.4); 6.6003 (0.6); 6.5817 (0.5); 5.6810 (1.0); 5.3374 (5.6); 5.0383 (0.4); 5.0192 (1.3); 5.0104 (0.7); 5.0003 (2.2); 4.9918 (1.6); 4.9817 (1.7); 4.9728 (2.1); 4.9632 (0.7); 4.9543 (1.4); 4.9354 (0.4); 4.8914 (0.4); 4.8693 (0.4); 4.2712 (0.5); 4.2559 (0.5); 4.2130 (0.6); 4.1948 (1.4); 4.1702 (2.7); 4.1583 (0.4); 4.1464 (2.7); 4.1228 (1.2); 4.1014 (0.7); 4.0907 (0.4); 4.0788 (0.4); 4.0733 (0.4); 3.7480 (12.6); 3.7282 (11.7); 3.2718 (1.6); 3.2544 (1.6); 3.2219 (4.8); 3.2047 (4.5); 3.1648 (4.2); 3.1466 (4.2); 3.1152 (1.7); 3.0971 (1.7); 2.0826 (13.7); 2.0451 (0.8); 1.7621 (3.5); 1.7585 (2.8); 1.7437 (3.5); 1.7388 (2.6); 1.6708 (1.4); 1.6490 (1.4); 1.4517 (0.3); 1.4294 (0.4); 1.4035 (0.4); 1.3201 (3.5); 1.2963 (7.0); 1.2725 (3.2); 0.9964 (0.6); 0.9719 (1.0); 0.9467 (0.6); 0.9213 (0.5); 0.9036 (0.4); 0.1186 (0.4); 0.1064 (11.0); 0.0471 (1.5); 0.0363 (36.8); 0.0256 (1.8) 4-53: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.3852 (1.1); 8.3591 (1.1); 8.3338 (10.3); 7.6531 (3.5); 7.6480 (2.4); 7.6389 (5.0); 7.6358 (5.8); 7.4946 (2.7); 7.4725 (0.4); 7.4591 (1.2); 7.4500 (1.1); 7.4447 (1.7); 7.4385 (1.4); 7.4292 (1.1); 7.4204 (0.7); 7.2988 (15.4); 6.7705 (5.4); 5.5580 (4.5); 5.0161 (0.4); 4.6575 (0.6); 4.6463 (0.6); 4.6393 (0.8); 4.6287 (0.9); 4.6200 (0.7); 4.6128 (0.7); 4.6021 (0.6); 3.8835 (1.1); 3.8723 (1.2); 3.8452 (2.7); 3.8340 (2.5); 3.7953 (2.5); 3.7770 (2.4); 3.7570 (1.2); 3.7387 (1.1); 2.9333 (4.5); 2.9096 (4.8); 2.3255 (16.0); 2.1521 (16.0); 1.6024 (4.5); 1.3157 (5.4); 1.2948 (5.5); 0.1075 (1.8); 0.0483 (0.9); 0.0375 (21.8); 0.0265 (0.8) 4-54: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.3508 (0.8); 8.3239 (0.8); 8.1300 (5.3); 7.3696 (1.2); 7.3434 (2.6); 7.3171 (1.6); 7.2986 (8.8); 7.0266 (1.8); 7.0133 (2.9); 6.9861 (0.4); 6.9545 (7.4); 6.9351 (1.0); 6.9274 (1.6); 6.9055 (1.9); 6.8998 (2.4); 5.6023 (0.9); 4.7241 (0.4); 4.7116 (0.5); 4.7028 (0.6); 4.6973 (0.6); 4.6900 (0.6); 4.6753 (0.5); 4.6629 (0.4); 4.1944 (0.8); 4.1706 (2.3); 4.1468 (2.3); 4.1231 (0.8); 3.8609 (0.9); 3.8484 (0.9); 3.8232 (1.6); 3.8108 (1.5); 3.7321 (1.5); 3.7108 (1.5); 3.6944 (0.9); 3.6732 (0.9); 2.9262 (2.8); 2.9034 (3.0); 2.8407 (1.1); 2.7305 (16.0); 2.2065 (12.1); 2.1829 (12.3); 2.0831 (10.3); 1.9962 (0.3); 1.9796 (0.6); 1.9682 (0.7); 1.9516 (1.2); 1.9350 (0.7); 1.9237 (0.7); 1.9068 (0.3); 1.6501 (2.0); 1.3204 (2.8); 1.2966 (5.6); 1.2728 (2.7); 1.0628 (0.7); 1.0481 (1.9); 1.0411 (2.2); 1.0265 (1.2); 1.0197 (2.0); 1.0132 (1.9); 0.9987 (0.9); 0.7797 (0.9); 0.7649 (2.5); 0.7602 (2.1); 0.7482 (2.2); 0.7433 (2.4); 0.7268 (0.8); 0.1069 (2.2); 0.0473 (0.4); 0.0365 (11.5); 0.0256 (0.5) 4-55: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.6557 (0.8); 8.6299 (0.8); 8.1587 (0.4); 8.1283 (0.7); 8.1206 (5.2); 7.3836 (1.1); 7.3574 (2.6); 7.3310 (1.7); 7.3176 (2.1); 7.3115 (2.4); 7.2993 (15.6); 7.2149 (1.0); 7.2082 (0.9); 7.1878 (1.4); 7.1809 (1.4); 7.0692 (2.7); 7.0420 (2.2); 7.0290 (1.7); 7.0030 (1.5); 6.9893 (1.2); 6.9866 (1.2); 6.9815 (1.5); 6.9788 (1.4); 6.9600 (1.0); 6.9549 (1.4); 6.9521 (1.3); 6.9337 (2.1); 6.9276 (2.6); 5.5388 (1.0); 4.6156 (0.4); 4.5986 (0.5); 4.5886 (0.6); 4.5749 (0.5); 4.5631 (0.4); 4.1948 (0.6); 4.1709 (1.7); 4.1471 (1.8); 4.1233 (0.6); 3.8431 (0.8); 3.8322 (0.8); 3.8052 (1.6); 3.7942 (1.5); 3.7390 (1.5); 3.7219 (1.5); 3.7009 (0.8); 3.6839 (0.8); 3.0187 (0.3); 2.9962 (0.4); 2.9738 (2.1); 2.9692 (2.2); 2.9510 (1.9); 2.9423 (1.9); 2.8411 (0.4); 2.7572 (1.6); 2.7365 (16.0); 2.4499 (1.0); 2.4247 (11.8); 2.3849 (0.4); 2.3250 (1.0); 2.0836 (7.6); 2.0046 (0.3); 1.9876 (0.6); 1.9766 (0.7); 1.9599 (1.3); 1.9431 (0.8); 1.9320 (0.8); 1.9148 (0.4); 1.6548 (0.9); 1.5550 (0.3); 1.3209 (2.1); 1.2971 (4.2); 1.2733 (2.1); 1.0708 (0.7); 1.0545 (1.8); 1.0490 (2.2); 1.0342 (1.3); 1.0270 (2.2); 1.0206 (2.1); 1.0064 (1.1); 0.7875 (1.0); 0.7724 (2.6); 0.7660 (2.4); 0.7560 (2.5); 0.7497 (2.7); 0.7341 (1.1); 0.1069 (4.1); 0.0478 (0.6); 0.0369 (19.1); 0.0261 (1.0) 4-56: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.3067 (0.9); 8.2790 (0.8); 8.0914 (5.2); 8.0822 (0.4); 7.3771 (1.2); 7.3509 (2.7); 7.3246 (1.7); 7.2986 (3.9); 7.1651 (2.3); 7.1388 (2.6); 7.0338 (4.0); 7.0285 (3.9); 7.0058 (1.4); 6.9897 (1.2); 6.9867 (1.1); 6.9818 (1.4); 6.9630 (1.0); 6.9598 (1.0); 6.9552 (1.4); 6.9329 (1.9); 6.9270 (2.4); 6.9203 (1.3); 6.8143 (1.5); 6.8085 (1.4); 6.7881 (1.3); 6.7822 (1.2); 5.6043 (0.5); 4.8376 (0.4); 4.8249 (0.4); 4.8164 (0.5); 4.8042 (0.5); 4.7889 (0.4); 4.7767 (0.4); 4.1917 (0.5); 4.1679 (1.5); 4.1441 (1.5); 4.1204 (0.5); 3.9070 (0.9); 3.8945 (1.0); 3.8695 (1.6); 3.8572 (1.4); 3.7608 (1.4); 3.7402 (1.4); 3.7234 (0.9); 3.7028 (0.9); 3.0840 (2.0); 3.0769 (2.0); 3.0618 (1.8); 3.0516 (1.8); 2.8379 (4.4); 2.7471 (0.4); 2.7163 (16.0); 2.0803 (6.7); 2.0031 (0.3); 1.9864 (0.6); 1.9750 (0.7); 1.9584 (1.3); 1.9417 (0.8); 1.9304 (0.8); 1.9136 (0.4); 1.8631 (0.4); 1.8460 (0.6); 1.8347 (0.7); 1.8181 (1.2); 1.8014 (0.7); 1.7902 (0.7); 1.7733 (0.4); 1.3178 (1.8); 1.2940 (3.7); 1.2702 (1.8); 1.0640 (0.8); 1.0489 (2.1); 1.0419 (2.3); 1.0363 (1.2); 1.0270 (1.4); 1.0205 (2.3); 1.0139 (2.2); 1.0043 (1.0); 0.9992 (1.3); 0.9895 (2.1); 0.9827 (2.3); 0.9680 (1.1); 0.9610 (2.1); 0.9547 (2.0); 0.9402 (0.9); 0.7893 (0.9); 0.7742 (2.6); 0.7690 (2.3); 0.7576 (2.2); 0.7522 (2.8); 0.7356 (0.8); 0.6778 (0.9); 0.6629 (2.4); 0.6583 (2.0); 0.6462 (2.1); 0.6414 (2.4); 0.6250 (0.8); 0.1068 (1.1); 0.0349 (5.2) 4-57: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1097 (5.4); 8.0920 (0.8); 8.0642 (0.8); 7.9214 (0.4); 7.9111 (0.4); 7.8930 (0.5); 7.7952 (0.5); 7.7856 (0.3); 7.7771 (0.4); 7.7667 (0.4); 7.6141 (0.5); 7.5905 (1.0); 7.5690 (0.6); 7.5121 (0.5); 7.4876 (1.1); 7.4635 (0.8); 7.4029 (1.2); 7.3759 (1.5); 7.3490 (0.5); 7.2985 (10.6); 7.1962 (2.1); 7.1703 (2.5); 7.1327 (2.4); 6.9433 (2.9); 6.9252 (1.1); 6.7603 (1.1); 5.6266 (3.3); 5.3373 (13.4); 4.8692 (0.4); 4.8568 (0.4); 4.8484 (0.5); 4.8355 (0.5); 4.8211 (0.4); 4.8091 (0.4); 4.1807 (0.4); 3.9366 (1.0); 3.9243 (1.0); 3.8990 (1.6); 3.8868 (1.5); 3.7989 (1.5); 3.7785 (1.5); 3.7612 (1.0); 3.7410 (0.9); 3.1193 (3.2); 3.0943 (2.3); 2.7300 (16.0); 2.2696 (11.4); 1.6096 (4.4); 0.0471 (0.5); 0.0455 (0.4); 0.0363 (14.4); 0.0287 (0.5); 0.0271 (0.5); 0.0255 (0.5)

TABLE 11 Compounds according to formula (6)

(6) In table 11, ″#″ denotes the point of attachment to the L-R⁶ group and ″*″ denotes the point of attachment to the pyridazin-4-yl group. Ex No R⁷ R⁸ X

L-R⁶ LogP 6- 01 Cl H Cl

— (2,4-dimethyl- phenyl)methyl 3.72^([a]) 6- 02 Cl H Cl —

(2,4-dimethyl- phenyl)methyl 1.93^([a]) 6- 03 Cl CH₃ Cl —

(2,4-dimethyl- phenyl)methyl 1.96^([a]) 6- 04 Cl CH₃ Cl

— (2,4-dimethyl- phenyl)methyl 3.79^([a]) 6- 05 CH₃ H Cl

— (2,4-dimethyl- phenyl)methyl 3.17^([a]) 6- 06 CH₃ H Cl —

(2,4-dimethyl- phenyl)methyl 1.53^([a]) 6- 07 Cl H Cl —

(2,4-dichloro- phenyl)methyl 2.30^([a]) 6- 08 Cl H Cl —

(4-bromo-2- chloro- phenyl)methyl 2.40^([a])

TABLE 12 6-01: 1H-NMR(300.2 MHz, CDCl3): δ = 8.2099 (0.5); 7.8978 (2.5); 7.8864 (2.8); 7.8813 (2.6); 7.8775 (3.2); 7.8684 (5.9); 7.8540 (2.8); 7.8391 (6.0); 7.8304 (3.4); 7.8267 (3.4); 7.8211 (3.9); 7.8102 (3.2); 7.7920 (1.7); 7.7731 (0.8); 7.7607 (9.1); 7.2991 (10.6); 7.2605 (2.1); 7.2355 (2.6); 7.0697 (6.2); 7.0444 (1.6); 4.6013 (1.4); 4.5909 (2.2); 4.5587 (2.6); 4.5329 (0.6); 4.5213 (0.4); 4.1646 (1.7); 4.1405 (1.5); 4.1325 (1.0); 3.2737 (0.7); 3.2525 (0.7); 3.2282 (1.5); 3.2072 (1.4); 3.1614 (1.6); 3.1314 (1.5); 3.1159 (0.8); 3.0850 (0.7); 2.8360 (3.4); 2.5356 (0.4); 2.4648 (16.0); 2.4377 (0.5); 2.3529 (14.9); 2.3192 (1.1); 1.6452 (13.9); 1.2914 (0.3); 0.1072 (1.2); 0.0473 (0.5); 0.0365 (10.6); 0.0258 (0.6) 6-02: 1H-NMR(300.2 MHz, CDCl3): δ = 7.7365 (6.3); 7.4863 (0.9); 7.4609 (0.9); 7.2997 (10.2); 7.1523 (0.4); 7.1169 (2.2); 7.0916 (3.4); 7.0689 (0.6); 7.0430 (3.6); 7.0044 (2.4); 6.9780 (1.5); 5.6118 (0.9); 4.5915 (0.6); 4.5801 (0.7); 4.5755 (0.7); 4.5652 (0.9); 4.5520 (0.7); 4.5409 (0.6); 3.8608 (0.9); 3.8510 (1.0); 3.8223 (2.2); 3.8125 (2.1); 3.7881 (0.4); 3.7795 (0.4); 3.7678 (2.1); 3.7514 (2.2); 3.7293 (1.1); 3.7130 (1.0); 3.0153 (3.4); 2.9950 (2.4); 2.9864 (2.6); 2.9704 (0.6); 2.9408 (0.5); 2.4268 (15.5); 2.3947 (0.8); 2.3688 (0.4); 2.3344 (16.0); 2.3055 (0.8); 2.0827 (0.4); 2.0538 (0.5); 2.0463 (0.4); 1.6254 (2.2); 1.2920 (1.1); 0.1076 (0.9); 0.0474 (0.4); 0.0378 (12.2) 6-03: 1H-NMR(300.2 MHz, CDCl3): δ = 7.2991 (3.5); 7.2693 (0.9); 7.0968 (1.7); 7.0713 (2.5); 7.0177 (2.3); 6.9780 (1.4); 6.9525 (1.0); 5.6453 (2.4); 5.3355 (5.7); 4.7585 (0.4); 4.7478 (0.4); 4.7288 (0.6); 4.7102 (0.4); 4.7031 (0.4); 4.0194 (1.2); 3.8879 (0.8); 3.8762 (0.8); 3.8505 (1.6); 3.8388 (1.5); 3.7887 (1.5); 3.7683 (1.5); 3.7512 (0.8); 3.7308 (0.8); 3.0130 (0.4); 2.9888 (0.4); 2.9662 (1.4); 2.9415 (1.5); 2.9341 (1.6); 2.9071 (1.3); 2.8869 (0.4); 2.8602 (0.4); 2.4098 (0.4); 2.3906 (12.0); 2.3676 (0.5); 2.3225 (11.7); 2.2559 (16.0); 2.1947 (1.2); 2.1032 (0.4); 1.3059 (0.8); 1.2851 (0.9); 0.0367 (3.1) 6-05: 1H-NMR(300.2 MHz, d6-DMSO): δ = 9.0523 (0.8); 9.0241 (0.8); 7.9728 (1.8); 7.9147 (0.6); 7.9025 (5.0); 7.8991 (5.2); 7.8867 (0.8); 7.5732 (3.0); 7.1726 (1.0); 7.1471 (1.2); 7.0074 (1.4); 6.9831 (0.8); 6.9572 (0.6); 4.4854 (0.4); 4.4659 (0.4); 4.2938 (1.8); 4.2756 (1.5); 3.3515 (16.0); 3.1042 (0.3); 3.0841 (0.4); 3.0568 (0.5); 3.0365 (0.4); 2.9109 (13.2); 2.8742 (0.5); 2.8456 (0.5); 2.8268 (0.4); 2.7984 (0.3); 2.7516 (11.0); 2.7092 (1.6); 2.6716 (7.8); 2.5284 (2.1); 2.5224 (2.9); 2.5166 (2.1); 2.3343 (6.0); 2.2611 (5.6); 0.0199 (2.5) 6-06: 1H-NMR(300.2 MHz, CDCl3): δ = 7.6200 (4.8); 7.4446 (0.6); 7.4168 (0.6); 7.2987 (7.6); 7.1318 (1.6); 7.1062 (2.3); 7.0390 (2.2); 7.0006 (1.4); 6.9752 (1.0); 5.6037 (2.5); 5.3375 (1.5); 4.5950 (0.4); 4.5844 (0.5); 4.5733 (0.5); 4.5677 (0.6); 4.5566 (0.6); 4.5457 (0.4); 3.8533 (0.8); 3.8431 (0.8); 3.8151 (1.7); 3.8050 (1.6); 3.7606 (1.6); 3.7441 (1.6); 3.7225 (0.8); 3.7061 (0.8); 3.0473 (0.3); 3.0238 (1.6); 3.0046 (2.3); 2.9777 (1.5); 2.9608 (0.3); 2.9320 (0.4); 2.7799 (16.0); 2.4318 (12.0); 2.4025 (0.4); 2.3307 (11.0); 1.6229 (0.7); 0.1067 (0.8); 0.0474 (0.4); 0.0368 (10.0); 0.0261 (0.4) 6-07: 1H-NMR(400.2 MHz, d6-DMSO): δ = 8.8676 (2.8); 8.8455 (3.0); 8.8348 (0.6); 8.8315 (0.5); 8.8133 (0.4); 8.7923 (0.3); 8.2245 (0.8); 8.0032 (16.0); 7.5994 (6.4); 7.4597 (0.4); 7.4542 (0.4); 7.4454 (0.4); 7.4218 (0.7); 7.4174 (0.4); 7.3972 (15.4); 7.3784 (0.6); 6.2059 (3.3); 4.5405 (0.7); 4.5280 (1.0); 4.5174 (1.4); 4.5049 (1.4); 4.4945 (1.0); 4.4820 (0.7); 3.6675 (1.2); 3.6519 (1.3); 3.6408 (3.5); 3.6252 (3.9); 3.6204 (3.8); 3.6058 (3.4); 3.5936 (1.4); 3.5792 (1.1); 3.3400 (0.6); 3.0866 (1.8); 3.0744 (1.9); 3.0513 (2.4); 3.0391 (2.2); 2.8077 (2.2); 2.7838 (2.2); 2.7724 (1.8); 2.7485 (1.7); 2.5148 (4.0); 2.5105 (7.8); 2.5061 (10.1); 2.5016 (7.2); 2.4974 (3.4); 0.0001 (1.3) 6-08: 1H-NMR(300.1 MHz, d6-DMSO): δ = 8.8488 (2.4); 8.8194 (2.4); 7.9916 (16.0); 7.7106 (6.1); 7.7038 (6.5); 7.5395 (2.9); 7.5328 (2.6); 7.5121 (3.7); 7.5054 (3.5); 7.3382 (5.6); 7.3107 (4.4); 6.1450 (10.9); 4.5456 (0.6); 4.5285 (0.8); 4.5144 (1.2); 4.4983 (1.2); 4.4844 (0.8); 4.4675 (0.6); 3.6722 (0.8); 3.6514 (0.9); 3.6366 (3.3); 3.6183 (4.6); 3.6005 (3.1); 3.5844 (0.9); 3.5650 (0.7); 3.3187 (6.9); 3.0769 (1.4); 3.0605 (1.4); 3.0299 (2.0); 3.0136 (1.8); 2.8016 (1.8); 2.7699 (1.8); 2.7545 (1.4); 2.7228 (1.3); 2.5143 (2.4); 2.5084 (4.7); 2.5024 (6.1); 2.4964 (4.2); 2.4906 (1.9); 2.0753 (0.4); −0.0004 (7.0)

TABLE 13 Compounds according to formula (7)

(7) In table 13, ″#″ denotes the point of attachment to the L-R⁶ group and ″*″ denotes the point of attachment to the pyridazin-4-yl group. Ex No R⁷ R⁸ X

L-R⁶ LogP 7-01 (*) Cl H Cl

(2,4-dimethylphenyl)methyl 2.98^([a]) 7-02 Cl CH₃ Cl

(2,4-dimethylphenyl)methyl 3.00^([a]) 7-03 (*) CH₃ H Cl

(2,4-dimethylphenyl)methyl 2.45^([a]) 7-04 (*) CH₃ H Cl

(2,4-dimethylphenyl)methyl 2.44^([a]) 7-05 (*) Cl H Cl

(2,4-dichlorophenyl)methyl 3.17^([a]) 7-06 (*) Cl H Cl

(4-bromo-2-chloro- phenyl)methyl 3.28^([a]) 7-07 (*) Cl H Cl

(2,4-dichlorophenyl)methyl 3.19^([a]) 7-08 (*) Cl H Cl

(2,4-dichlorophenyl)methyl 3.19^([a]) 7-09 (*) Cl H Cl

(4-bromo-2-chloro- phenyl)methyl 3.31^([a]) 7-10 (*) Cl H Cl

(4-bromo-2-chloro- phenyl)methyl 3.31^([a]) 7-11 (*) Cl H Cl

(2,4-dimethylphenyl)methyl 3.04^([a]) 7-12 (*) Cl H Cl

(2,4-dimethylphenyl)methyl 3.04^([a]) (*) Ex 7-07 and 7-08 are the 2 enantiomers of Ex 7-05 Ex 7-07: Optical rotation: +61.9° (c = 2.23, CDCl3, 20° C.); concentration c is expressed in g/100 mL. Ex 7-08: Optical rotation: −59.6° (c = 2.45, CDCl3, 20° C.); concentration c is expressed in g/100 mL. (*) Ex 7-09 and 7-10 are the 2 enantiomers of Ex 7-06 Ex 7-09: Optical rotation: +62.4° (c = 2.28, CDCl3, 20° C.); concentration c is expressed in g/100 mL. Ex 7-10: Optical rotation: −59.6° (c = 2.35, CDCl3, 20° C.); concentration c is expressed in g/100 mL. (*) Ex 7-11 and 7-12 are the 2 enantiomers of Ex 7-01 Ex 7-11: Optical rotation: −90.1° (c = 2.18, CDCl3, 20° C.); concentration c is expressed in g/100 mL. Ex 7-12: Optical rotation: +93.2° (c = 1.83, CDCl3, 20° C.); concentration c is expressed in g/100 mL. (*) Ex 7-03 is Single Stereoisomer; Ex 7-04 is racemate

TABLE 14 7-01: 1H-NMR(300.2 MHz, CDCl3): δ = 7.7686 (8.3); 7.7444 (0.7); 7.2987 (6.5); 7.1869 (0.4); 7.1608 (0.4); 7.0830 (1.5); 7.0568 (6.5); 7.0283 (2.4); 7.0021 (1.0); 5.1557 (1.6); 4.1917 (1.0); 4.1832 (1.6); 4.1652 (0.6); 4.1570 (1.8); 4.1479 (1.4); 4.1423 (0.8); 3.9419 (0.5); 3.9324 (0.8); 3.9231 (0.9); 3.9135 (1.0); 3.9046 (1.1); 3.8897 (2.5); 3.8722 (0.7); 3.8552 (1.8); 3.8368 (1.0); 3.0482 (0.8); 3.0295 (0.8); 3.0205 (0.4); 3.0028 (1.6); 2.9833 (1.5); 2.8882 (1.3); 2.8600 (1.3); 2.8421 (1.0); 2.8139 (0.9); 2.4274 (1.3); 2.3479 (16.0); 2.3293 (15.0); 2.0792 (2.4); 1.6221 (1.2); 1.3191 (0.6); 1.2952 (1.2); 1.2714 (0.5); 0.1071 (0.7); 0.0368 (7.6) 7-02: 1H-NMR(300.2 MHz, CDCl3): δ = 7.2986 (9.5); 7.1704 (0.3); 7.0662 (1.2); 7.0399 (3.6); 7.0011 (1.4); 6.9745 (0.6); 4.9509 (1.0); 4.1927 (0.6); 4.1828 (1.0); 4.1569 (1.1); 4.1477 (0.8); 4.1012 (0.4); 3.9669 (0.5); 3.9573 (0.6); 3.9477 (0.6); 3.9392 (0.8); 3.9287 (1.5); 3.9121 (0.4); 3.8937 (1.0); 3.8762 (0.6); 3.0600 (0.5); 3.0402 (0.5); 3.0143 (1.2); 2.9944 (1.1); 2.9229 (0.8); 2.8952 (0.8); 2.8767 (0.6); 2.8489 (0.5); 2.5357 (16.0); 2.4138 (0.8); 2.4101 (1.5); 2.3656 (1.4); 2.3469 (11.4); 2.3118 (10.0); 2.2791 (2.2); 2.2677 (1.1); 2.2591 (2.3); 1.9072 (1.4); 1.9006 (1.6); 1.8791 (2.0); 1.8171 (0.4); 1.7937 (2.0); 1.6050 (2.4); 1.3137 (1.4); 1.2926 (3.0); 0.1068 (0.5); 0.0478 (0.4); 0.0370 (11.4); 0.0260 (0.4) 7-03: 1H-NMR(300.2 MHz, CDCl3): δ = 7.5488 (5.1); 7.3040 (0.6); 7.3003 (1.3); 7.2983 (1.5); 7.2941 (0.9); 7.0889 (1.6); 7.0636 (2.9); 7.0365 (3.4); 7.0110 (2.3); 6.9853 (1.2); 5.3719 (1.2); 4.1347 (1.4); 4.1085 (1.6); 4.1002 (1.3); 3.9197 (0.7); 3.9105 (0.8); 3.8798 (2.2); 3.8457 (1.4); 3.8279 (1.0); 3.0325 (0.6); 3.0129 (0.6); 2.9871 (1.4); 2.9667 (1.3); 2.9172 (1.1); 2.8905 (1.1); 2.8718 (0.8); 2.8443 (0.6); 2.7086 (16.0); 2.6614 (1.8); 2.3748 (0.6); 2.3421 (13.1); 2.3191 (12.8); 2.2094 (2.6); 1.3369 (0.4); 1.3029 (1.6); 1.2821 (6.9); 0.9134 (0.3); 0.8900 (0.3); 0.0387 (0.5); 0.0351 (1.2); 0.0332 (1.4); 0.0291 (0.8) 7-04: 1H-NMR(300.2 MHz, CDCl3): δ = 7.6408 (1.0); 7.5715 (4.8); 7.2988 (6.8); 7.1867 (0.7); 7.1604 (0.8); 7.1440 (0.4); 7.1183 (0.5); 7.0967 (1.2); 7.0712 (2.7); 7.0566 (2.2); 7.0314 (1.6); 7.0041 (1.0); 6.5721 (0.6); 6.5458 (0.6); 5.3372 (0.8); 5.0665 (1.1); 4.2669 (0.3); 4.1969 (0.4); 4.1886 (0.8); 4.1800 (1.2); 4.1540 (1.2); 4.1443 (1.2); 3.9390 (0.4); 3.9297 (0.6); 3.9202 (0.6); 3.9107 (0.7); 3.9016 (0.8); 3.8848 (2.0); 3.8669 (0.6); 3.8503 (1.3); 3.8316 (0.8); 3.0495 (0.6); 3.0311 (0.6); 3.0178 (0.4); 3.0039 (1.2); 2.9849 (1.2); 2.8930 (1.0); 2.8651 (0.9); 2.8470 (0.7); 2.8190 (0.7); 2.7773 (3.6); 2.7436 (16.0); 2.4360 (2.5); 2.3510 (11.6); 2.3315 (13.0); 2.0812 (0.9); 1.6260 (2.6); 1.2958 (0.5); 0.1069 (1.8); 0.0368 (9.1); 0.0260 (0.3) 7-05: 1H-NMR(300.1 MHz, d6-DMSO): δ = 8.2197 (16.0); 7.6184 (6.6); 7.6119 (7.2); 7.5499 (3.6); 7.5392 (3.7); 7.4737 (3.0); 7.4462 (8.5); 7.4229 (6.0); 7.4162 (5.5); 7.3954 (2.2); 7.3887 (2.2); 5.7586 (1.1); 3.8657 (3.5); 3.8339 (5.2); 3.8233 (3.3); 3.8069 (3.5); 3.7936 (3.4); 3.7680 (1.6); 3.7551 (0.8); 3.4504 (0.3); 3.4426 (0.3); 3.0545 (0.7); 3.0309 (0.7); 3.0099 (3.4); 2.9929 (4.5); 2.9860 (4.2); 2.9733 (3.6); 2.9491 (0.7); 2.9271 (0.5); 2.5127 (5.5); 2.5070 (6.9); 2.5014 (5.0); 1.9933 (0.8); 1.2849 (0.5); 1.2299 (0.5); 1.1782 (0.5); 0.9138 (0.5); 0.8885 (0.3); 0.8776 (0.6); 0.8621 (0.5); 0.8544 (0.6); 0.8323 (0.4); −0.0004 (0.9) 7-06: 1H-NMR(300.1 MHz, d6-DMSO): δ = 8.2155 (16.0); 7.7341 (7.2); 7.7275 (7.7); 7.5506 (3.7); 7.5436 (4.5); 7.5372 (4.2); 7.5236 (7.6); 7.5168 (5.3); 7.4449 (0.3); 7.4157 (0.4); 7.3984 (6.8); 7.3709 (4.8); 3.8599 (3.8); 3.8492 (2.5); 3.8298 (5.2); 3.8195 (3.2); 3.8003 (3.4); 3.7868 (3.4); 3.7610 (1.7); 3.7479 (0.8); 3.3219 (11.9); 3.0330 (0.6); 3.0099 (0.7); 2.9888 (3.5); 2.9737 (4.4); 2.9646 (4.0); 2.9539 (3.7); 2.9298 (0.7); 2.9071 (0.4); 2.5086 (8.0); 2.5028 (10.3); 2.4971 (7.5); −0.0005 (5.0) 7-07: 1H-NMR(499.9 MHz, CDCl3): δ = 7.7140 (16.0); 7.4065 (7.6); 7.4032 (7.7); 7.2656 (5.4); 7.2307 (1.6); 7.2271 (1.3); 7.2143 (8.0); 7.2106 (9.0); 7.2056 (11.5); 7.1892 (2.1); 5.4993 (3.4); 5.3006 (2.8); 4.0313 (0.4); 4.0240 (1.1); 4.0171 (1.8); 4.0099 (2.6); 4.0029 (2.8); 3.9958 (2.1); 3.9887 (1.7); 3.9841 (3.1); 3.9784 (1.7); 3.9618 (5.6); 3.9557 (4.4); 3.9353 (4.4); 3.9277 (3.9); 3.9130 (1.9); 3.9054 (1.6); 3.7266 (1.2); 3.7126 (3.6); 3.6986 (3.6); 3.6845 (1.2); 3.0865 (11.0); 3.0723 (10.4); 1.6189 (0.7); 1.2466 (4.2); 1.2325 (8.2); 1.2185 (4.1); −0.0002 (7.5) 7-08: 1H-NMR(499.9 MHz, CDCl3): δ = 7.7124 (16.0); 7.4052 (6.8); 7.4019 (7.1); 7.2660 (5.6); 7.2295 (1.4); 7.2259 (1.1); 7.2131 (7.5); 7.2094 (8.7); 7.2050 (11.2); 7.1886 (1.8); 5.5207 (3.3); 5.5152 (3.1); 5.3006 (2.8); 4.0308 (0.4); 4.0235 (1.0); 4.0166 (1.7); 4.0093 (2.4); 4.0024 (2.6); 3.9952 (2.0); 3.9883 (1.4); 3.9820 (2.9); 3.9762 (1.4); 3.9598 (5.4); 3.9536 (4.2); 3.9347 (4.4); 3.9270 (3.7); 3.9123 (1.8); 3.9047 (1.5); 3.7258 (1.3); 3.7118 (4.0); 3.6978 (4.0); 3.6837 (1.4); 3.0860 (10.7); 3.0718 (10.3); 1.6191 (0.5); 1.2542 (0.5); 1.2460 (4.6); 1.2320 (8.9); 1.2179 (4.4); −0.0002 (6.9); −0.0066 (0.4) 7-09: 1H-NMR(499.9 MHz, CDCl3): δ = 7.7134 (16.0); 7.5543 (7.9); 7.5505 (7.7); 7.3725 (4.0); 7.3686 (3.6); 7.3562 (4.6); 7.3524 (4.2); 7.2649 (5.7); 7.1463 (7.1); 7.1300 (6.1); 5.4857 (3.4); 5.3005 (0.5); 4.0322 (0.4); 4.0250 (1.1); 4.0180 (1.8); 4.0108 (2.6); 4.0038 (2.7); 3.9967 (2.1); 3.9898 (1.5); 3.9836 (3.0); 3.9778 (1.5); 3.9613 (5.6); 3.9553 (4.3); 3.9370 (4.6); 3.9293 (3.9); 3.9146 (1.8); 3.9069 (1.6); 3.4736 (3.7); 3.0745 (10.6); 3.0603 (10.0); 2.9415 (0.4); 2.8305 (0.3); 1.6217 (0.8); 1.2548 (0.4); 1.2471 (0.5); 1.2330 (0.8); 1.2190 (0.4); −0.0002 (7.5) 7-10: 1H-NMR(499.9 MHz, CDCl3): δ = 7.7114 (16.0); 7.5523 (7.6); 7.5485 (8.2); 7.3704 (3.8); 7.3666 (3.8); 7.3541 (4.4); 7.3503 (4.4); 7.2651 (5.4); 7.1454 (7.0); 7.1291 (6.1); 5.5112 (3.8); 5.5053 (3.6); 4.0314 (0.4); 4.0242 (1.1); 4.0172 (1.9); 4.0100 (2.7); 4.0031 (2.8); 3.9959 (2.1); 3.9891 (1.4); 3.9811 (2.8); 3.9750 (1.5); 3.9584 (5.7); 3.9524 (4.5); 3.9358 (4.8); 3.9282 (4.0); 3.9134 (1.8); 3.9058 (1.5); 3.4723 (4.3); 3.0738 (10.8); 3.0596 (10.4); 1.6192 (1.5); 1.2547 (0.5); 1.2464 (0.4); 1.2323 (0.6); −0.0002 (7.1) 7-11: 1H-NMR(499.9 MHz, CDCl3): δ = 7.7119 (8.6); 7.2611 (2.8); 7.0321 (2.0); 7.0168 (3.4); 7.0016 (3.3); 6.9848 (0.4); 6.9697 (2.2); 6.9560 (1.4); 5.2907 (1.8); 4.1155 (1.3); 4.1093 (1.5); 4.0938 (1.6); 4.0877 (1.8); 3.8916 (0.3); 3.8859 (0.6); 3.8806 (0.9); 3.8748 (1.0); 3.8691 (1.1); 3.8635 (1.0); 3.8582 (0.8); 3.8521 (0.7); 3.8467 (0.5); 3.8397 (2.3); 3.8289 (1.2); 3.8180 (1.8); 3.8072 (1.3); 2.9820 (1.0); 2.9700 (1.0); 2.9545 (1.5); 2.9422 (1.5); 2.8545 (1.5); 2.8379 (1.5); 2.8270 (1.1); 2.8101 (1.0); 2.3045 (16.0); 2.2828 (15.3); 1.6297 (0.9); 1.3879 (3.7); −0.0002 (3.7) 7-12: 1H-NMR(499.9 MHz, CDCl3): δ =7.7147 (8.0); 7.2607 (2.9); 7.0332 (2.2); 7.0179 (3.5); 7.0045 (3.1); 6.9744 (2.0); 6.9590 (1.2); 5.2531 (1.7); 4.1214 (1.4); 4.1152 (1.5); 4.0997 (1.6); 4.0935 (1.6); 3.8992 (0.3); 3.8930 (0.5); 3.8874 (0.7); 3.8820 (1.0); 3.8761 (1.1); 3.8705 (1.1); 3.8648 (1.1); 3.8594 (0.8); 3.8534 (0.7); 3.8479 (0.6); 3.8402 (2.2); 3.8293 (1.2); 3.8185 (1.7); 3.8076 (1.2); 2.9847 (1.1); 2.9727 (1.0); 2.9572 (1.5); 2.9449 (1.4); 2.8515 (1.6); 2.8347 (1.5); 2.8240 (1.1); 2.8069 (1.0); 2.3058 (16.0); 2.2846 (14.6); 1.5927 (1.7); −0.0002 (3.8)

TABLE 43 Compounds according to formula (8)

(8) Ex No A QS LogP 8-01 CH vinyl 1.96^([a]) 8-02 CH ethynyl 1.72^([a]) 8-03 CH cyclopropyl 2.12^([a]) 8-04 CH rac-2,2-difluorocyclopropyl 8-05 CH 1-fluorocyclopropyl

TABLE 44 8-01: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.2988 (8.3); 7.0822 (1.8); 7.0748 (2.4); 7.0563 (7.2); 7.0491 (7.3); 7.0406 (18.4); 7.0294 (8.8); 7.0183 (16.0); 7.0042 (0.7); 6.9921 (5.6); 6.9704 (6.4); 6.9630 (5.7); 6.9437 (7.8); 6.9375 (3.4); 6.9324 (4.6); 6.9257 (7.2); 6.9223 (4.7); 6.9109 (3.1); 6.8885 (6.8); 6.8667 (7.3); 6.8294 (7.6); 5.8978 (11.2); 5.8944 (11.6); 5.8387 (10.0); 5.8353 (10.3); 5.4557 (11.1); 5.4523 (11.2); 5.4184 (10.5); 5.4150 (10.7); 5.3378 (12.9); 5.2491 (9.5); 4.1831 (0.6); 4.1593 (0.6); 2.0946 (2.9); 1.6957 (8.4); 1.3266 (1.2); 1.3201 (1.8); 1.3029 (3.6); 1.2968 (3.9); 1.2790 (1.0); 1.2733 (1.4); 1.2639 (0.5); 0.9451 (0.6); 0.9234 (1.7); 0.9002 (0.7); 0.3136 (0.6); 0.3114 (0.6); 0.1135 (0.5); 0.0418 (9.8); 0.0309 (0.3) 8-02: ¹H-NMR(300.2 MHz, d₆-DMSO): δ = 10.1455 (8.9); 7.0552 (1.1); 7.0470 (1.7); 7.0289 (5.0); 7.0205 (9.8); 7.0119 (10.7); 6.9960 (16.0); 6.9699 (3.5); 6.9607 (5.1); 6.9527 (4.7); 6.9417 (4.7); 6.9369 (2.7); 6.9275 (4.1); 6.9101 (2.0); 5.7739 (1.2); 4.4408 (14.4); 3.3664 (6.0); 2.5345 (1.2); 2.5285 (2.7); 2.5225 (3.8); 2.5164 (2.8); 2.5105 (1.3); 1.2949 (0.5); 1.2576 (3.4); 1.0987 (1.2); 1.0754 (2.3); 1.0521 (1.1); 0.8946 (0.9); 0.8730 (3.1); 0.8497 (1.1); 0.0148 (5.1) 8-03: ¹H-NMR(300.1 MHz, d₆-DMSO): δ = 9.6264 (16.0); 6.8628 (2.1); 6.8591 (2.1); 6.8364 (5.2); 6.8326 (5.3); 6.8101 (3.6); 6.8066 (3.8); 6.7434 (3.5); 6.7378 (3.8); 6.7159 (5.1); 6.7104 (5.3); 6.6887 (2.4); 6.6832 (2.3); 6.3737 (2.6); 6.3684 (2.6); 6.3475 (4.7); 6.3262 (2.4); 6.3211 (2.2); 5.7578 (0.4); 4.0415 (0.8); 4.0178 (0.9); 3.3382 (6.7); 2.5154 (2.8); 2.5095 (5.4); 2.5036 (7.2); 2.4976 (4.9); 2.4918 (2.2); 2.0462 (0.7); 2.0289 (1.6); 2.0180 (1.8); 2.0009 (3.3); 1.9896 (5.1); 1.9730 (1.8); 1.9556 (0.9); 1.1988 (1.0); 1.1751 (2.1); 1.1513 (1.0); 0.9636 (2.7); 0.9495 (7.4); 0.9420 (7.8); 0.9356 (3.5); 0.9287 (4.0); 0.9210 (7.8); 0.9136 (7.1); 0.9005 (3.3); 0.8787 (0.4); 0.7131 (0.3); 0.6811 (3.5); 0.6678 (8.1); 0.6606 (8.4); 0.6506 (7.8); 0.6434 (8.0); 0.6289 (2.6); −0.0004 (5.8) 8-04: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.2988 (0.5); 7.0418 (0.4); 7.0149 (1.2); 6.9891 (2.4); 6.9810 (1.1); 6.9623 (0.9); 6.9569 (0.9); 6.9354 (0.3); 6.7340 (0.4); 6.7264 (0.4); 6.7100 (0.8); 6.6868 (0.4); 6.6841 (0.4); 5.4977 (1.0); 5.3330 (0.8); 2.8803 (0.3); 2.8674 (0.6); 2.8398 (0.6); 2.8264 (0.4); 2.7988 (0.3); 2.0439 (16.0); 1.9405 (0.4); 1.9265 (0.6); 1.9103 (0.5); 1.9009 (0.6); 1.8842 (0.6); 1.8612 (0.4); 1.8442 (0.4); 1.7154 (0.3); 1.7014 (0.5); 1.6880 (0.7); 1.6738 (0.5); 1.6597 (0.7); 1.6462 (0.6); 0.0359 (0.7) 8-05: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.2989 (22.6); 7.1680 (0.4); 7.1558 (0.6); 7.1500 (0.9); 7.1325 (1.2); 7.1213 (0.4); 7.1047 (1.8); 7.0896 (1.0); 7.0770 (4.3); 7.0605 (33.6); 7.0549 (23.8); 7.0432 (11.9); 7.0398 (16.0); 7.0347 (9.4); 7.0256 (4.5); 7.0210 (3.8); 7.0125 (2.1); 7.0074 (1.9); 7.0039 (1.9); 5.1920 (11.4); 3.6842 (0.4); 3.3468 (0.4); 2.1527 (0.4); 2.1394 (0.3); 2.1195 (0.3); 2.1161 (0.3); 2.0859 (0.3); 2.0500 (0.4); 1.6703 (0.4); 1.6596 (0.6); 1.6394 (7.8); 1.5230 (3.1); 1.5003 (9.4); 1.4973 (10.4); 1.4743 (4.2); 1.4603 (3.2); 1.4377 (9.4); 1.4345 (10.3); 1.4116 (4.9); 1.3500 (0.5); 1.2497 (0.7); 1.2391 (0.5); 1.2200 (0.8); 1.1889 (4.2); 1.1732 (5.5); 1.1681 (11.0); 1.1612 (12.7); 1.1386 (13.2); 1.1327 (9.8); 1.1110 (3.1); 0.0502 (0.9); 0.0394 (29.9); 0.0285 (1.1)

TABLE 15 Compounds according to formula (9)

Ex No R⁷ R⁸ Q LogP 9-01 Cl H 3-cyclopropylphenyl 3.37^([a]) 9-02 CH₃ H 3-(trifluoromethyl)phenyl 2.84^([a]) 9-03 Cl H 3-(trifluoromethyl)phenyl 3.25^([a]) 9-04 Cl H 3-cyclopropyl-2-fluorophenyl 3.54^([a]) 9-05 Cl H 3-bromo-2-fluorophenyl 3.28^([a]) 9-06 Cl H 3-chloro-2-fluorophenyl 3.23^([a]) 9-07 Cl H 3-chlorophenyl 3.14^([a]) 9-08 Cl H 3-methoxyphenyl 2.75^([a]) 9-09 Cl H 3-(difluoromethyl)-2-fluorophenyl 3.00^([a])

TABLE 16 9-01: ¹H-NMR(300.2 MHz, d₆-DMSO): δ = 8.8636 (0.4); 8.7495 (0.4); 8.7364 (8.6); 8.4333 (0.4); 7.4065 (1.6); 7.3804 (3.7); 7.3543 (2.6); 7.1249 (2.0); 7.1174 (2.3); 7.0975 (4.0); 7.0683 (5.1); 7.0618 (3.7); 3.3454 (16.0); 2.5285 (3.7); 2.5226 (5.0); 2.5167 (3.6); 2.0302 (0.4); 2.0131 (1.0); 2.0022 (1.1); 1.9856 (1.9); 1.9689 (1.1); 1.9578 (1.1); 1.9411 (0.5); 1.0323 (1.2); 1.0176 (3.3); 1.0102 (3.7); 0.9965 (1.9); 0.9897 (3.5); 0.9824 (3.3); 0.9689 (1.4); 0.7438 (1.4); 0.7298 (3.8); 0.7230 (4.0); 0.7135 (3.7); 0.7066 (4.1); 0.6913 (1.1); 0.0207 (3.9) 9-02: ¹H-NMR(499.9 MHz, d₆-DMSO): δ = 8.3226 (5.8); 7.8030 (2.1); 7.7645 (0.5); 7.7488 (1.7); 7.7330 (1.7); 7.7108 (1.8); 7.6949 (1.0); 7.6900 (1.4); 7.6870 (1.4); 7.6711 (0.8); 3.3405 (9.8); 2.6232 (16.0); 2.5124 (1.0); 2.5089 (2.1); 2.5053 (2.9); 2.5018 (2.2); 2.4984 (1.1) 9-03: 1H-NMR(499.9 MHz, CDCl3): δ = 7.8051 (16.0); 7.7925 (0.5); 7.6282 (0.7); 7.6123 (4.7); 7.6047 (4.6); 7.6008 (11.6); 7.5994 (11.9); 7.5751 (0.4); 7.5593 (5.7); 7.5460 (0.6); 7.5055 (0.5); 7.5014 (0.5); 7.4962 (2.1); 7.4897 (3.3); 7.4855 (3.2); 7.4780 (2.6); 7.4732 (1.7); 7.2595 (5.8); 4.1272 (0.3); 4.1129 (0.3); 2.0409 (1.4); 1.5504 (11.9); 1.2892 (0.4); 1.2712 (0.9); 1.2659 (1.2); 1.2572 (1.3); 1.2429 (0.6); 0.8953 (0.7); 0.8817 (1.8); 0.8675 (0.9); −0.0002 (4.6) 9-04: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.8211 (16.0); 7.5866 (0.7); 7.2986 (19.8); 7.1715 (0.7); 7.1570 (0.5); 7.1443 (8.9); 7.1296 (5.4); 7.1264 (6.9); 7.1215 (4.7); 7.1169 (4.3); 7.0990 (1.1); 7.0899 (0.4); 6.9111 (1.7); 6.8941 (2.4); 6.8893 (2.0); 6.8796 (2.8); 6.8664 (1.6); 6.8573 (1.4); 2.1713 (0.6); 2.1541 (1.2); 2.1429 (1.3); 2.1257 (2.4); 2.1083 (1.4); 2.0975 (1.3); 2.0802 (0.7); 1.5885 (9.5); 1.2911 (1.0); 1.0918 (1.8); 1.0765 (4.7); 1.0697 (5.0); 1.0637 (2.5); 1.0547 (2.7); 1.0478 (4.9); 1.0414 (4.4); 1.0265 (2.2); 1.0049 (0.3); 0.8975 (0.4); 0.8794 (0.6); 0.8615 (0.4); 0.8294 (2.4); 0.8143 (5.5); 0.8082 (5.2); 0.7973 (4.8); 0.7919 (5.8); 0.7752 (1.7); 0.1071 (6.8); 0.0482 (1.0); 0.0465 (0.6); 0.0374 (26.7); 0.0280 (1.0); 0.0265 (1.2) 9-05: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.8483 (16.0); 7.6320 (0.6); 7.6035 (1.9); 7.5983 (2.1); 7.5835 (2.1); 7.5776 (3.4); 7.5712 (2.4); 7.5564 (2.3); 7.5510 (2.4); 7.3553 (1.7); 7.3501 (1.8); 7.3330 (1.9); 7.3279 (4.2); 7.3227 (2.6); 7.3054 (3.4); 7.2987 (23.6); 7.2069 (2.8); 7.2015 (2.7); 7.1796 (4.2); 7.1742 (4.2); 7.1523 (1.7); 7.1469 (1.8); 5.3383 (0.4); 2.0467 (0.6); 1.5894 (7.8); 1.3214 (0.3); 1.2924 (1.1); 0.8972 (0.6); 0.8770 (0.7); 0.1066 (0.6); 0.0479 (0.5); 0.0371 (30.2); 0.0263 (1.8) 9-06: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.8612 (0.3); 7.8506 (16.0); 7.6349 (0.8); 7.4606 (1.7); 7.4545 (1.8); 7.4390 (1.9); 7.4336 (3.1); 7.4279 (2.5); 7.4136 (2.1); 7.4064 (2.4); 7.3149 (1.3); 7.3088 (1.6); 7.2987 (18.4); 7.2874 (4.3); 7.2812 (2.7); 7.2672 (3.6); 7.2600 (2.8); 7.2509 (4.1); 7.2471 (3.6); 7.2253 (3.7); 7.2202 (3.8); 7.1978 (1.2); 7.1928 (1.3); 5.3383 (0.4); 1.5935 (2.8); 1.3708 (0.4); 1.2919 (2.4); 1.2543 (0.4); 0.9173 (0.4); 0.8981 (0.9); 0.8773 (1.1); 0.1068 (1.2); 0.0479 (0.5); 0.0370 (24.2); 0.0263 (1.2) 9-07: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.8274 (16.0); 7.5440 (0.3); 7.4731 (2.2); 7.4652 (0.6); 7.4521 (0.8); 7.4445 (5.0); 7.4222 (1.7); 7.4173 (4.1); 7.3734 (2.1); 7.3673 (4.1); 7.3636 (4.1); 7.3525 (3.4); 7.3451 (8.3); 7.3399 (8.1); 7.2990 (12.4); 7.2359 (2.8); 7.2323 (3.0); 7.2283 (2.8); 7.2247 (2.6); 7.2091 (2.2); 7.2028 (2.7); 7.1976 (2.0); 1.5900 (5.7); 1.2927 (0.5); 0.0485 (0.5); 0.0376 (16.9); 0.0267 (0.7) 9-08: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.8019 (5.3); 7.4234 (1.0); 7.3960 (2.2); 7.3687 (1.3); 7.2987 (4.8); 6.9231 (0.8); 6.9207 (0.9); 6.9152 (1.0); 6.9128 (1.0); 6.8956 (1.5); 6.8929 (1.5); 6.8880 (2.0); 6.8854 (1.7); 6.8689 (0.6); 6.8661 (0.7); 6.8615 (1.2); 6.8587 (0.9); 6.8445 (1.6); 6.8370 (2.1); 6.8294 (0.9); 3.8603 (16.0); 1.5917 (2.5); 0.0375 (6.6) 9-09: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.8680 (0.3); 7.8574 (16.0); 7.6502 (2.0); 7.6241 (2.3); 7.6015 (1.5); 7.5329 (1.0); 7.5302 (1.0); 7.5086 (2.4); 7.5059 (2.4); 7.4846 (1.8); 7.4819 (1.7); 7.4791 (1.5); 7.4205 (2.2); 7.3927 (3.0); 7.3653 (1.3); 7.2988 (20.2); 7.1180 (2.6); 6.9358 (5.1); 6.7537 (2.6); 1.5905 (3.2); 1.2925 (1.2); 0.8974 (0.6); 0.8773 (0.8); 0.1070 (0.5); 0.0481 (0.6); 0.0373 (28.1); 0.0264 (1.5)

TABLE 17 Compounds according to formula (10)

Ex No R⁷ R⁸ Q LogP 10-01 Cl H 3-(trifluoromethyl)phenyl 2.18^([a]) 10-02 CH₃ H 3-(trifluoromethyl)phenyl 1.69^([a]) 10-03 Cl H 3-methoxyphenyl 1.59^([a]) 10-04 Cl H 3-chlorophenyl 2.00^([a]) 10-05 Cl H 3-bromo-2-fluorophenyl 2.21^([a]) 10-06 Cl H 3-chloro-2-fluorophenyl 2.12^([a]) 10-07 Cl H 3-cyclopropyl-2-fluorophenyl 2.34^([a]) 10-08 Cl H 3-cyclopropylphenyl 2.19^([a]) 10-09 Cl H 3-(difluoromethyl)-2-fluorophenyl 1.91^([a]) 10-01 Cl H 3-(trifluoromethyl)phenyl 2.18^([a])

TABLE 18 10-01: 1H-NMR(300.2 MHz, d6-DMSO): δ = 10.2733 (5.4); 8.0186 (5.3); 7.7748 (1.5); 7.7413 (1.1); 7.7155 (1.4); 7.6965 (1.5); 7.6706 (0.6); 7.6530 (1.1); 7.6271 (0.6); 6.1846 (2.2); 3.3428 (16.0); 2.5343 (1.0); 2.5284 (2.0); 2.5223 (2.7); 2.5163 (2.0); 2.5104 (0.9); 1.2674 (0.7); 0.8788 (0.7); 0.0204 (1.5) 10-02: 1H-NMR(499.9 MHz, CDCl3): δ = 7.7682 (5.0); 7.7215 (0.9); 7.5696 (0.5); 7.5541 (1.5); 7.5386 (1.9); 7.5317 (1.9); 7.5161 (0.6); 7.4900 (1.8); 7.4271 (0.9); 7.4239 (1.2); 7.4203 (0.8); 7.4085 (0.9); 7.2612 (3.8); 5.5062 (1.6); 2.7415 (0.6); 2.6724 (16.0); 2.0465 (1.1); 1.6500 (0.5); 1.2593 (0.6); - 0.0002 (3.9) 10-03: 1H-NMR(300.2 MHz, CDCl3): δ = 7.9700 (5.3); 7.8904 (0.6); 7.4004 (1.2); 7.3734 (2.3); 7.3460 (1.4); 7.2992 (2.0); 6.8900 (1.1); 6.8826 (1.2); 6.8616 (1.0); 6.8562 (1.1); 6.8382 (1.2); 6.8326 (1.4); 6.8020 (2.6); 6.7936 (2.5); 6.7865 (1.0); 5.6142 (2.0); 5.3362 (1.5); 3.8566 (1.5); 3.8453 (16.0); 1.7378 (0.5); 0.1086 (0.7); 0.0373 (2.5) 10-07: 1H-NMR(300.2 MHz, CDCl3): δ = 8.3416 (0.4); 7.9757 (16.0); 7.5480 (1.0); 7.4814 (0.3); 7.2990 (10.6); 7.1786 (0.6); 7.1711 (1.0); 7.1641 (0.4); 7.1518 (3.6); 7.1438 (6.0); 7.1384 (7.2); 7.1242 (4.2); 7.1199 (6.7); 7.0926 (1.3); 6.8834 (1.8); 6.8758 (1.8); 6.8602 (2.8); 6.8510 (1.8); 6.8444 (2.0); 6.8294 (1.3); 5.6089 (3.9); 5.3373 (1.6); 2.1656 (0.6); 2.1482 (1.2); 2.1372 (1.3); 2.1200 (2.4); 2.1027 (1.4); 2.0918 (1.3); 2.0743 (0.7); 1.6747 (1.7); 1.5523 (0.5); 1.2925 (1.0); 1.0807 (1.8); 1.0653 (4.5); 1.0585 (5.0); 1.0528 (2.7); 1.0438 (2.7); 1.0367 (4.9); 1.0302 (4.5); 1.0155 (2.2); 0.8718 (0.4); 0.8219 (2.3); 0.8068 (5.4); 0.8007 (5.4); 0.7899 (4.8); 0.7841 (5.8); 0.7677 (1.7); 0.1078 (4.1); 0.0481 (0.4); 0.0371 (12.8); 0.0262 (0.5) 10-08: 1H-NMR(300.2 MHz, d6-DMSO): δ = 10.2338 (5.4); 7.9672 (5.9); 7.3559 (0.9); 7.3298 (1.8); 7.3038 (1.2); 7.0338 (1.6); 7.0267 (2.7); 7.0066 (1.4); 7.0000 (3.0); 6.9839 (1.8); 6.9778 (2.0); 6.9717 (1.0); 6.1422 (2.4); 4.0838 (1.2); 4.0601 (3.5); 4.0364 (3.6); 4.0127 (1.2); 3.3534 (16.0); 2.5338 (1.6); 2.5279 (3.2); 2.5218 (4.3); 2.5158 (3.1); 2.5099 (1.5); 2.0092 (15.8); 1.9907 (0.6); 1.9792 (0.6); 1.9627 (1.0); 1.9458 (0.6); 1.9348 (0.5); 1.2177 (4.3); 1.1940 (8.6); 1.1703 (4.2); 1.0158 (0.6); 1.0013 (1.7); 0.9938 (1.8); 0.9883 (1.0); 0.9803 (1.1); 0.9733 (1.8); 0.9659 (1.6); 0.9526 (0.7); 0.9040 (0.3); 0.7246 (0.8); 0.7109 (1.9); 0.7039 (1.9); 0.6943 (1.8); 0.6874 (1.9); 0.6724 (0.6); 0.0195 (3.6) 10-09: 1H-NMR(300.2 MHz, CDCl3): δ = 8.3615 (0.4); 7.9923 (16.0); 7.6200 (2.6); 7.6096 (2.6); 7.5837 (3.0); 7.5607 (2.0); 7.5368 (1.9); 7.5113 (3.2); 7.4869 (2.0); 7.3976 (2.8); 7.3704 (3.8); 7.3432 (1.5); 7.2989 (8.7); 7.1114 (3.0); 6.9290 (6.1); 6.7467 (3.0); 5.5443 (4.3); 5.3371 (2.9); 1.6823 (2.5); 1.2920 (0.5); 0.1076 (0.9); 0.0473 (0.3); 0.0366 (10.8); 0.0258 (0.5)

TABLE 19 Compounds according to formula (12)

Ex No R⁷ R⁸ Q

L—R⁶ LogP 12-01 CH₃ H 3-(trifluoro- methyl)phenyl

4-methoxyphenyl 3.00^([a]) 12-02 CH₃ H 3-(trifluoro- methyl)phenyl

phenyl 3.04^([a]) 12-03 CH₃ H 3-(trifluoro- methyl)phenyl

4-chlorophenyl 3.42^([a]) 12-04 CH₃ H 3-(trifluoro- methyl)phenyl

3,4-dimethylphenyl 3.60^([a]) 12-05 CH₃ H 3-(trifluoro- methyl)phenyl

1-methyl-1H-indol-3-yl 3.00^([a]) 12-06 CH₃ H 3-(trifluoro- methyl)phenyl

4-chlorophenyl 3.35 & 3.79^([a]) 12-07 CH₃ H 3-(trifluoro- methyl)phenyl

2,3-dihydro-1- benzofuran-5-yl 3.00^([a]) 12-08 CH₃ H 3-(trifluoro- methyl)phenyl

2-(4-chloro-2,6- difluorophenyl)ethyl 3.42 & 4.03^([a]) 12-09 CH₃ H 3-(trifluoro- methyl)phenyl

2,4-difluorophenyl 3.88^([a]) 12-10 CH₃ H 3-(trifluoro- methyl)phenyl

2,4-dichlorophenyl 4.06 & 4.49^([a]) 12-11 CH₃ H 3-(trifluoro- methyl)phenyl

2-(4-chlorophenyl)ethyl 3.19^([a]) 12-12 CH₃ H 3-(trifluoro- methyl)phenyl

3,4-dichlorophenyl 4.59^([a]) 12-13 CH₃ H 3-(trifluoro- methyl)phenyl

4-chlorophenyl 3.19^([a]) 12-14 CH₃ H 3-(trifluoro- methyl)phenyl

4-methoxyphenyl 3.13^([a]) 12-15 CH₃ H 3-(trifluoro- methyl)phenyl

2-phenylcyclopropyl 3.57^([a]) 12-16 CH₃ H 3-(trifluoro- methyl)phenyl

2,3-dihydro-1,4-benzo- dioxin-6-yl 3.07^([a]) In table 19, ″#″ denotes the point of attachment to the L—R⁶ group and ″*″ denotes the point of attachment to the pyridazin-4-yl group.

TABLE 20 12-02: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1719 (0.8); 8.0856 (0.3); 8.0280 (2.6); 8.0044 (3.2); 7.9996 (2.5); 7.9595 (0.4); 7.9386 (0.4); 7.9154 (0.4); 7.8590 (0.5); 7.8431 (0.5); 7.8347 (0.6); 7.8300 (0.5); 7.8114 (5.0); 7.7793 (0.6); 7.7553 (0.6); 7.7513 (0.6); 7.7031 (1.0); 7.6761 (1.3); 7.6591 (0.9); 7.6518 (2.0); 7.6447 (1.1); 7.6316 (1.4); 7.6269 (1.9); 7.6222 (1.7); 7.6095 (1.1); 7.5971 (2.3); 7.5871 (1.4); 7.5711 (4.7); 7.5655 (4.3); 7.5381 (4.1); 7.5203 (2.8); 7.5143 (2.7); 7.4913 (1.3); 7.4823 (1.3); 7.4697 (2.1); 7.4612 (2.2); 7.4542 (1.7); 7.4381 (1.6); 7.4087 (0.5); 7.3699 (0.6); 7.3434 (0.7); 7.3182 (0.5); 7.2987 (25.4); 5.8101 (0.6); 5.7328 (1.7); 5.4210 (10.8); 5.3829 (0.4); 5.3375 (7.1); 3.9859 (0.3); 2.7983 (0.5); 2.7516 (0.8); 2.7265 (1.9); 2.7090 (0.5); 2.6908 (2.5); 2.6728 (16.0); 1.6253 (0.5); 1.2932 (0.8); 0.1083 (0.7); 0.0492 (1.0); 0.0384 (27.6); 0.0277 (1.1) 12-03: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9778 (4.0); 7.9714 (1.4); 7.9552 (1.6); 7.9490 (4.4); 7.9410 (0.7); 7.7872 (5.1); 7.6443 (0.3); 7.6225 (0.6); 7.5959 (1.6); 7.5722 (4.1); 7.5476 (0.8); 7.5251 (6.0); 7.5187 (3.4); 7.5025 (1.8); 7.4964 (4.1); 7.4620 (1.1); 7.4540 (1.7); 7.4467 (1.0); 7.4372 (0.9); 7.4315 (1.2); 7.4142 (0.4); 7.2984 (16.0); 5.7581 (0.3); 5.7160 (1.9); 5.3565 (11.0); 5.3370 (8.4); 2.7744 (0.4); 2.7492 (0.6); 2.7019 (0.7); 2.6727 (16.0); 2.0823 (0.3); 1.6105 (1.4); 1.2963 (0.8); 0.9198 (0.4); 0.0483 (0.8); 0.0377 (16.4); 0.0267 (0.6) 12-04: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.8196 (3.4); 7.7834 (1.8); 7.7570 (1.0); 7.7309 (1.0); 7.5940 (1.0); 7.5691 (2.9); 7.5439 (0.5); 7.5239 (1.5); 7.4670 (0.7); 7.4594 (1.0); 7.4526 (0.6); 7.4362 (0.7); 7.2984 (4.8); 7.2663 (1.3); 5.7438 (1.6); 5.3956 (6.8); 4.1939 (0.4); 4.1701 (1.1); 4.1464 (1.1); 4.1227 (0.4); 2.6685 (10.4); 2.3923 (0.5); 2.3680 (16.0); 2.3455 (1.0); 2.2569 (0.4); 2.1591 (0.4); 2.0821 (5.0); 1.6509 (1.4); 1.3196 (1.3); 1.2958 (2.7); 1.2720 (1.2); 0.1075 (1.6); 0.0377 (5.4); 0.0365 (5.8) 12-05: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.4050 (1.0); 8.4035 (1.1); 8.3969 (0.7); 8.3915 (1.1); 8.3869 (1.0); 8.0076 (0.5); 7.9742 (0.6); 7.8914 (4.7); 7.7961 (5.1); 7.6517 (0.6); 7.5515 (0.4); 7.5361 (1.4); 7.5211 (2.9); 7.5035 (0.5); 7.4816 (2.0); 7.4719 (0.5); 7.4701 (0.5); 7.4087 (0.8); 7.4047 (1.3); 7.4005 (0.8); 7.3901 (0.9); 7.3862 (0.6); 7.3762 (0.3); 7.3748 (0.3); 7.3693 (0.6); 7.3642 (0.8); 7.3594 (2.0); 7.3561 (3.1); 7.3512 (1.1); 7.3473 (2.4); 7.3431 (2.8); 7.3348 (1.6); 7.3281 (2.1); 7.3231 (1.1); 7.3194 (0.3); 7.3153 (0.6); 7.3105 (0.7); 7.2839 (0.4); 7.2594 (5.6); 7.0776 (0.5); 5.7284 (2.1); 5.1739 (10.2); 3.8656 (0.5); 3.8514 (16.0); 3.7950 (0.6); 3.7721 (1.3); 3.7371 (2.0); 3.3521 (0.7); 3.3351 (0.4); 2.9475 (3.9); 2.8759 (3.4); 2.7301 (0.4); 2.6900 (1.9); 2.6113 (15.7); 2.0415 (1.0); 1.6621 (2.3); 1.2568 (0.5); −0.0002 (5.6) 12-06: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1894 (0.4); 8.0615 (1.4); 8.0491 (2.3); 8.0333 (1.8); 8.0201 (4.2); 8.0036 (1.6); 7.9914 (2.2); 7.9779 (0.7); 7.9589 (3.5); 7.9383 (0.8); 7.9286 (1.3); 7.9002 (0.4); 7.6900 (2.5); 7.6454 (0.5); 7.6171 (1.0); 7.5725 (6.2); 7.5444 (5.2); 7.5250 (2.6); 7.5170 (3.3); 7.5083 (3.1); 7.5015 (4.4); 7.4958 (4.3); 7.4888 (3.7); 7.4787 (3.8); 7.4728 (4.0); 7.4561 (1.8); 7.4427 (1.4); 7.4231 (1.9); 7.4157 (2.2); 7.4019 (5.2); 7.3730 (3.4); 7.3324 (0.5); 7.2996 (27.1); 7.2505 (0.6); 7.2261 (0.5); 7.1571 (0.6); 7.0382 (0.4); 6.9101 (0.6); 6.7943 (1.2); 5.6440 (1.2); 5.5646 (0.4); 5.5417 (1.1); 5.5187 (1.2); 5.4961 (0.6); 5.4794 (0.6); 5.4572 (0.6); 5.3381 (0.4); 5.2734 (0.7); 5.2511 (0.8); 5.2286 (0.9); 5.2064 (0.7); 4.2017 (0.4); 4.1934 (0.8); 4.1796 (0.5); 4.1697 (2.1); 4.1460 (2.1); 4.1220 (0.8); 3.8602 (1.1); 3.8392 (1.1); 3.8176 (0.3); 3.7251 (0.4); 3.3231 (0.5); 3.3077 (0.4); 3.2934 (1.2); 3.2839 (1.0); 3.2698 (1.6); 3.2566 (1.7); 3.2439 (1.5); 3.2334 (2.3); 3.2097 (0.5); 3.0283 (0.9); 3.0042 (0.9); 2.8353 (5.0); 2.8015 (5.5); 2.7751 (1.8); 2.7433 (12.9); 2.6817 (0.5); 2.6513 (8.0); 2.6119 (0.9); 2.0822 (9.7); 2.0452 (0.4); 1.9517 (2.8); 1.9297 (2.7); 1.7936 (3.0); 1.7786 (2.8); 1.7716 (3.6); 1.7557 (2.5); 1.7279 (0.4); 1.7025 (0.4); 1.6650 (4.0); 1.6419 (4.2); 1.6157 (16.0); 1.5688 (0.5); 1.5500 (0.3); 1.4934 (1.0); 1.4625 (10.9); 1.4374 (1.0); 1.4142 (0.9); 1.3202 (2.6); 1.2964 (5.3); 1.2850 (1.4); 1.2726 (2.7); 1.2595 (3.6); 1.2352 (5.1); 1.2114 (6.4); 1.1905 (4.3); 1.1138 (0.4); 1.0836 (1.8); 1.0618 (1.7); 0.1071 (1.3); 0.0479 (1.4); 0.0371 (34.0) 12-07: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.6214 (0.3); 8.1868 (0.4); 7.9076 (1.7); 7.8686 (1.0); 7.8630 (0.9); 7.8407 (1.2); 7.8239 (3.3); 7.6164 (0.8); 7.5932 (1.4); 7.5857 (1.0); 7.5682 (2.5); 7.5432 (0.7); 7.5217 (1.3); 7.4933 (0.4); 7.4658 (0.7); 7.4584 (1.1); 7.4519 (0.7); 7.4347 (0.7); 7.2987 (14.2); 6.8835 (2.1); 6.8556 (2.0); 6.3723 (0.3); 5.7407 (1.2); 5.3717 (0.8); 5.3555 (5.9); 5.3366 (16.0); 5.2948 (0.9); 4.7521 (1.2); 4.7431 (1.8); 4.7232 (2.3); 4.7139 (3.4); 4.6935 (1.6); 4.6846 (2.1); 4.6740 (2.9); 4.6620 (0.5); 3.3341 (1.5); 3.3051 (2.9); 3.2755 (1.9); 3.2617 (0.8); 3.2377 (0.5); 3.2225 (0.4); 2.9866 (0.9); 2.8389 (0.8); 2.8049 (0.9); 2.7902 (0.8); 2.7740 (1.4); 2.7568 (0.3); 2.7423 (0.4); 2.7129 (0.4); 2.6926 (0.6); 2.6691 (9.1); 2.0822 (0.9); 1.6578 (2.5); 1.4680 (1.6); 1.4658 (1.6); 1.2957 (0.6); 1.2635 (0.4); 1.2397 (0.7); 1.2160 (0.3); 0.1062 (5.2); 0.0470 (0.7); 0.0361 (18.0); 0.0254 (0.8) 12-09: ¹H-NMR(499.9 MHz, CDCl3): δ = 7.6446 (0.3); 7.6283 (0.7); 7.6148 (0.6); 7.6122 (0.6); 7.5986 (0.4); 7.5453 (0.9); 7.5299 (1.9); 7.5126 (0.3); 7.4418 (3.0); 7.4222 (1.3); 7.3556 (0.8); 7.3520 (0.5); 7.3409 (0.6); 7.2607 (4.0); 6.8640 (0.4); 6.8520 (0.6); 6.8474 (0.7); 6.8322 (0.7); 6.8147 (0.5); 6.8118 (0.7); 6.8077 (0.5); 6.7944 (0.4); 6.7897 (0.4); 5.4371 (1.5); 2.6997 (0.4); 2.6145 (9.2); 1.6786 (16.0); 1.5624 (3.6); 1.2548 (0.6); 0.0701 (0.9); −0.0002 (4.5) 12-10: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.0836 (0.9); 8.0419 (0.5); 8.0131 (0.5); 7.7172 (2.2); 7.6770 (0.4); 7.6492 (0.6); 7.6349 (0.4); 7.6139 (0.8); 7.5921 (0.8); 7.5679 (2.0); 7.5496 (1.3); 7.5439 (1.3); 7.5281 (1.3); 7.5160 (1.1); 7.5005 (2.6); 7.4960 (2.0); 7.4894 (2.3); 7.4816 (2.8); 7.4745 (1.9); 7.4580 (0.9); 7.4506 (1.1); 7.4419 (1.1); 7.4320 (0.9); 7.4246 (0.5); 7.4079 (1.0); 7.3982 (0.9); 7.3918 (1.2); 7.3865 (1.1); 7.3806 (1.1); 7.3637 (1.1); 7.3544 (0.6); 7.3412 (1.1); 7.3347 (1.0); 7.3134 (0.8); 7.3066 (1.0); 7.2988 (18.8); 7.2731 (0.4); 7.1033 (0.4); 5.5598 (1.0); 5.3376 (16.0); 5.2373 (0.5); 5.2216 (0.5); 5.2102 (0.6); 5.1942 (0.5); 5.0645 (0.3); 5.0584 (0.4); 5.0381 (0.4); 3.2934 (0.6); 3.2793 (0.4); 3.2694 (0.6); 3.2559 (0.7); 3.2317 (0.5); 3.0234 (0.7); 2.9993 (0.7); 2.8402 (2.3); 2.8149 (1.2); 2.8063 (2.7); 2.7763 (1.3); 2.7429 (0.4); 2.7265 (2.9); 2.6994 (0.7); 2.6836 (6.8); 2.1479 (0.5); 2.1233 (0.6); 2.1069 (0.4); 2.0995 (0.6); 2.0839 (0.5); 2.0755 (0.6); 2.0595 (0.6); 2.0376 (0.6); 2.0271 (0.4); 2.0134 (0.7); 2.0060 (0.5); 1.9882 (0.6); 1.9822 (0.4); 1.9649 (0.4); 1.6705 (0.3); 1.4633 (4.5); 1.3466 (0.3); 1.3383 (0.4); 1.3043 (0.5); 1.2847 (1.2); 1.2732 (1.2); 1.2606 (1.6); 1.2495 (2.1); 1.2364 (0.9); 1.2254 (1.1); 1.1973 (0.7); 1.1796 (1.1); 1.1616 (2.4); 1.1554 (2.5); 1.1371 (4.8); 1.1271 (1.7); 1.1125 (2.2); 1.1025 (0.8); 1.0399 (0.8); 1.0152 (1.4); 0.9905 (0.7); 0.1066 (3.4); 0.0476 (0.6); 0.0369 (22.3); 0.0261 (1.1) 12-11: ¹H-NMR(400.1 MHz, d₆-DMSO): δ = 7.9907 (3.5); 7.7237 (3.5); 7.7109 (6.1); 7.6847 (2.3); 7.6651 (2.2); 7.6298 (2.7); 7.6089 (3.3); 7.5865 (1.3); 7.2503 (4.3); 7.2299 (5.7); 7.1867 (0.4); 7.1769 (0.4); 7.1065 (5.3); 7.0860 (3.9); 5.9670 (5.1); 3.7999 (2.0); 3.7727 (2.6); 3.6163 (2.8); 3.5884 (2.2); 3.4305 (0.4); 3.3130 (289.4); 2.6897 (2.0); 2.6749 (2.4); 2.6016 (16.0); 2.5009 (57.6); 2.3256 (0.4); 2.0835 (0.4); 1.9868 (0.4); 1.8835 (2.1); 1.8677 (2.0); 1.8512 (1.1); −0.0002 (14.4) 12-15: 1H-NMR(300.2 MHz, CDCl3): δ = 7.6709 (5.0); 7.6227 (0.3); 7.5970 (1.3); 7.5740 (3.9); 7.5515 (0.4); 7.4943 (1.8); 7.4442 (0.7); 7.4356 (1.3); 7.4283 (0.8); 7.4231 (0.5); 7.4197 (0.5); 7.4137 (0.8); 7.4059 (0.5); 7.2987 (15.0); 7.2780 (0.6); 7.2718 (0.8); 7.2661 (0.4); 7.2495 (2.5); 7.2442 (1.3); 7.2254 (3.0); 7.2162 (1.1); 7.2102 (1.7); 7.2048 (1.1); 7.1965 (0.5); 7.1878 (1.3); 7.1630 (0.4); 7.1237 (2.4); 7.1180 (2.9); 7.0959 (2.1); 5.6457 (2.0); 5.3379 (9.7); 4.8253 (6.6); 4.8221 (6.4); 2.6511 (16.0); 2.6277 (0.6); 2.6190 (0.6); 2.6103 (0.6); 2.6058 (0.7); 2.5978 (0.7); 2.5890 (0.5); 2.5756 (0.6); 2.5478 (0.7); 2.5341 (0.7); 2.5297 (1.0); 2.5209 (0.9); 2.5164 (0.7); 2.5074 (0.8); 2.5029 (0.9); 2.4894 (0.6); 2.0837 (0.7); 1.8899 (0.7); 1.8759 (0.9); 1.8719 (0.8); 1.8594 (1.2); 1.8460 (0.8); 1.8419 (0.8); 1.8281 (0.6); 1.6017 (10.5); 1.5040 (0.7); 1.4902 (0.8); 1.4818 (0.8); 1.4771 (0.9); 1.4680 (0.8); 1.4635 (0.8); 1.4550 (0.8); 1.4413 (0.6); 1.3215 (0.3); 1.2974 (0.7); 0.1074 (4.3); 0.0484 (0.7); 0.0377 (20.6); 0.0283 (0.6); 0.0268 (0.7) 12-16: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.9519 (0.5); 7.8240 (3.6); 7.6362 (0.7); 7.6207 (0.9); 7.5962 (1.4); 7.5694 (7.8); 7.5433 (2.0); 7.5361 (1.6); 7.5234 (1.8); 7.4812 (0.4); 7.4670 (0.9); 7.4591 (1.3); 7.4521 (0.8); 7.4361 (1.0); 7.2985 (18.9); 6.9890 (1.6); 6.9629 (1.5); 6.9433 (0.4); 5.7332 (1.8); 5.7051 (1.1); 5.3385 (11.1); 4.3764 (2.2); 4.3634 (3.0); 4.3589 (3.6); 4.3412 (3.6); 4.3352 (2.7); 4.3293 (2.0); 4.3231 (2.2); 4.3147 (2.8); 4.3024 (1.4); 4.1709 (0.4); 4.1472 (0.4); 2.7775 (0.9); 2.7564 (0.4); 2.7461 (0.5); 2.7149 (0.9); 2.7036 (0.5); 2.6725 (12.7); 2.0836 (1.6); 1.6030 (16.0); 1.3208 (0.7); 1.2969 (1.3); 1.2730 (0.4); 0.1064 (2.4); 0.0367 (26.3)

TABLE 21 Compounds according to formula (13)

Ex No R⁷ R⁸ Q

LogP 13-01 CH₃ H 3-(trifluoromethyl)phenyl

2.88^([a]) In table 21, ″*″ denotes the point of attachment to the pyridazin-4-yl group.

TABLE 22 13-01: ¹H-NMR(400.2 MHz, d₆-DMSO): δ = 8.3350 (1.3); 7.8120 (0.4); 7.7348 (0.4); 7.7165 (0.8); 7.6962 (3.5); 7.6853 (6.8); 7.6760 (1.8); 7.6415 (1.8); 7.6220 (1.0); 7.5837 (1.2); 7.5640 (0.9); 6.4004 (3.2); 6.0510 (0.4); 6.0374 (0.8); 6.0243 (0.7); 6.0111 (1.0); 6.0078 (0.6); 5.9975 (0.5); 5.9941 (1.1); 5.9809 (0.8); 5.9678 (1.0); 5.9542 (0.5); 5.3533 (0.5); 5.3492 (1.5); 5.3445 (1.6); 5.3404 (0.6); 5.3100 (0.5); 5.3058 (1.3); 5.3012 (1.4); 5.2970 (0.6); 5.1856 (0.6); 5.1823 (1.4); 5.1776 (1.4); 5.1743 (0.7); 5.1593 (0.6); 5.1560 (1.3); 5.1513 (1.3); 5.1481 (0.6); 4.4739 (2.0); 4.4703 (3.5); 4.4668 (2.2); 4.4603 (2.2); 4.4567 (3.5); 4.4531 (2.1); 3.3302 (10.7); 2.6206 (3.5); 2.5747 (16.0); 2.5115 (5.5); 2.5071 (11.6); 2.5026 (16.1); 2.4981 (11.8); 2.4937 (5.8); 0.0089 (0.4); 0.0007 (11.1); −0.0076 (0.4)

TABLE 23 Compounds according to formula (14)

Ex No R⁷ R⁸ Q

LogP 14-01 methyl H 3-(trifluoromethyl)phenyl

1.59^([a]) In table 23, ″*″ denotes the point of attachment to the pyridazin-4-yl group.

TABLE 24 14-01: ¹H-NMR(499.9 MHz, d₆-DMSO): δ = 8.1864 (2.7); 7.9128 (5.7); 7.9095 (3.8); 7.8930 (1.0); 7.8730 (5.1); 7.8246 (2.8); 7.8095 (1.7); 7.7633 (2.3); 7.7480 (1.8); 6.2754 (2.8); 6.2720 (2.2); 6.2626 (2.8); 5.1829 (2.1); 5.1780 (2.1); 4.2128 (0.8); 4.2093 (0.5); 4.2062 (0.4); 4.1986 (0.8); 4.1954 (0.5); 3.9584 (1.6); 3.9542 (1.7); 3.9361 (2.1); 3.9320 (2.2); 3.7960 (2.1); 3.7921 (2.3); 3.7736 (1.7); 3.7697 (1.8); 3.5161 (0.4); 3.4921 (53.5); 3.4569 (0.3); 2.7970 (0.4); 2.7638 (16.0); 2.7608 (11.2); 2.6771 (15.2); 2.6741 (13.4); 2.1696 (1.2); 2.1644 (3.1); 2.1613 (2.0); 1.3705 (0.3); 1.3652 (0.8); 1.3620 (0.7); 1.3581 (0.7); 1.3563 (0.6); 1.3510 (1.6); 1.3478 (1.1); 1.3446 (0.7); 1.3367 (0.8); 1.3336 (0.6)

TABLE 25 Compound according to formula (16)

Ex No R⁷ R⁸ Q LogP 16-01 Cl H 3-(trifluoromethyl)phenyl 2.04^([a])

TABLE 26 16-01: ¹H-NMR(300.2 MHz, CDCl3): δ = 10.5580 (16.0); 7.9322 (15.8); 7.8206 (0.6); 7.7859 (1.8); 7.7263 (2.4); 7.6892 (0.8); 7.6636 (3.5); 7.6416 (11.1); 7.6200 (1.4); 7.5996 (5.4); 7.5701 (2.2); 7.5529 (4.4); 7.5427 (4.8); 7.5360 (3.8); 7.5203 (2.8); 7.4913 (0.4); 7.4602 (1.2); 7.4305 (0.4); 7.4165 (0.6); 7.4013 (0.8); 7.3954 (0.8); 7.3774 (1.1); 7.3040 (22.8); 7.2888 (0.5); 7.2787 (0.3); 6.4615 (0.8); 6.4242 (1.0); 3.7775 (0.6); 3.7541 (0.6); 1.6618 (3.9); 1.5797 (0.3); 1.3863 (0.4); 1.3636 (0.9); 1.3401 (1.2); 1.2976 (7.5); 1.2856 (2.9); 1.2620 (1.5); 0.9215 (1.0); 0.8985 (0.8); 0.8740 (0.5); 0.1126 (4.4); 0.0526 (0.7); 0.0419 (18.2); 0.0310 (0.8)

TABLE 27 Compound according to formula (17)

Ex No R⁷ R⁸ Q LogP 17-01 Cl H 3-(trifluoromethyl)phenyl 2.88^([a])

TABLE 28 17-01: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.5770 (3.1); 8.4318 (16.0); 8.0705 (0.4); 7.9391 (16.0); 7.9021 (2.4); 7.8912 (0.5); 7.8754 (0.7); 7.7791 (0.4); 7.6673 (0.6); 7.6366 (1.1); 7.6109 (4.2); 7.5868 (13.7); 7.5641 (3.1); 7.5324 (7.4); 7.5070 (1.8); 7.4856 (3.2); 7.4783 (5.4); 7.4711 (3.4); 7.4617 (2.6); 7.4557 (3.6); 7.3980 (0.5); 7.3719 (0.5); 7.2982 (33.3); 7.2317 (0.5); 7.2023 (0.4); 7.1131 (0.5); 7.0160 (0.5); 6.1094 (0.5); 5.4728 (0.4); 3.8536 (0.5); 3.8439 (1.4); 3.6757 (1.7); 3.5771 (0.3); 3.5687 (0.5); 3.5030 (1.6); 3.4970 (1.8); 3.4515 (2.1); 3.4123 (3.1); 3.3468 (0.4); 3.3327 (1.0); 3.0167 (2.4); 2.9451 (2.1); 2.8681 (0.4); 2.8019 (2.5); 2.7821 (0.4); 2.7550 (1.3); 2.6951 (0.5); 2.6692 (1.5); 2.4815 (0.3); 2.4560 (0.9); 2.4305 (1.0); 2.4048 (0.4); 2.3068 (1.1); 2.2814 (2.6); 2.2696 (0.6); 2.2564 (2.7); 2.2443 (0.7); 2.2316 (1.0); 2.1491 (6.0); 2.0501 (2.4); 1.9364 (11.8); 1.9237 (1.4); 1.9168 (4.1); 1.4698 (4.0); 1.3681 (0.6); 1.3445 (1.1); 1.3210 (0.8); 1.2929 (1.4); 1.2259 (0.4); 1.2004 (0.5); 1.1633 (3.5); 1.1562 (1.4); 1.1482 (0.9); 1.1384 (7.0); 1.1307 (2.7); 1.1233 (1.5); 1.1133 (3.3); 1.1051 (1.4); 1.0983 (0.8); 0.9168 (0.3); 0.1078 (11.8); 0.0956 (0.5); 0.0481 (1.0); 0.0373 (36.4); 0.0264 (1.6)

TABLE 31 Compounds according to formula (19)

Ex No

L—R⁶ LogP Salt 19-01

(2,4-dimethylphenyl)methyl 1.13^([a]) HCl 19-02

[4-(trifluoromethyl)phenyl]methyl 1.27^([a]) HCl 19-03

[4-(difluoromethoxy)phenyl]methyl 3.40^([a]) HCl 19-04

[4-(trifluoromethoxy)phenyl]methyl 1.38^([a]) HCl 19-05

(2,4-dimethylphenyl)methyl 1.16^([a]) HCl 19-06

(2,4-dimethylphenyl)methyl 1.28^([a]) HCl 19-07

[(2,4-dimethylphenyl)thio]methyl 1.42^([a]) HCl 19-08

[4-(difluoromethyl)phenyl]methyl 0.83^([a]) HCl 19-09

(2-bromo-4-methylphenyl)methyl 1.23^([a]) HCl 19-10

[2-chloro-4-(trifluoromethyl)phenyl]methyl 1.43^([a]) HCl 19-11

(2-chloro-4-methylphenyl)methyl 1.09^([a]) HCl 19-12

(3,4-dichlorophenyl)methyl 1.34^([a]) HCl 19-13

(1-methyl-1H-indol-3-yl)methyl 1.23^([a]) TFA 19-14

(4-nitrophenyl)methyl 0.63^([a]) HCl 19-15

(4-methylsulfanylphenyl)methyl 1.14^([a]) HCl 19-16

(2-chloro-4-methoxyphenyl)methyl 1.09^([a]) HCl 19-17

[2-chloro-4-(difluoromethyl)phenyl]methyl 1.18^([a]) HCl 19-18

[2-chloro-4-(difluoromethoxy)phenyl]methyl 1.30^([a]) HCl 19-19

[2-chloro-4-(trifluoromethoxy)phenyl]methyl 1.55^([a]) HCl 19-20

(3-bromo-5-methylphenyl)methyl 1.51^([a]) HCl 19-21

(2-bromo-4-methylphenyl)methyl 1.27^([a]) HCl 19-22

(2-cyclopropyl-4-methylphenyl)methyl 1.48^([a]) HCl In table 31, ″#″ denotes the point of attachment to the L—R⁶ group.

TABLE 32 19-01: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.6438 (0.5); 7.3661 (0.6); 7.3167 (0.5); 7.2990 (107.3); 7.2639 (0.4); 7.2354 (0.5); 7.1375 (1.2); 7.1101 (1.9); 7.0359 (2.6); 7.0282 (2.3); 7.0171 (1.6); 6.9904 (1.0); 6.9484 (0.8); 4.5372 (0.5); 4.5099 (0.4); 4.2226 (0.4); 4.2061 (0.5); 4.0962 (0.4); 3.8770 (0.7); 3.8498 (0.8); 3.8306 (0.6); 3.8113 (0.5); 3.7436 (16.0); 3.7105 (1.5); 3.6820 (1.5); 3.2699 (0.5); 3.2302 (0.7); 3.1379 (0.5); 3.1032 (0.6); 3.0910 (0.7); 3.0610 (0.4); 2.9134 (0.4); 2.8926 (0.7); 2.8630 (0.4); 2.3783 (9.4); 2.3379 (3.1); 2.3211 (13.5); 2.0640 (0.3); 1.7885 (0.7); 1.7676 (0.8); 1.7013 (2.1); 1.6039 (3.8); 1.3928 (1.2); 1.3716 (2.1); 1.3493 (1.3); 1.3233 (0.6); 1.2923 (1.1); 1.2598 (2.2); 1.2395 (1.4); 0.2335 (0.6); 0.1071 (9.8); 0.0771 (0.4); 0.0551 (0.5); 0.0487 (3.2); 0.0380 (131.2); 0.0275 (5.8); −0.0108 (0.4); −0.0221 (0.5); −0.0306 (0.5); −0.1608 (0.5) 19-02: ¹H-NMR(300.2 MHz, d₆-DMSO): δ = 8.3651 (10.2); 7.7615 (11.8); 7.7346 (15.2); 7.6880 (0.5); 7.6309 (0.3); 7.5701 (14.4); 7.5433 (11.2); 7.4918 (0.4); 3.9314 (3.6); 3.9201 (4.8); 3.8822 (7.9); 3.8626 (3.6); 3.8481 (3.5); 3.8425 (3.2); 3.8288 (2.2); 3.8158 (1.3); 3.7302 (0.5); 3.7034 (4.7); 3.6892 (5.3); 3.6641 (4.6); 3.6508 (3.1); 3.5861 (1.0); 3.3564 (16.0); 3.1792 (2.1); 3.1588 (2.2); 3.1330 (4.3); 3.1133 (4.1); 3.0771 (5.0); 3.0508 (4.8); 3.0312 (2.1); 3.0052 (1.9); 2.5337 (7.6); 2.5279 (14.8); 2.5219 (19.4); 2.5160 (14.2); 2.5102 (7.0); 1.2534 (0.4); 0.0278 (0.8); 0.0173 (15.6); 0.0063 (0.8) 19-03: ¹H-NMR(300.2 MHz, d₆-DMSO): δ = 8.3448 (1.4); 7.5005 (1.1); 7.3804 (2.3); 7.3521 (3.0); 7.2536 (2.4); 7.2001 (3.1); 7.1720 (2.3); 7.1498 (0.3); 7.0067 (1.2); 3.9042 (0.6); 3.8943 (0.8); 3.8644 (0.8); 3.8543 (0.9); 3.7826 (0.6); 3.7708 (0.6); 3.6638 (0.9); 3.6490 (0.8); 3.6240 (0.8); 3.6093 (0.8); 3.5861 (16.0); 3.3614 (2.8); 3.0797 (0.5); 3.0610 (0.4); 3.0340 (0.8); 3.0149 (0.8); 2.9573 (0.8); 2.9295 (0.8); 2.9114 (0.5); 2.8834 (0.4); 2.5279 (2.7); 2.5221 (3.4); 2.5163 (2.6); 0.0177 (1.7) 19-04: ¹H-NMR(300.2 MHz, d₆-DMSO): δ = 8.1127 (3.4); 7.4631 (7.7); 7.4341 (16.0); 7.3819 (11.7); 7.3550 (6.2); 3.9068 (2.5); 3.8956 (3.1); 3.8675 (3.4); 3.8564 (4.2); 3.8119 (0.8); 3.7869 (2.2); 3.7746 (2.4); 3.7522 (1.7); 3.7406 (1.0); 3.7270 (0.4); 3.7142 (0.3); 3.6848 (4.2); 3.6698 (3.4); 3.6453 (3.2); 3.6305 (2.6); 3.5861 (0.6); 3.3562 (3.6); 3.0893 (1.4); 3.0686 (1.5); 3.0431 (3.8); 3.0225 (3.6); 2.9992 (4.1); 2.9730 (3.8); 2.9532 (1.7); 2.9268 (1.5); 2.5338 (5.0); 2.5278 (10.6); 2.5218 (14.5); 2.5157 (10.6); 2.5099 (5.0); 0.0280 (0.4); 0.0172 (11.6); 0.0062 (0.5) 19-05: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.9346 (1.8); 7.2989 (17.2); 7.1470 (2.1); 7.1216 (3.0); 7.0363 (3.7); 7.0169 (2.2); 6.9911 (1.5); 3.9223 (0.9); 3.8910 (1.2); 3.8479 (0.4); 3.8296 (0.8); 3.8103 (1.0); 3.7631 (1.9); 3.7436 (7.7); 3.7263 (1.1); 3.7103 (0.7); 3.7050 (0.7); 3.6845 (0.5); 3.4173 (0.7); 3.3824 (0.9); 3.3726 (0.9); 3.1976 (0.7); 3.1618 (0.8); 3.1544 (0.8); 3.1198 (0.5); 2.3904 (14.8); 2.3184 (16.0); 1.7116 (3.4); 1.4012 (0.4); 1.3776 (0.7); 1.3539 (0.4); 0.0489 (0.8); 0.0380 (21.8); 0.0270 (0.8) 19-06: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.9132 (1.8); 7.2991 (19.2); 7.1628 (0.4); 7.1461 (2.2); 7.1206 (3.1); 7.0718 (1.1); 7.0458 (2.9); 7.0329 (5.5); 7.0083 (2.9); 6.9838 (1.8); 5.2500 (0.5); 5.2354 (0.5); 5.2238 (0.5); 5.2099 (0.5); 3.9307 (1.2); 3.8997 (1.4); 3.8285 (0.6); 3.8111 (1.0); 3.7951 (1.1); 3.7645 (2.4); 3.7470 (1.6); 3.7325 (1.5); 3.7280 (1.4); 3.7099 (2.4); 3.6956 (1.9); 3.6757 (0.4); 3.6486 (1.7); 3.6250 (1.6); 3.6115 (0.9); 3.5881 (0.8); 3.4217 (0.8); 3.3895 (1.1); 3.3756 (1.0); 3.1983 (0.9); 3.1620 (0.9); 3.1508 (1.6); 3.1290 (0.9); 3.1187 (0.7); 3.1045 (1.1); 3.0833 (1.0); 2.9046 (1.1); 2.8779 (1.0); 2.8587 (0.7); 2.8322 (0.7); 2.3885 (15.7); 2.3747 (10.8); 2.3277 (12.3); 2.3178 (16.0); 1.6923 (3.7); 1.6375 (0.4); 1.6139 (0.6); 1.4807 (0.4); 1.4709 (0.4); 1.4213 (0.4); 1.4130 (0.4); 1.2944 (1.2); 0.9418 (0.4); 0.9205 (1.0); 0.8965 (0.4); 0.0488 (0.9); 0.0385 (23.9); 0.0277 (1.0) 19-07: ¹H-NMR(300.2 MHz, d₆-DMSO): δ = 8.6579 (0.8); 7.4235 (0.6); 7.3971 (0.7); 7.1170 (0.7); 7.0699 (0.4); 7.0435 (0.3); 4.0532 (1.1); 4.0402 (1.1); 3.5863 (16.0); 3.3664 (2.3); 3.2852 (0.4); 3.2666 (0.3); 3.1844 (0.4); 3.1563 (0.3); 2.5335 (0.4); 2.5279 (0.7); 2.5219 (0.9); 2.5159 (0.7); 2.3484 (3.4); 2.2743 (3.3); 0.0182 (0.5) 19-08: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.8682 (0.5); 7.5387 (0.6); 7.5121 (1.0); 7.4409 (1.1); 7.4143 (0.7); 7.2988 (1.6); 6.6564 (0.7); 6.4687 (0.3); 3.9633 (0.3); 3.9282 (0.5); 3.7411 (16.0); 0.1055 (0.4); 0.0356 (2.3) 19-09: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.9628 (1.0); 7.4374 (1.8); 7.3198 (1.3); 7.2993 (6.0); 7.2946 (2.1); 7.1333 (1.0); 7.1104 (0.8); 4.0085 (0.4); 3.9705 (0.7); 3.9301 (0.8); 3.9194 (0.6); 3.7796 (0.7); 3.7622 (0.8); 3.7563 (0.5); 3.7548 (0.5); 3.7534 (0.5); 3.7518 (0.5); 3.7427 (16.0); 3.7307 (0.3); 3.7219 (0.5); 3.5169 (0.4); 3.4989 (0.4); 3.4709 (0.6); 3.4532 (0.5); 3.3356 (0.6); 3.3039 (0.6); 3.2899 (0.4); 3.2582 (0.4); 2.3388 (7.4); 1.7299 (1.1); 0.1070 (2.0); 0.0483 (0.3); 0.0375 (8.3) 19-10: ¹H-NMR(300.2 MHz, CDCl3): δ = 9.0001 (0.7); 7.7214 (1.0); 7.6215 (0.3); 7.5948 (1.0); 7.5742 (0.8); 7.2987 (3.6); 4.0018 (0.4); 3.9605 (0.5); 3.9499 (0.4); 3.7420 (16.0); 3.7314 (0.5); 3.7298 (0.5); 3.7285 (0.5); 3.7032 (0.3); 3.5700 (0.4); 3.4327 (0.4); 3.4011 (0.4); 1.7790 (0.4); 0.1060 (0.5); 0.0363 (5.2) 19-11: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.3110 (3.0); 7.2987 (10.0); 7.2853 (3.6); 7.2445 (3.7); 7.0862 (2.0); 7.0833 (2.0); 7.0605 (1.7); 3.9922 (0.7); 3.9792 (1.0); 3.9628 (1.0); 3.9489 (2.1); 3.9398 (1.6); 3.9083 (1.9); 3.8973 (1.3); 3.7592 (1.4); 3.7416 (11.2); 3.7191 (1.2); 3.7016 (0.9); 3.4903 (0.7); 3.4720 (0.8); 3.4444 (1.4); 3.4266 (1.2); 3.3066 (1.2); 3.2747 (1.2); 3.2603 (1.0); 3.2297 (0.8); 2.3404 (16.0); 0.1069 (3.3); 0.0479 (0.6); 0.0372 (13.0); 0.0262 (0.4) 19-12: ¹H-NMR(300.2 MHz, d₆-DMSO): δ = 8.5130 (0.6); 7.6534 (0.8); 7.6379 (0.9); 7.6311 (1.1); 7.6263 (1.1); 7.3496 (0.5); 7.3431 (0.4); 7.3221 (0.4); 7.3155 (0.4); 3.9050 (0.4); 3.7472 (0.4); 3.7322 (0.3); 3.5870 (16.0); 3.3605 (5.8); 3.0564 (0.4); 3.0350 (0.3); 3.0075 (0.4); 2.9826 (0.4); 2.5287 (1.0); 2.5228 (1.4); 2.5169 (1.0); 0.0181 (0.4) 19-14: ¹H-NMR(400.1 MHz, d₆-DMSO): δ = 8.4809 (9.4); 8.2759 (0.4); 8.2398 (14.0); 8.2189 (16.0); 8.1999 (2.1); 8.1799 (0.4); 8.1574 (0.4); 8.0897 (0.9); 7.6671 (0.4); 7.6147 (14.1); 7.5938 (14.2); 7.5753 (1.9); 3.9090 (7.4); 3.8842 (8.2); 3.7360 (0.4); 3.6985 (3.5); 3.6855 (4.6); 3.6661 (4.0); 3.6537 (2.5); 3.6069 (0.5); 3.5675 (2.6); 3.5449 (1.8); 3.4262 (1587.9); 3.2834 (0.9); 3.2378 (0.6); 3.1997 (2.4); 3.1844 (2.5); 3.1651 (4.6); 3.1501 (4.4); 3.1134 (4.6); 3.0943 (4.5); 3.0793 (2.5); 3.0597 (2.2); 3.0314 (1.1); 3.0196 (1.3); 3.0028 (0.8); 2.5083 (24.0) 19-15: ¹H-NMR(400.1 MHz, d₆-DMSO): δ = 8.3662 (3.7); 7.9724 (1.6); 7.2680 (2.1); 7.2613 (1.7); 7.2463 (16.0); 7.2415 (14.2); 7.2250 (10.7); 7.2009 (0.6); 5.3558 (0.3); 3.8614 (1.5); 3.8536 (1.8); 3.8311 (1.9); 3.8235 (2.2); 3.7599 (1.2); 3.7139 (0.5); 3.7010 (0.7); 3.6805 (0.7); 3.6669 (0.6); 3.6512 (0.4); 3.6343 (2.3); 3.6231 (2.1); 3.6040 (2.1); 3.5929 (1.9); 3.5686 (3.9); 3.4925 (6.0); 3.4244 (1340.4); 3.3430 (1.6); 3.3241 (0.8); 3.3053 (0.9); 3.2854 (0.9); 3.0030 (1.2); 2.9884 (1.2); 2.9685 (2.0); 2.9538 (1.9); 2.8951 (2.0); 2.8732 (2.3); 2.8601 (1.6); 2.8385 (2.1); 2.8240 (1.1); 2.7994 (1.2); 2.7776 (1.1); 2.7661 (0.6); 2.7437 (0.5); 2.5084 (16.9); 2.4640 (29.0); 2.4587 (17.0); 2.4306 (0.5); 2.4211 (0.4); 1.3543 (0.5) 19-16: ¹H-NMR(400.1 MHz, d₆-DMSO): δ = 8.4813 (2.3); 7.3558 (2.2); 7.3344 (2.4); 7.0779 (2.6); 7.0715 (2.8); 7.0486 (0.3); 6.9553 (1.6); 6.9489 (1.4); 6.9339 (1.5); 6.9276 (1.3); 3.8732 (0.9); 3.8650 (1.0); 3.8430 (1.2); 3.8349 (1.3); 3.8198 (0.6); 3.8103 (0.3); 3.7882 (1.4); 3.7705 (16.0); 3.7404 (0.8); 3.6795 (1.3); 3.6686 (1.1); 3.6494 (1.0); 3.6384 (0.8); 3.5679 (10.9); 3.5503 (0.4); 3.4269 (400.8); 3.3447 (0.4); 3.0942 (0.4); 3.0790 (0.5); 3.0594 (1.5); 3.0444 (2.7); 3.0234 (1.4); 3.0097 (0.4); 2.9882 (0.4); 2.5123 (3.8); 2.5085 (4.8) 19-17: ¹H-NMR(300.2 MHz, d₆-DMSO): δ = 8.5982 (2.8); 8.1942 (0.8); 7.7276 (4.0); 7.7096 (1.9); 7.6521 (1.7); 7.6256 (4.4); 7.6125 (2.5); 7.5992 (3.4); 7.5748 (2.3); 7.5531 (0.7); 7.2650 (1.6); 7.2572 (0.9); 7.0800 (3.6); 7.0716 (1.8); 6.8952 (1.8); 6.8868 (0.9); 5.4431 (0.7); 3.9516 (1.1); 3.9400 (1.6); 3.9018 (2.8); 3.8796 (1.4); 3.7671 (1.6); 3.7540 (1.8); 3.7281 (1.5); 3.7159 (0.9); 3.5866 (1.1); 3.5320 (0.6); 3.4608 (0.8); 3.4468 (0.9); 3.4238 (1.0); 3.3584 (16.0); 3.2148 (3.5); 3.1905 (2.7); 3.1428 (0.3); 3.0988 (1.6); 3.0763 (1.3); 2.5279 (9.2); 2.5222 (11.5); 2.5166 (8.7); 2.3155 (0.3); 0.0183 (5.6) 19-18: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.9078 (1.1); 7.4704 (1.9); 7.4422 (2.2); 7.2986 (5.6); 7.2480 (2.3); 7.2401 (2.4); 7.0924 (1.2); 7.0846 (1.1); 7.0645 (1.1); 7.0568 (1.0); 6.7833 (1.4); 6.5401 (3.0); 6.2969 (1.5); 4.0135 (0.6); 3.9952 (1.5); 3.9581 (1.1); 3.9480 (0.8); 3.7594 (0.8); 3.7550 (0.7); 3.7534 (0.7); 3.7414 (16.0); 3.7308 (0.4); 3.7293 (0.4); 3.7278 (0.4); 3.7191 (0.8); 3.7028 (0.5); 3.5210 (0.5); 3.5032 (0.5); 3.4748 (0.8); 3.4570 (0.7); 3.3437 (0.7); 3.3123 (0.7); 3.2977 (0.6); 3.2661 (0.4); 1.8785 (0.7); 0.1055 (0.8); 0.0356 (7.0) 19-19: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.5131 (0.5); 7.4848 (0.6); 7.3376 (0.6); 7.3329 (0.6); 7.2989 (2.1); 4.0040 (0.4); 3.7415 (16.0); 1.8525 (0.3); 0.0355 (2.6) 19-20: ¹H-NMR(300.2 MHz, d₆-DMSO): δ = 8.5216 (6.7); 7.3467 (11.2); 7.3411 (9.7); 7.1413 (8.8); 3.9265 (2.8); 3.9155 (3.6); 3.8868 (3.4); 3.8762 (5.2); 3.8237 (2.1); 3.7030 (4.5); 3.6880 (4.0); 3.6634 (3.6); 3.6487 (2.8); 3.5874 (0.6); 3.4075 (16.0); 3.0693 (2.0); 3.0494 (2.0); 3.0233 (3.6); 3.0036 (3.4); 2.9316 (3.9); 2.9044 (3.8); 2.8854 (2.3); 2.8585 (2.0); 2.5349 (4.7); 2.5290 (9.6); 2.5230 (12.9); 2.5169 (9.3); 2.5110 (4.4); 2.3826 (0.3); 2.3165 (40.5); 0.0298 (0.4); 0.0190 (8.5); 0.0080 (0.3) 19-21: ¹H-NMR(300.2 MHz, d₆-DMSO): δ = 8.6186 (1.2); 7.5130 (1.6); 7.5105 (1.6); 7.3597 (1.2); 7.3338 (1.7); 7.2347 (1.0); 7.2315 (0.9); 7.2088 (0.7); 7.2057 (0.6); 3.9187 (0.5); 3.9074 (0.6); 3.8792 (0.6); 3.8681 (0.9); 3.8089 (0.4); 3.7192 (0.8); 3.7047 (0.7); 3.6797 (0.6); 3.6655 (0.5); 3.5866 (2.4); 3.3809 (16.0); 3.1318 (0.9); 3.1154 (1.3); 3.0882 (0.8); 2.5350 (0.8); 2.5290 (1.6); 2.5230 (2.1); 2.5169 (1.5); 2.5110 (0.7); 2.3116 (6.9); 0.0179 (1.5) 19-22: ¹H-NMR(300.2 MHz, d₆-DMSO): δ = 8.5284 (3.2); 7.1867 (2.2); 7.1255 (2.7); 7.1000 (3.9); 6.9895 (2.2); 6.9639 (1.6); 6.8054 (3.6); 3.8936 (1.1); 3.8837 (1.4); 3.8539 (1.4); 3.8442 (1.9); 3.8256 (0.5); 3.8117 (0.8); 3.7951 (1.1); 3.7813 (1.0); 3.7683 (0.8); 3.6825 (1.8); 3.6685 (1.5); 3.6427 (1.4); 3.6291 (1.1); 3.3544 (8.5); 3.2607 (0.8); 3.2444 (0.8); 3.2148 (1.4); 3.1981 (1.2); 3.0841 (1.4); 3.0522 (1.4); 3.0382 (1.0); 3.0063 (1.0); 2.5340 (3.1); 2.5281 (6.2); 2.5221 (8.2); 2.5161 (6.0); 2.5103 (2.8); 2.3061 (1.4); 2.2555 (16.0); 2.0957 (0.3); 2.0784 (0.8); 2.0685 (0.9); 2.0611 (0.7); 2.0506 (1.5); 2.0412 (0.8); 2.0329 (0.9); 2.0230 (0.8); 2.0051 (0.4); 0.9907 (0.7); 0.9754 (2.8); 0.9690 (3.2); 0.9591 (1.6); 0.9550 (1.5); 0.9475 (2.8); 0.9412 (3.1); 0.9276 (0.9); 0.6964 (1.0); 0.6829 (3.0); 0.6768 (3.4); 0.6655 (3.4); 0.6600 (2.8); 0.6463 (0.9); 0.0188 (6.3)

TABLE 29 Compounds according to formula (20)

Ex No R⁷ R⁸ Q

L—R6 LogP 20- 01 Cl H 3-(trifluoro- methyl)phenyl

(2,4-dimethyl- phenyl)methyl 4.34^([a]) 20- 02 Cl H 3-(trifluoro- methyl)phenyl

(2,4-dimethyl- phenyl)methyl 4.49^([a]) 20- 03 Cl H 3-(trifluoro- methyl)phenyl

(4-chlorophenyl)methyl 4.15^([a]) 20- 04 CH₃ H 3-cyclopropyl- 2-fluorophenyl

(2,4-dimethyl- phenyl)methyl 3.94^([a]) 20- 05 Cl H 3-(trifluoro- methyl)phenyl

[4-(trifluoro- methyl)phenyl]methyl 4.32^([a]) 20- 06 Cl H 3-(trifluoro- methyl)phenyl

[4-(difluoro- methoxy)phenyl]methyl 3.91^([a]) 20- 07 Cl H 3-(trifluoro- methyl)phenyl

[4-(trifluoro- methoxy)phenyl]methyl 4.37^([a]) 20- 08 Cl H 3-(trifluoro- methyl)phenyl

(2,4- dimethylphenyl)methyl 2.77^([a]) 20- 09 CH₃ H 3-cyclopropyl- 2-fluorophenyl

(2,4- dimethylphenyl)methyl 3.98^([a]) 20- 10 CH₃ H 3-cyclopropyl- 2-fluorophenyl

(2-bromo-4-methyl- phenyl)methyl 4.12^([a]) 20- 11 CH₃ H 3-cyclopropyl- 2-fluorophenyl

(3,4-dichloro- phenyl)methyl 4.15^([a]) 20- 12 Cl H 3-(trifluoro- methyl)phenyl

[4-(difluoro- methyl)phenyl]methyl 3.87^([a]) 20- 13 CH₃ H 3-cyclopropyl- 2-fluorophenyl

[2-chloro-4-(trifluoro- methyl)phenyl]methyl 4.30^([a]) 20- 14 CH₃ H 3-cyclopropyl- 2-fluorophenyl

(2-chloro-4-methyl- phenyl)methyl 4.05^([a]) 20- 15 Cl H 3-(trifluoro- methyl)phenyl

(4-nitrophenyl)methyl 3.71^([a]) 20- 16 Cl H 3-(trifluoro- methyl)phenyl

[4-(trifluoromethyl- thio)phenyl]methyl 4.67^([a]) 20- 17 CH₃ H 3-chloro-2- fluorophenyl

(2-chloro-4-methyl- phenyl)methyl 3.88^([a]) 20- 18 CH₃ H 3-cyclopropyl- 2-fluorophenyl

(2-chloro-4-methoxy- phenyl)methyl 3.81^([a]) 20- 19 CH₃ H 3-(difluoro- methyl)phenyl

(2-chloro-4-methyl- phenyl)methyl 3.49^([a]) 20- 20 CH₃ H 3-cyclopropyl- 2-fluorophenyl

[2-chloro-4-(difluoro- methyl)phenyl]methyl 3.86^([a]) 20- 21 CH₃ H 3-cyclopropyl- 2-fluorophenyl

[2-chloro-4-(difluoro- methoxy)phenyl]methyl 4.02^([a]) 20- 22 CH₃ H 3-cyclopropyl- 2-fluorophenyl

[2-chloro-4-(trifluoro- methoxy)phenyl]methyl 4.51^([a]) 20- 23 CH₃ H 3-cyclopropyl- 2-fluorophenyl

(2-bromo-4-methyl- phenyl)methyl 4.12^([a]) 20- 24 CH₃ H 3-cyclopropyl- 2-fluorophenyl

(3-bromo-5-methyl- phenyl)methyl 4.32^([a]) 20- 25 Cl H 3-cyclopropyl- phenyl

(2,4- dimethylphenyl)methyl 4.51^([a]) 20- 26 Cl H 3-cyclopropyl- 2-fluorophenyl

(2,4- dimethylphenyl)methyl 4.62^([a]) 20- 27 Cl H 3-(difluoro- methyl)phenyl

(2,4- dimethylphenyl)methyl 4.05^([a]) 20- 28 Cl H 3-bromophenyl

(2,4- dimethylphenyl)methyl 4.40^([a]) 20- 29 Cl H 3-chlorophenyl

(2,4- dimethylphenyl)methyl 4.33^([a]) 20- 30 CH₃ H 2-fluoro-3- (trifluoro- methyl)phenyl

(2,4- dimethylphenyl)methyl 4.01^([a]) 20- 31 Cl H 3-(difluoro- methyl)phenyl

(2-bromo-4-methyl- phenyl)methyl 4.15^([a]) 20- 32 Cl H 3-cyclopropyl- 2-fluorophenyl

(4-bromo-2-methyl- phenyl)methyl 4.74^([a]) 20- 33 CH₃ H 3-cyclopropyl- 2-fluorophenyl

(4-bromo-2-methyl- phenyl)methyl 4.19_([a]) 20- 34 Cl H 3-cyclopropyl- phenyl

(2-bromo-4-methyl- phenyl)methyl 4.62^([a]) 20- 35 Cl H 3-cyclopropyl- 2-fluorophenyl

(2-bromo-4-methyl- phenyl)methyl 4.74^([a]) 20- 36 CH₃ H 3-cyclopropyl- 2-fluorophenyl

(2-cyclopropyl-4- methylphenyl)methyl 4.24^([a]) In table 29, ″#″ denotes the point of attachment to the L—R⁶ group and ″*″ denotes the point of attachment to the pyridazin-4-yl group.

TABLE 30 20-01: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.6137 (0.6); 7.5864 (2.6); 7.5738 (2.3); 7.5673 (5.6); 7.5651 (5.6); 7.5531 (0.7); 7.5184 (0.3); 7.4835 (0.5); 7.4473 (2.9); 7.4262 (0.4); 7.4022 (0.5); 7.3866 (1.1); 7.3761 (1.5); 7.3690 (1.4); 7.3563 (1.2); 7.3485 (0.8); 7.2992 (8.7); 7.0071 (1.7); 6.9893 (4.8); 6.9670 (0.5); 6.9438 (3.7); 6.9272 (0.6); 6.9165 (1.7); 6.2302 (3.6); 5.6560 (1.5); 5.6183 (1.5); 5.3382 (1.4); 3.8359 (0.5); 3.8223 (0.6); 3.7993 (2.5); 3.7851 (4.4); 3.7660 (2.5); 3.7479 (0.6); 3.7296 (0.7); 3.4491 (0.7); 3.4331 (0.7); 3.4164 (0.5); 3.3963 (0.3); 3.0941 (1.1); 3.0840 (1.1); 3.0481 (1.5); 3.0378 (1.4); 2.9975 (0.4); 2.9271 (0.4); 2.7997 (1.4); 2.7655 (1.3); 2.7537 (1.2); 2.7194 (1.0); 2.4069 (15.5); 2.3735 (0.4); 2.3469 (1.4); 2.3261 (0.4); 2.2946 (0.4); 2.1032 (1.2); 2.0749 (16.0); 1.6890 (0.4); 1.2937 (0.9); 0.1096 (0.7); 0.0393 (8.8); 0.0286 (0.4) 20-03: ¹H-NMR(499.9 MHz, d₆-DMSO): δ = 10.9854 (5.4); 9.5820 (0.5); 8.1369 (0.4); 7.7406 (0.4); 7.7193 (0.5); 7.7035 (0.5); 7.6942 (0.5); 7.6775 (0.4); 7.6611 (0.4); 7.6379 (0.8); 7.6224 (1.7); 7.6065 (3.2); 7.5932 (0.5); 7.5902 (0.6); 7.4155 (0.3); 7.3802 (3.2); 7.3765 (1.6); 7.3633 (5.8); 7.3424 (0.6); 7.3169 (4.3); 7.3000 (2.6); 7.2776 (0.3); 7.2687 (0.4); 7.2648 (0.4); 7.2518 (0.4); 7.2475 (0.4); 7.2395 (0.6); 7.2305 (0.4); 7.2227 (0.6); 7.2175 (0.5); 7.2051 (0.6); 7.1891 (0.5); 7.1743 (1.0); 7.1707 (1.5); 7.1668 (1.1); 7.1560 (1.3); 7.1521 (1.2); 7.1350 (0.5); 7.1024 (2.0); 7.0643 (0.5); 7.0592 (0.4); 7.0444 (2.9); 7.0271 (3.1); 6.9195 (0.3); 6.9021 (0.4); 6.7815 (3.9); 6.7641 (3.5); 6.7542 (0.5); 5.7593 (0.9); 4.9835 (1.0); 4.9737 (1.9); 4.9637 (0.9); 4.4109 (1.0); 4.3790 (1.2); 4.2791 (0.4); 4.2650 (0.7); 4.2509 (0.4); 4.1803 (1.4); 4.1484 (1.1); 4.1040 (0.5); 4.0926 (0.7); 4.0802 (0.5); 3.7895 (0.4); 3.7594 (0.5); 3.7493 (1.0); 3.7413 (0.8); 3.7301 (1.4); 3.7191 (1.9); 3.7147 (1.0); 3.7071 (1.0); 3.7040 (0.9); 3.7009 (0.9); 3.6946 (1.3); 3.6777 (0.8); 3.6691 (0.9); 3.6588 (16.0); 3.6286 (1.0); 3.5016 (0.6); 3.4918 (1.0); 3.4815 (0.8); 3.4696 (0.8); 3.4599 (0.5); 3.3220 (43.6); 3.1838 (0.6); 3.1709 (0.7); 3.1569 (0.8); 3.1441 (0.7); 2.9661 (0.8); 2.9497 (0.9); 2.9392 (0.7); 2.9229 (0.6); 2.5141 (3.2); 2.5105 (6.2); 2.5069 (8.2); 2.5033 (5.8); 2.4997 (2.7); 2.4288 (0.6); 2.4122 (0.4); 1.2961 (0.5); 1.2826 (1.0); 1.2710 (1.1); 1.2676 (1.2); 1.2502 (2.9); 0.8769 (1.9); 0.8633 (5.2); 0.8490 (2.2) 20-04: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.2990 (28.0); 7.0996 (0.5); 7.0732 (1.3); 7.0455 (1.3); 7.0293 (1.0); 7.0225 (1.1); 7.0000 (1.2); 6.9804 (5.0); 6.9776 (5.5); 6.9156 (1.9); 6.8123 (0.6); 6.8062 (0.6); 6.7886 (1.0); 6.7646 (0.5); 6.7586 (0.4); 6.1773 (1.4); 5.8058 (0.8); 5.7684 (0.8); 4.6349 (0.4); 4.5797 (0.5); 4.1723 (0.4); 4.1484 (0.4); 3.9148 (0.3); 3.8991 (0.4); 3.8775 (1.0); 3.8625 (1.2); 3.8413 (1.1); 3.8314 (1.3); 3.8048 (0.4); 3.7956 (0.4); 3.6822 (0.5); 3.6709 (0.4); 3.6615 (0.4); 2.9929 (0.4); 2.9805 (0.5); 2.9467 (1.0); 2.9342 (0.9); 2.8823 (1.0); 2.8491 (0.9); 2.8360 (0.5); 2.8028 (0.4); 2.5246 (0.7); 2.4914 (11.8); 2.3842 (9.2); 2.3623 (0.7); 2.3501 (0.4); 2.1329 (0.5); 2.1218 (0.6); 2.1055 (0.9); 2.0847 (2.2); 2.0468 (3.1); 2.0279 (5.3); 2.0149 (9.4); 1.8953 (16.0); 1.3213 (0.4); 1.2975 (0.9); 1.2736 (0.4); 1.0638 (0.6); 1.0484 (1.5); 1.0416 (1.6); 1.0270 (1.0); 1.0197 (1.6); 1.0132 (1.6); 0.9988 (0.8); 0.8072 (0.7); 0.7921 (1.8); 0.7864 (1.8); 0.7755 (1.6); 0.7695 (1.9); 0.7536 (0.6); 0.0482 (0.7); 0.0372 (35.8); 0.0263 (1.8) 20-06: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.5997 (1.6); 7.5885 (1.6); 7.5809 (3.7); 7.5659 (0.7); 7.5125 (0.4); 7.4571 (1.8); 7.4101 (0.4); 7.3961 (0.8); 7.3848 (1.1); 7.3775 (1.0); 7.3655 (1.0); 7.3574 (0.6); 7.2984 (16.1); 7.1490 (0.8); 7.1183 (9.4); 7.0957 (0.5); 7.0846 (0.6); 7.0679 (0.6); 6.9863 (0.4); 6.9476 (0.3); 6.8246 (1.2); 6.7247 (1.8); 6.5794 (2.4); 6.3344 (1.2); 5.6259 (1.0); 5.5886 (1.1); 5.3379 (0.6); 4.1953 (1.2); 4.1715 (3.5); 4.1477 (3.6); 4.1240 (1.3); 3.7442 (0.8); 3.7368 (0.4); 3.7140 (1.8); 3.7071 (2.0); 3.6998 (2.0); 3.6899 (1.9); 3.4969 (0.3); 3.4814 (0.4); 3.4660 (0.5); 3.4438 (0.5); 3.4295 (0.4); 3.4130 (0.3); 3.0725 (0.7); 3.0579 (0.7); 3.0268 (1.2); 3.0124 (1.1); 2.8982 (1.1); 2.8687 (1.0); 2.8525 (0.7); 2.8229 (0.6); 2.0845 (16.0); 1.6278 (0.8); 1.3208 (4.3); 1.2970 (8.5); 1.2732 (4.0); 0.1062 (4.5); 0.0472 (0.6); 0.0363 (17.7); 0.0256 (0.7) 20-07: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.6445 (0.5); 7.6275 (1.0); 7.6012 (7.0); 7.5960 (6.2); 7.5911 (6.1); 7.5834 (15.9); 7.5802 (16.0); 7.5657 (1.7); 7.5159 (0.8); 7.4607 (7.4); 7.4305 (0.4); 7.4137 (1.2); 7.3989 (3.2); 7.3869 (4.6); 7.3801 (4.2); 7.3690 (3.4); 7.3608 (2.3); 7.3210 (0.8); 7.2984 (52.3); 7.2151 (7.2); 7.1918 (17.9); 7.1763 (25.5); 7.1550 (3.0); 7.1466 (5.3); 6.9474 (0.3); 6.7551 (8.7); 5.6253 (4.5); 5.5877 (4.8); 4.1967 (0.8); 4.1729 (2.4); 4.1491 (2.5); 4.1253 (0.9); 3.7456 (0.9); 3.7311 (1.4); 3.7085 (7.9); 3.7012 (8.9); 3.6941 (8.9); 3.6841 (8.8); 3.6643 (1.1); 3.6471 (1.5); 3.6277 (0.4); 3.6172 (0.3); 3.5319 (0.6); 3.5165 (1.3); 3.5014 (1.8); 3.4862 (2.1); 3.4794 (1.8); 3.4709 (2.0); 3.4654 (1.9); 3.4494 (1.8); 3.4338 (1.3); 3.4194 (0.5); 3.0973 (3.1); 3.0821 (3.1); 3.0515 (5.0); 3.0364 (4.6); 2.9236 (4.7); 2.8944 (4.3); 2.8777 (3.1); 2.8487 (2.7); 2.0852 (11.4); 1.6150 (4.0); 1.3218 (3.4); 1.2980 (6.7); 1.2741 (3.0); 0.9180 (0.4); 0.1196 (0.4); 0.1075 (12.3); 0.0954 (0.6); 0.0485 (2.4); 0.0377 (70.0); 0.0267 (2.7) 20-09: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.2986 (10.3); 7.1030 (0.6); 7.0759 (1.7); 7.0486 (1.8); 7.0364 (1.2); 7.0295 (1.4); 7.0127 (1.2); 7.0071 (1.4); 6.9858 (0.9); 6.9700 (6.6); 6.9464 (0.4); 6.9130 (2.5); 6.8158 (0.8); 6.8092 (0.8); 6.7922 (1.2); 6.7675 (0.7); 6.7621 (0.6); 6.1817 (2.0); 5.7998 (1.1); 5.7626 (1.2); 5.3377 (2.4); 3.9131 (0.5); 3.8984 (0.6); 3.8768 (1.4); 3.8620 (1.6); 3.8395 (1.4); 3.8298 (1.6); 3.8030 (0.6); 3.7933 (0.6); 3.7218 (0.3); 3.6876 (0.6); 3.6755 (0.6); 3.6659 (0.4); 3.6542 (0.4); 2.9858 (0.6); 2.9736 (0.6); 2.9399 (1.3); 2.9278 (1.2); 2.8756 (1.2); 2.8427 (1.1); 2.8298 (0.7); 2.7968 (0.6); 2.4971 (16.0); 2.3837 (11.9); 2.1362 (0.5); 2.1247 (0.6); 2.1079 (1.0); 2.0853 (1.4); 2.0801 (0.7); 2.0622 (0.4); 2.0083 (11.8); 1.3221 (0.5); 1.2983 (1.1); 1.2745 (0.4); 1.0656 (0.8); 1.0504 (1.9); 1.0436 (2.2); 1.0376 (1.2); 1.0290 (1.2); 1.0218 (2.1); 1.0151 (2.0); 1.0008 (1.0); 0.9204 (0.7); 0.8097 (1.0); 0.7949 (2.4); 0.7924 (2.2); 0.7887 (2.4); 0.7778 (2.2); 0.7722 (2.5); 0.7559 (0.8); 0.1081 (2.5); 0.0492 (0.6); 0.0384 (13.8); 0.0275 (0.6) 20-10: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.2990 (19.4); 7.1801 (1.1); 7.1543 (3.8); 7.1373 (2.2); 7.1106 (0.7); 7.0974 (0.6); 7.0707 (1.7); 7.0437 (2.0); 7.0364 (1.3); 7.0290 (1.4); 7.0129 (1.2); 7.0074 (1.3); 6.9862 (0.6); 6.9804 (0.5); 6.8524 (0.4); 6.8092 (0.9); 6.8021 (0.9); 6.7860 (1.4); 6.7611 (0.7); 6.7552 (0.6); 6.3131 (2.6); 5.8564 (1.0); 5.8193 (1.0); 5.3386 (7.0); 3.9895 (0.3); 3.9667 (0.9); 3.9567 (1.6); 3.9401 (0.8); 3.9283 (1.8); 3.9166 (1.2); 3.8196 (1.4); 3.7922 (1.0); 3.1019 (0.6); 3.0886 (0.6); 3.0567 (1.3); 3.0435 (1.2); 2.9815 (1.0); 2.9497 (1.0); 2.9364 (0.6); 2.9042 (0.5); 2.5377 (16.0); 2.3979 (11.7); 2.1410 (0.5); 2.1298 (0.6); 2.1132 (1.0); 2.0959 (0.6); 2.0848 (0.6); 1.6159 (1.2); 1.2923 (0.4); 1.0623 (0.7); 1.0470 (2.0); 1.0403 (2.2); 1.0257 (1.2); 1.0185 (2.1); 1.0119 (2.0); 0.9975 (0.9); 0.8060 (1.0); 0.7912 (2.4); 0.7852 (2.3); 0.7742 (2.2); 0.7688 (2.4); 0.7524 (0.7); 0.1073 (6.5); 0.0487 (1.1); 0.0379 (24.0); 0.0271 (1.2) 20-11: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.6035 (0.6); 7.4458 (0.7); 7.4278 (2.0); 7.4208 (3.0); 7.4034 (2.4); 7.3940 (1.0); 7.3789 (3.9); 7.3518 (3.7); 7.2985 (19.8); 7.2200 (2.9); 7.2134 (3.0); 7.1980 (0.5); 7.1689 (0.4); 7.1470 (0.6); 7.1223 (0.9); 7.1149 (1.0); 7.0872 (2.0); 7.0593 (1.7); 7.0348 (1.2); 7.0284 (1.5); 7.0053 (1.8); 6.9919 (1.8); 6.9850 (2.2); 6.9646 (1.5); 6.9578 (1.4); 6.9211 (1.2); 6.8482 (0.4); 6.8340 (0.9); 6.8277 (1.0); 6.8092 (1.4); 6.7858 (0.8); 6.7807 (0.7); 6.6546 (1.5); 5.7742 (0.7); 5.7382 (0.8); 4.6344 (6.3); 3.8233 (0.4); 3.8083 (0.6); 3.7869 (1.1); 3.7710 (1.4); 3.7459 (1.4); 3.7363 (1.9); 3.7073 (1.4); 3.6780 (1.0); 3.6679 (0.7); 3.6548 (0.6); 2.9519 (0.6); 2.9215 (3.6); 2.8996 (2.6); 2.7552 (0.6); 2.5983 (16.0); 2.3497 (0.4); 2.2796 (0.4); 2.1375 (0.7); 2.1268 (0.8); 2.1097 (1.2); 2.0919 (0.8); 2.0815 (0.8); 2.0644 (0.4); 1.7108 (0.8); 1.2937 (0.6); 1.0723 (1.1); 1.0568 (2.4); 1.0500 (2.6); 1.0356 (1.5); 1.0284 (2.4); 1.0219 (2.3); 1.0074 (1.0); 0.8293 (0.4); 0.8158 (1.5); 0.8006 (2.9); 0.7959 (3.0); 0.7842 (2.4); 0.7786 (2.9); 0.7619 (1.0); 0.1073 (2.7); 0.0484 (0.6); 0.0376 (21.7); 0.0268 (1.0) 20-12: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.3093 (0.9); 7.6816 (0.5); 7.6643 (0.5); 7.5937 (0.8); 7.5847 (0.7); 7.5761 (1.6); 7.5734 (1.6); 7.5379 (0.4); 7.5109 (1.1); 7.4844 (1.4); 7.4514 (1.2); 7.4285 (1.0); 7.4012 (0.7); 7.3938 (0.9); 7.3856 (0.7); 7.3735 (0.9); 7.3669 (0.8); 7.3560 (0.5); 7.3474 (0.4); 7.2987 (4.0); 7.2418 (1.3); 7.2155 (1.0); 6.8947 (0.4); 6.7069 (0.9); 6.6275 (0.4); 6.5592 (0.7); 6.5192 (0.4); 5.6695 (0.4); 5.6321 (0.4); 4.6345 (1.1); 3.7463 (16.0); 3.7371 (0.6); 3.7326 (0.9); 3.7213 (1.1); 3.7045 (1.0); 3.6929 (0.3); 3.1207 (0.5); 3.0897 (0.5); 3.0759 (0.5); 2.9477 (0.4); 2.9172 (0.4); 2.0862 (0.6); 0.1077 (0.6); 0.0372 (5.6) 20-13: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.5433 (2.7); 7.5349 (1.4); 7.5067 (1.7); 7.4396 (2.2); 7.4132 (1.3); 7.2988 (15.3); 7.1016 (0.7); 7.0780 (1.8); 7.0492 (1.6); 7.0211 (1.1); 7.0150 (1.3); 6.9971 (1.2); 6.9920 (1.4); 6.9706 (0.7); 6.9650 (0.6); 6.8218 (0.8); 6.8162 (0.8); 6.7956 (1.3); 6.7737 (0.7); 6.7685 (0.6); 6.4365 (2.0); 5.8781 (1.1); 5.8413 (1.1); 5.3378 (4.7); 4.0144 (0.3); 3.9961 (0.5); 3.9821 (0.6); 3.9505 (1.2); 3.9138 (1.5); 3.9005 (1.1); 3.8136 (1.2); 3.8050 (1.4); 3.7773 (0.9); 3.7682 (0.7); 3.2292 (0.6); 3.2147 (0.6); 3.1842 (1.2); 3.1698 (1.1); 3.0953 (1.1); 3.0642 (1.0); 3.0504 (0.7); 3.0194 (0.6); 2.5406 (16.0); 2.1338 (0.5); 2.1238 (0.6); 2.1058 (1.0); 2.0845 (0.8); 2.0775 (0.6); 1.6213 (1.5); 1.3047 (0.6); 1.2977 (0.7); 1.0686 (0.7); 1.0534 (1.9); 1.0466 (2.2); 1.0320 (1.2); 1.0248 (2.1); 1.0182 (2.0); 1.0038 (1.0); 0.9199 (0.4); 0.8094 (0.9); 0.7945 (2.3); 0.7919 (2.2); 0.7885 (2.3); 0.7775 (2.2); 0.7719 (2.5); 0.7557 (0.8); 0.1075 (1.9); 0.0488 (0.7); 0.0379 (21.3); 0.0270 (1.0) 20-14: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.2990 (16.3); 7.1616 (1.7); 7.1361 (3.0); 7.0973 (3.2); 7.0816 (2.0); 7.0698 (2.0); 7.0555 (1.2); 7.0426 (2.0); 7.0336 (1.2); 7.0265 (1.4); 7.0101 (1.2); 7.0046 (1.4); 6.9834 (0.6); 6.9775 (0.6); 6.8100 (0.8); 6.8029 (0.8); 6.7865 (1.3); 6.7621 (0.7); 6.7564 (0.6); 6.3830 (2.4); 5.8550 (0.9); 5.8179 (0.9); 4.1959 (0.4); 4.1722 (1.1); 4.1484 (1.1); 4.1248 (0.4); 3.9303 (1.2); 3.8988 (1.8); 3.8600 (0.4); 3.7998 (1.4); 3.7727 (1.0); 3.1118 (0.6); 3.0983 (0.6); 3.0662 (1.0); 3.0527 (0.9); 2.9676 (1.0); 2.9376 (0.9); 2.9229 (0.6); 2.8918 (0.5); 2.5405 (16.0); 2.3929 (11.4); 2.3381 (0.4); 2.1375 (0.5); 2.1265 (0.6); 2.1089 (1.0); 2.0841 (5.8); 2.0634 (0.4); 1.6411 (1.0); 1.3213 (1.5); 1.2975 (2.9); 1.2737 (1.3); 1.0598 (0.7); 1.0445 (1.9); 1.0377 (2.0); 1.0232 (1.2); 1.0159 (2.0); 1.0092 (1.9); 0.9951 (1.0); 0.9732 (0.4); 0.8042 (0.9); 0.7892 (2.2); 0.7833 (2.2); 0.7723 (2.1); 0.7665 (2.5); 0.7503 (0.8); 0.1071 (4.8); 0.0486 (0.6); 0.0376 (20.4); 0.0266 (0.9) 20-15: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.3004 (1.5); 8.2075 (15.1); 8.1785 (16.0); 8.1419 (0.4); 7.6878 (0.7); 7.6706 (1.0); 7.6446 (0.6); 7.6223 (0.9); 7.5945 (10.8); 7.5771 (15.7); 7.5518 (1.2); 7.5391 (1.4); 7.5241 (0.7); 7.5026 (1.5); 7.4794 (1.8); 7.4290 (10.0); 7.4020 (4.0); 7.3834 (3.1); 7.3699 (4.5); 7.3558 (7.6); 7.3469 (17.9); 7.3327 (3.8); 7.3179 (14.8); 7.2989 (56.2); 7.2734 (0.8); 7.2312 (0.7); 7.1957 (0.5); 7.1205 (0.3); 6.8042 (8.5); 5.6595 (4.5); 5.6224 (4.8); 5.3382 (11.5); 4.6350 (9.2); 4.1727 (0.8); 4.1488 (1.1); 4.1257 (0.8); 4.1040 (1.0); 4.0815 (0.5); 3.8156 (0.3); 3.7756 (0.4); 3.7524 (1.0); 3.7375 (1.3); 3.7150 (8.0); 3.7087 (8.6); 3.7004 (9.3); 3.6916 (9.2); 3.6544 (1.5); 3.6212 (0.8); 3.6068 (1.5); 3.5923 (2.0); 3.5772 (2.3); 3.5635 (2.1); 3.5558 (2.0); 3.5404 (1.8); 3.5250 (1.4); 3.2529 (0.4); 3.2292 (0.4); 3.2232 (0.5); 3.2033 (2.8); 3.1883 (2.8); 3.1577 (4.9); 3.1434 (4.6); 3.1189 (0.4); 3.0493 (4.6); 3.0201 (4.2); 3.0044 (2.9); 2.9751 (2.5); 2.3936 (1.1); 2.0855 (7.2); 2.0729 (0.5); 2.0461 (0.4); 1.9397 (1.4); 1.7942 (0.4); 1.7851 (0.5); 1.6711 (2.1); 1.6480 (2.5); 1.6234 (2.3); 1.5582 (1.1); 1.5049 (0.5); 1.4837 (0.5); 1.4559 (0.5); 1.4337 (0.6); 1.4067 (0.6); 1.3810 (0.5); 1.3449 (0.6); 1.3217 (1.7); 1.2978 (3.0); 1.2834 (1.3); 1.2741 (1.3); 1.2600 (0.5); 1.0113 (0.4); 0.9982 (1.0); 0.9731 (1.7); 0.9587 (0.3); 0.9482 (0.7); 0.9175 (0.4); 0.1192 (0.8); 0.1072 (22.3); 0.0481 (2.1); 0.0373 (71.4); 0.0281 (2.8); 0.0264 (3.2); −0.0286 (0.4) 20-16: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.3054 (3.9); 8.0981 (0.6); 8.0728 (0.6); 7.6857 (2.4); 7.6685 (3.0); 7.6494 (11.3); 7.6227 (13.0); 7.6036 (8.0); 7.5940 (6.5); 7.5832 (16.0); 7.5556 (1.8); 7.5073 (1.0); 7.4944 (0.6); 7.4579 (8.1); 7.4222 (2.7); 7.4036 (2.9); 7.3961 (3.5); 7.3840 (5.3); 7.3770 (5.6); 7.3721 (5.4); 7.3452 (2.9); 7.2987 (52.2); 7.2196 (14.2); 7.1925 (12.5); 7.1496 (0.9); 7.1242 (2.0); 7.0409 (0.5); 7.0189 (0.4); 6.9480 (0.5); 6.7538 (0.6); 6.7061 (7.6); 5.6396 (4.2); 5.6023 (4.3); 4.7827 (0.4); 4.7719 (0.5); 4.7602 (0.4); 4.6354 (4.6); 4.1042 (0.4); 4.0277 (0.7); 3.9809 (1.0); 3.8507 (0.6); 3.8367 (0.6); 3.8118 (0.9); 3.7985 (1.0); 3.7579 (0.9); 3.7442 (1.2); 3.7213 (6.8); 3.7123 (8.5); 3.7077 (8.6); 3.6953 (8.2); 3.6760 (1.1); 3.6577 (1.7); 3.6283 (0.4); 3.5633 (0.6); 3.5462 (1.2); 3.5320 (1.7); 3.5169 (2.0); 3.5017 (1.8); 3.4791 (1.6); 3.4635 (1.1); 3.4482 (0.4); 3.2155 (0.4); 3.1934 (0.4); 3.1695 (1.1); 3.1471 (1.4); 3.1329 (2.9); 3.1175 (2.8); 3.0875 (4.3); 3.0728 (4.0); 2.9981 (0.3); 2.9532 (4.0); 2.9237 (3.7); 2.9078 (2.7); 2.8786 (2.4); 2.3501 (1.6); 2.2807 (1.4); 2.0857 (1.9); 1.9222 (1.9); 1.8047 (0.3); 1.6265 (2.7); 1.4311 (0.4); 1.4095 (0.4); 1.3220 (0.6); 1.2954 (1.1); 0.9984 (0.6); 0.9733 (0.8); 0.9182 (0.3); 0.1076 (6.6); 0.0486 (3.1); 0.0378 (70.6); 0.0271 (3.3); −0.0286 (0.5); −0.1601 (0.4) 20-17: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.3617 (0.8); 7.3537 (0.9); 7.3399 (0.9); 7.3372 (1.0); 7.3289 (1.2); 7.3254 (1.1); 7.3224 (0.9); 7.3073 (1.1); 7.2990 (7.0); 7.1882 (0.5); 7.1688 (1.8); 7.1599 (3.2); 7.1561 (3.8); 7.1507 (2.1); 7.1417 (1.8); 7.1369 (2.2); 7.1248 (3.1); 7.1079 (0.6); 7.0938 (2.7); 7.0749 (1.9); 7.0493 (0.9); 6.4302 (2.4); 5.8519 (0.9); 5.8159 (0.9); 3.8940 (0.5); 3.8826 (1.3); 3.8720 (0.5); 3.8500 (1.7); 3.8286 (0.5); 3.8192 (0.4); 3.8058 (0.4); 3.7855 (0.9); 3.7770 (1.3); 3.7507 (0.9); 3.1014 (0.6); 3.0874 (0.6); 3.0558 (1.0); 3.0422 (1.0); 2.9513 (1.0); 2.9217 (0.9); 2.9060 (0.6); 2.8765 (0.5); 2.5552 (16.0); 2.5397 (0.7); 2.3867 (11.2); 2.0442 (10.8); 1.6646 (0.5); 0.1074 (0.4); 0.0482 (0.4); 0.0375 (9.2); 0.0265 (0.3) 20-18: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.2986 (14.2); 7.1672 (1.8); 7.1400 (2.0); 7.0970 (0.5); 7.0704 (1.5); 7.0439 (1.7); 7.0356 (1.0); 7.0283 (1.2); 7.0120 (1.0); 7.0066 (1.1); 6.9855 (0.5); 6.9793 (0.5); 6.9294 (0.8); 6.8313 (1.5); 6.8232 (4.0); 6.8120 (1.2); 6.8053 (0.8); 6.7934 (1.8); 6.7848 (1.8); 6.7644 (0.6); 6.7589 (0.5); 6.5156 (2.4); 5.8450 (0.8); 5.8086 (0.9); 4.1964 (0.4); 4.1726 (1.3); 4.1488 (1.3); 4.1250 (0.5); 3.9415 (0.6); 3.9292 (1.2); 3.9179 (0.5); 3.8957 (1.5); 3.8738 (0.7); 3.8506 (16.0); 3.8054 (0.8); 3.7970 (1.2); 3.7699 (0.9); 3.0815 (0.5); 3.0674 (0.6); 3.0352 (1.0); 3.0217 (0.9); 2.9422 (0.9); 2.9119 (0.9); 2.8959 (0.5); 2.8665 (0.5); 2.5530 (13.4); 2.1390 (0.4); 2.1274 (0.5); 2.1106 (0.9); 2.0837 (6.4); 1.6128 (3.3); 1.3213 (1.7); 1.2975 (3.5); 1.2737 (1.6); 1.0606 (0.6); 1.0455 (1.7); 1.0386 (1.8); 1.0239 (1.0); 1.0170 (1.8); 1.0104 (1.7); 0.9958 (0.8); 0.8055 (0.8); 0.7906 (2.1); 0.7855 (2.0); 0.7736 (1.8); 0.7684 (2.1); 0.7517 (0.6); 0.1075 (5.2); 0.0488 (0.8); 0.0472 (0.6); 0.0381 (20.2); 0.0304 (0.5); 0.0288 (0.6); 0.0272 (0.7) 20-19: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.5404 (0.8); 7.5144 (2.0); 7.4882 (1.5); 7.4589 (0.6); 7.4436 (0.4); 7.4346 (0.5); 7.4288 (0.7); 7.4119 (2.2); 7.3859 (1.4); 7.3656 (0.7); 7.3404 (2.6); 7.3126 (1.8); 7.2990 (7.0); 7.2862 (1.4); 7.1705 (0.5); 7.1454 (2.2); 7.1201 (3.8); 7.0862 (3.4); 7.0725 (2.6); 7.0465 (1.4); 6.9468 (0.8); 6.8599 (1.3); 6.6884 (0.4); 6.6719 (2.7); 6.5230 (2.4); 6.4841 (1.4); 5.8071 (1.1); 5.7721 (1.1); 4.6322 (1.4); 4.1945 (1.0); 4.1707 (2.9); 4.1469 (3.0); 4.1231 (1.0); 3.8049 (0.3); 3.7676 (1.6); 3.7595 (1.0); 3.7412 (2.7); 3.7274 (2.0); 3.7141 (1.8); 3.6986 (1.8); 3.6747 (1.1); 3.1486 (0.9); 3.1342 (1.0); 3.1037 (1.7); 3.0889 (1.2); 2.8982 (0.9); 2.8688 (0.9); 2.8529 (0.8); 2.8236 (0.7); 2.7361 (0.5); 2.5703 (16.0); 2.3711 (13.0); 2.3441 (2.0); 2.3201 (0.5); 2.3105 (0.6); 2.2927 (0.6); 2.2778 (0.5); 2.0831 (13.4); 1.9213 (1.4); 1.6009 (0.6); 1.5761 (1.3); 1.5514 (1.1); 1.5048 (0.6); 1.4819 (0.7); 1.3192 (3.6); 1.2954 (7.2); 1.2715 (3.6); 0.0466 (0.3); 0.0359 (8.3); 0.0250 (0.4) 20-20: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.0677 (0.4); 7.6320 (0.4); 7.6238 (0.4); 7.6164 (0.4); 7.6062 (0.6); 7.6003 (0.5); 7.4443 (3.4); 7.4323 (1.9); 7.4217 (1.8); 7.4021 (1.9); 7.3906 (7.2); 7.3560 (0.4); 7.2990 (18.0); 7.2314 (0.4); 7.1992 (0.5); 7.1885 (0.4); 7.1697 (0.5); 7.1616 (0.4); 7.1449 (0.6); 7.1238 (1.0); 7.1035 (0.9); 7.0765 (2.0); 7.0482 (1.8); 7.0252 (1.2); 7.0188 (1.4); 7.0013 (1.3); 6.9961 (1.4); 6.9746 (0.6); 6.9689 (0.6); 6.9324 (0.3); 6.8461 (1.3); 6.8176 (0.9); 6.8117 (0.9); 6.7921 (1.3); 6.7694 (0.7); 6.7645 (0.7); 6.7538 (1.1); 6.6591 (2.6); 6.4720 (1.3); 6.4095 (2.2); 5.8703 (1.2); 5.8331 (1.2); 5.3382 (0.5); 4.6353 (3.0); 4.0264 (0.4); 4.0107 (0.3); 3.9800 (1.0); 3.9541 (1.4); 3.9435 (1.1); 3.9298 (0.7); 3.9175 (1.8); 3.9047 (1.2); 3.8182 (1.1); 3.8102 (1.4); 3.7824 (1.0); 3.7728 (0.7); 3.2082 (0.7); 3.1949 (0.7); 3.1634 (1.2); 3.1494 (1.1); 3.0677 (1.1); 3.0365 (1.0); 3.0234 (0.7); 2.9917 (0.6); 2.7335 (1.1); 2.5440 (16.0); 2.5205 (0.3); 2.3499 (0.8); 2.2802 (0.7); 2.1364 (0.6); 2.1261 (0.7); 2.1083 (1.2); 2.0911 (0.8); 2.0848 (1.2); 2.0627 (0.4); 1.6256 (2.1); 1.3217 (0.4); 1.2979 (0.8); 1.0672 (0.9); 1.0522 (2.2); 1.0454 (2.4); 1.0308 (1.4); 1.0236 (2.2); 1.0170 (2.2); 1.0027 (1.0); 0.8087 (1.1); 0.7938 (2.7); 0.7879 (2.6); 0.7769 (2.5); 0.7712 (2.7); 0.7548 (0.8); 0.1075 (3.9); 0.0486 (0.9); 0.0378 (23.8); 0.0269 (1.0) 20-21: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.0778 (0.3); 7.6061 (0.3); 7.4558 (0.5); 7.4468 (0.5); 7.4381 (0.8); 7.4322 (1.0); 7.4220 (1.1); 7.4021 (0.8); 7.3775 (0.5); 7.3209 (0.4); 7.2986 (22.3); 7.2882 (2.8); 7.2602 (2.9); 7.1991 (0.3); 7.1698 (0.5); 7.1466 (0.4); 7.1238 (0.9); 7.0966 (2.4); 7.0883 (3.1); 7.0765 (2.0); 7.0609 (2.0); 7.0510 (2.5); 7.0301 (2.0); 7.0236 (2.2); 7.0059 (1.3); 7.0007 (1.4); 6.9793 (0.7); 6.9737 (0.6); 6.9477 (0.3); 6.9403 (0.6); 6.8172 (0.9); 6.8107 (0.9); 6.8011 (1.8); 6.7932 (1.4); 6.7689 (0.7); 6.7635 (0.7); 6.7536 (0.8); 6.5585 (4.4); 6.5438 (0.4); 6.3155 (1.5); 5.8490 (1.1); 5.8125 (1.2); 5.3381 (0.6); 4.6352 (2.2); 3.9800 (0.5); 3.9368 (1.4); 3.9301 (1.4); 3.9026 (1.8); 3.7900 (1.4); 3.7622 (1.1); 3.7520 (0.6); 3.1428 (0.6); 3.1288 (0.6); 3.0980 (1.3); 3.0837 (1.2); 3.0069 (1.0); 2.9764 (1.0); 2.9611 (0.7); 2.9308 (0.6); 2.7365 (1.0); 2.5711 (16.0); 2.3499 (0.6); 2.2804 (0.5); 2.1524 (0.3); 2.1347 (0.6); 2.1240 (0.7); 2.1070 (1.2); 2.0846 (1.2); 2.0788 (0.7); 2.0627 (0.5); 1.9023 (1.6); 1.6174 (0.7); 1.3214 (0.4); 1.2976 (0.8); 1.0655 (1.0); 1.0503 (2.2); 1.0434 (2.4); 1.0289 (1.3); 1.0217 (2.2); 1.0152 (2.1); 1.0007 (0.9); 0.8076 (1.2); 0.7928 (2.6); 0.7870 (2.5); 0.7761 (2.4); 0.7702 (2.6); 0.7537 (0.8); 0.1069 (0.9); 0.0482 (1.1); 0.0374 (31.8); 0.0265 (1.3) 20-22: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.0730 (0.3); 7.6323 (0.4); 7.6060 (0.5); 7.6003 (0.4); 7.4561 (0.7); 7.4476 (0.6); 7.4383 (1.0); 7.4325 (1.5); 7.4221 (1.6); 7.4029 (1.2); 7.3954 (0.4); 7.3847 (0.6); 7.3779 (0.7); 7.3696 (0.6); 7.3551 (0.4); 7.3373 (2.6); 7.3093 (3.7); 7.2990 (26.0); 7.2322 (0.4); 7.1991 (0.6); 7.1800 (2.2); 7.1533 (1.6); 7.1242 (1.8); 7.1072 (0.8); 7.0800 (1.7); 7.0516 (1.7); 7.0323 (1.2); 7.0258 (1.4); 7.0086 (1.2); 7.0031 (1.4); 6.9818 (0.7); 6.9760 (0.6); 6.9445 (0.4); 6.8200 (0.9); 6.8140 (0.9); 6.7943 (1.3); 6.7720 (0.7); 6.7663 (0.7); 6.7538 (1.0); 6.5678 (2.4); 5.8514 (1.1); 5.8149 (1.1); 5.3386 (4.0); 4.6356 (3.5); 4.0265 (0.4); 3.9809 (0.7); 3.9658 (0.5); 3.9421 (1.4); 3.9237 (0.7); 3.9060 (1.9); 3.8929 (1.1); 3.7864 (1.4); 3.7587 (1.0); 3.7505 (0.6); 3.1658 (0.6); 3.1514 (0.6); 3.1210 (1.2); 3.1057 (1.2); 3.0345 (1.1); 3.0054 (1.0); 2.9902 (0.7); 2.9595 (0.6); 2.7373 (1.0); 2.5693 (16.0); 2.3504 (0.8); 2.2804 (0.7); 2.1309 (0.6); 2.1199 (0.6); 2.1029 (1.1); 2.0850 (1.6); 2.0750 (0.7); 2.0575 (0.4); 1.9025 (0.6); 1.6107 (1.7); 1.3219 (0.5); 1.2981 (1.0); 1.2919 (0.8); 1.2743 (0.4); 1.0654 (0.9); 1.0503 (2.0); 1.0434 (2.2); 1.0374 (1.4); 1.0289 (1.3); 1.0215 (2.1); 1.0149 (2.1); 1.0005 (1.0); 0.8073 (1.1); 0.7924 (2.5); 0.7863 (2.5); 0.7754 (2.3); 0.7697 (2.6); 0.7535 (0.8); 0.1074 (5.8); 0.0488 (1.1); 0.0379 (36.1); 0.0271 (1.7) 20-23: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.7077 (0.4); 7.2989 (5.5); 7.2913 (2.6); 7.1648 (1.0); 7.1391 (4.0); 7.1256 (2.2); 7.1221 (2.1); 7.0964 (1.0); 7.0703 (1.6); 7.0433 (2.7); 7.0336 (1.4); 7.0184 (1.1); 7.0125 (1.3); 6.9917 (0.5); 6.9854 (0.4); 6.8098 (0.7); 6.8021 (0.7); 6.7869 (1.2); 6.7809 (1.0); 6.7621 (0.6); 6.7563 (0.6); 6.3328 (2.6); 5.8637 (0.9); 5.8270 (1.0); 4.1729 (0.8); 4.1491 (0.8); 3.9643 (0.4); 3.9493 (1.2); 3.9428 (1.3); 3.9150 (1.7); 3.9031 (1.0); 3.8084 (1.3); 3.7809 (0.9); 3.7711 (0.4); 3.0956 (0.5); 3.0824 (0.5); 3.0503 (1.1); 3.0368 (1.0); 2.9662 (0.9); 2.9349 (0.9); 2.9207 (0.6); 2.8899 (0.5); 2.5416 (16.0); 2.3912 (11.5); 2.1415 (0.5); 2.1304 (0.5); 2.1133 (1.0); 2.0960 (0.6); 2.0845 (4.1); 1.3449 (0.5); 1.3211 (1.7); 1.3049 (3.0); 1.2974 (4.2); 1.2736 (1.2); 1.0609 (0.7); 1.0458 (1.8); 1.0390 (2.0); 1.0330 (1.1); 1.0245 (1.1); 1.0172 (1.9); 1.0105 (1.9); 0.9963 (0.9); 0.9419 (1.1); 0.9200 (3.6); 0.8968 (1.3); 0.8060 (0.9); 0.7913 (2.2); 0.7884 (2.0); 0.7853 (2.1); 0.7743 (2.0); 0.7688 (2.3); 0.7525 (0.7); 0.0381 (6.8) 20-24: ¹H-NMR(300.2 MHz, d6-DMSO): δ = 10.3120 (11.4); 9.2399 (0.5); 7.3633 (0.5); 7.3163 (3.6); 7.1855 (1.0); 7.1595 (2.8); 7.1331 (2.6); 7.1130 (4.0); 7.0943 (1.5); 7.0886 (1.7); 7.0649 (2.0); 7.0432 (1.0); 7.0378 (0.9); 6.9400 (5.2); 6.9131 (2.1); 6.8907 (1.2); 6.8858 (1.0); 6.5325 (0.9); 6.3513 (2.4); 6.3147 (2.5); 5.7781 (0.5); 4.0847 (0.4); 4.0610 (1.2); 4.0373 (1.2); 4.0136 (0.4); 3.7837 (0.6); 3.7661 (0.9); 3.7477 (2.0); 3.7293 (2.5); 3.7026 (2.0); 3.6878 (0.7); 3.6664 (0.7); 3.4157 (0.7); 3.3964 (0.8); 3.3807 (0.9); 3.3508 (11.7); 2.9358 (1.0); 2.9238 (1.1); 2.8919 (1.6); 2.8803 (1.4); 2.7623 (1.3); 2.7296 (1.2); 2.7190 (1.0); 2.6861 (0.8); 2.5858 (1.1); 2.5345 (3.0); 2.5284 (6.3); 2.5223 (8.7); 2.5163 (6.4); 2.5102 (3.2); 2.4900 (21.2); 2.2376 (16.0); 2.1048 (0.4); 2.0867 (0.8); 2.0756 (1.0); 2.0591 (1.7); 2.0419 (1.0); 2.0312 (1.0); 2.0094 (5.4); 1.3010 (0.5); 1.2657 (3.1); 1.2184 (1.5); 1.1946 (2.9); 1.1709 (1.4); 1.0763 (0.3); 1.0584 (1.1); 1.0437 (3.0); 1.0364 (3.4); 1.0307 (1.9); 1.0229 (1.9); 1.0155 (3.1); 1.0083 (3.2); 0.9951 (1.3); 0.8996 (0.9); 0.8777 (3.1); 0.8545 (1.1); 0.8121 (1.4); 0.7986 (3.5); 0.7923 (3.8); 0.7819 (3.5); 0.7753 (3.6); 0.7600 (1.1); 0.0196 (7.3) 20-28: ¹H-NMR(400.1 MHz, CDCl3): δ = 8.2581 (2.5); 8.0622 (0.5); 8.0424 (0.4); 7.5078 (0.7); 7.4881 (0.9); 7.4061 (2.7); 7.4008 (2.2); 7.3901 (3.3); 7.3704 (1.5); 7.3502 (0.8); 7.3052 (4.7); 7.2829 (3.7); 7.2610 (29.0); 7.2015 (1.2); 7.1829 (1.3); 7.1595 (1.0); 7.1321 (0.6); 7.1114 (0.7); 7.0872 (3.2); 7.0678 (1.8); 7.0464 (1.0); 7.0273 (1.2); 6.9970 (0.5); 6.9682 (3.0); 6.9523 (6.8); 6.9070 (3.1); 6.8865 (2.3); 6.8695 (0.7); 6.1766 (2.7); 5.6167 (1.5); 5.5889 (1.6); 5.3009 (0.6); 4.6747 (0.3); 4.6550 (0.4); 4.6453 (0.4); 4.5983 (0.6); 3.9882 (0.8); 3.9432 (1.0); 3.8272 (0.5); 3.8174 (0.5); 3.7989 (1.2); 3.7901 (1.3); 3.7732 (2.2); 3.7639 (2.6); 3.7572 (2.5); 3.7433 (2.2); 3.7302 (0.7); 3.7160 (0.8); 3.7084 (0.9); 3.7020 (0.9); 3.6803 (0.6); 3.6736 (0.6); 3.3927 (1.0); 3.0303 (2.6); 3.0031 (1.8); 2.9950 (1.6); 2.7660 (1.5); 2.7394 (1.5); 2.7317 (1.3); 2.7053 (1.1); 2.4274 (0.4); 2.3712 (16.0); 2.3603 (6.9); 2.3360 (0.8); 2.3124 (2.3); 2.2722 (5.9); 2.2426 (2.0); 2.1901 (0.5); 2.1746 (0.7); 2.1195 (0.4); 2.0894 (0.8); 2.0332 (15.8); 1.9824 (0.6); 1.9601 (0.5); 1.8693 (4.5); 1.7859 (0.5); 1.7227 (0.4); 1.6717 (0.4); 1.6392 (0.5); 1.6015 (0.6); 1.5817 (0.6); 1.5630 (0.6); 1.5438 (0.8); 1.4837 (0.5); 1.4734 (0.5); 1.4219 (0.6); 1.3594 (0.5); 1.2541 (5.6); 1.2253 (1.2); 1.1344 (0.4); 1.1204 (0.4); 1.1039 (0.4); 0.9961 (0.3); 0.9827 (0.3); 0.9624 (0.3); 0.8960 (0.7); 0.8796 (1.2); 0.8583 (1.9); 0.8424 (1.9); - 0.0002 (30.0) 20-31: ¹H-NMR(400.1 MHz, CDCl3): δ = 8.2278 (0.5); 7.5356 (1.2); 7.5161 (2.6); 7.4958 (1.8); 7.4163 (2.6); 7.3973 (2.1); 7.3691 (0.4); 7.3433 (0.5); 7.3209 (3.6); 7.2984 (4.9); 7.2879 (2.8); 7.2612 (21.0); 7.2002 (0.8); 7.1840 (1.0); 7.1690 (0.8); 7.1593 (1.3); 7.1326 (1.4); 7.1098 (8.7); 7.0868 (2.4); 6.7955 (1.4); 6.6549 (3.0); 6.5141 (1.5); 6.3458 (3.2); 5.7365 (1.6); 5.7088 (1.6); 3.9887 (1.3); 3.9431 (1.5); 3.8428 (0.5); 3.8339 (0.6); 3.8020 (1.5); 3.7750 (3.6); 3.7651 (4.4); 3.7556 (2.4); 3.7378 (0.7); 3.7287 (0.6); 3.1223 (1.3); 3.1147 (1.3); 3.0887 (1.7); 3.0805 (1.5); 2.8566 (1.3); 2.8329 (1.3); 2.8229 (1.2); 2.7978 (1.0); 2.3839 (16.0); 2.3119 (2.7); 2.2627 (1.4); 2.2424 (2.6); 1.8833 (0.9); 1.8412 (0.4); 1.8032 (0.4); 1.7564 (0.5); 1.6947 (0.5); 1.6731 (0.5); 1.6402 (0.5); 1.6022 (0.6); 1.5794 (0.6); 1.5430 (0.6); 1.4857 (0.4); 1.4287 (0.4); 1.2536 (2.9); 1.2082 (0.6); 0.8792 (0.5); 0.8575 (1.1); 0.8418 (1.3); −0.0002 (21.1) 20-33: ¹H-NMR(400.1 MHz, CDCl3): δ = 8.0736 (0.7); 7.5690 (0.3); 7.4113 (0.5); 7.4001 (0.7); 7.3846 (0.6); 7.3664 (0.5); 7.2876 (0.9); 7.2612 (25.2); 7.2394 (2.2); 7.2031 (3.7); 7.1715 (0.8); 7.1591 (1.1); 7.1310 (1.0); 7.1123 (1.2); 7.0859 (2.1); 7.0646 (1.7); 7.0441 (2.6); 7.0232 (1.7); 7.0006 (0.7); 6.9887 (1.1); 6.9775 (1.7); 6.9693 (1.1); 6.9606 (1.9); 6.9422 (1.2); 6.9256 (2.9); 6.9055 (2.4); 6.8699 (0.8); 6.8164 (0.4); 6.7995 (0.5); 6.7790 (1.3); 6.7590 (1.8); 6.7422 (1.2); 6.7160 (0.5); 6.2610 (1.8); 5.7603 (1.5); 5.7326 (1.6); 5.7091 (0.4); 5.3006 (0.9); 4.7249 (0.6); 4.7064 (0.6); 4.5975 (0.9); 3.9885 (1.0); 3.9430 (1.2); 3.8730 (0.6); 3.8613 (0.7); 3.8450 (1.6); 3.8341 (1.7); 3.8082 (1.8); 3.8026 (2.0); 3.7752 (1.2); 3.7554 (0.4); 3.7297 (0.4); 3.6936 (0.6); 3.6763 (1.1); 3.6683 (1.2); 3.6486 (0.9); 3.0374 (0.5); 3.0180 (0.6); 2.9813 (0.3); 2.9305 (0.9); 2.9219 (1.0); 2.8959 (1.7); 2.8874 (1.6); 2.8457 (1.7); 2.8204 (1.7); 2.8112 (1.1); 2.7857 (0.9); 2.7435 (0.4); 2.7114 (1.9); 2.5436 (16.0); 2.5248 (0.7); 2.3936 (1.8); 2.3793 (0.5); 2.3518 (0.4); 2.3320 (0.4); 2.3122 (2.3); 2.2425 (2.1); 2.1918 (0.4); 2.1741 (0.4); 2.1643 (0.4); 2.1419 (0.4); 2.0991 (0.8); 2.0808 (1.4); 2.0669 (1.8); 2.0539 (1.3); 2.0458 (1.3); 2.0321 (0.9); 2.0067 (16.0); 1.8750 (1.5); 1.8197 (0.4); 1.7885 (0.4); 1.7212 (0.4); 1.6471 (0.5); 1.6016 (0.6); 1.5628 (0.6); 1.5412 (0.7); 1.4234 (0.5); 1.3571 (0.6); 1.2536 (6.2); 1.2245 (1.2); 1.1355 (0.4); 1.1226 (0.4); 1.1062 (0.4); 1.0929 (0.4); 1.0542 (0.5); 1.0384 (1.0); 1.0262 (2.0); 1.0144 (3.2); 1.0097 (3.5); 0.9934 (3.0); 0.9889 (2.9); 0.9776 (1.4); 0.9620 (0.6); 0.9405 (0.4); 0.8796 (1.4); 0.8588 (1.9); 0.8424 (1.9); 0.7930 (0.9); 0.7688 (2.0); 0.7570 (4.1); 0.7457 (3.3); 0.7415 (3.4); 0.7292 (1.1); −0.0002 (24.8) 20-34: ¹H-NMR(400.1 MHz, CDCl3): δ = 8.2040 (1.4); 7.3983 (0.4); 7.3869 (0.4); 7.3744 (0.5); 7.3645 (0.4); 7.3545 (0.8); 7.3350 (1.4); 7.2978 (6.0); 7.2777 (4.2); 7.2611 (26.4); 7.2008 (0.6); 7.1838 (0.8); 7.1692 (0.6); 7.1594 (1.0); 7.1316 (1.6); 7.1047 (6.5); 7.0858 (2.1); 7.0514 (0.6); 7.0332 (0.5); 7.0039 (0.7); 6.9712 (2.6); 6.9518 (2.3); 6.9178 (2.4); 6.9132 (2.3); 6.8928 (1.7); 6.8293 (3.4); 6.3072 (3.5); 5.7293 (1.6); 5.7016 (1.6); 5.3016 (0.5); 3.9889 (0.9); 3.9436 (1.0); 3.8655 (0.6); 3.8557 (0.8); 3.8477 (0.7); 3.8136 (1.6); 3.8041 (1.0); 3.7868 (3.1); 3.7754 (2.7); 3.7619 (2.2); 3.7429 (0.8); 3.7348 (0.6); 3.7140 (0.5); 3.7062 (0.4); 3.6848 (0.3); 3.6782 (0.3); 3.1747 (0.4); 3.1541 (0.4); 3.1391 (0.5); 3.1213 (1.6); 3.1136 (1.3); 3.0870 (1.7); 3.0794 (1.5); 2.8537 (1.2); 2.8289 (1.3); 2.8203 (1.2); 2.7949 (1.0); 2.3886 (16.0); 2.3124 (1.8); 2.2683 (3.3); 2.2429 (1.7); 1.9643 (0.4); 1.9445 (0.5); 1.9327 (0.5); 1.9216 (0.8); 1.9090 (1.1); 1.9002 (1.3); 1.8881 (2.0); 1.8754 (1.6); 1.8673 (1.3); 1.8535 (0.8); 1.8311 (0.4); 1.7960 (0.4); 1.7858 (0.5); 1.7636 (0.6); 1.6399 (1.0); 1.6098 (1.0); 1.6010 (1.1); 1.5459 (0.9); 1.4236 (0.5); 1.2541 (3.2); 1.0460 (0.4); 1.0297 (0.8); 1.0085 (0.9); 0.9812 (3.1); 0.9767 (3.2); 0.9601 (3.1); 0.9559 (3.0); 0.9191 (0.3); 0.8800 (0.6); 0.8574 (1.2); 0.8423 (1.3); 0.7614 (0.3); 0.7491 (0.9); 0.7330 (0.9); 0.7217 (0.6); 0.6923 (3.2); 0.6869 (3.2); 0.6808 (3.2); 0.6688 (1.2); −0.0002 (27.5) 20-35: ¹H-NMR(400.1 MHz, CDCl3): δ = 8.2043 (1.0); 7.3992 (0.3); 7.3851 (0.4); 7.3660 (0.3); 7.3364 (0.9); 7.3187 (4.4); 7.2607 (24.7); 7.2018 (0.8); 7.1889 (1.1); 7.1696 (0.9); 7.1590 (1.3); 7.1511 (1.2); 7.1357 (1.6); 7.1304 (1.7); 7.1079 (10.0); 7.0865 (2.2); 7.0714 (1.4); 7.0515 (2.5); 7.0313 (1.8); 6.9963 (0.5); 6.9807 (1.5); 6.9642 (2.2); 6.9461 (1.2); 6.8675 (0.5); 6.8605 (0.4); 6.7970 (1.3); 6.7784 (2.0); 6.7611 (1.1); 6.2293 (3.4); 5.8048 (1.4); 5.7767 (1.4); 5.3005 (0.4); 4.5971 (0.4); 3.9886 (1.1); 3.9425 (1.7); 3.9246 (2.2); 3.9031 (2.9); 3.8951 (1.8); 3.8737 (0.4); 3.8631 (0.4); 3.8336 (2.0); 3.8130 (1.3); 3.7155 (0.3); 3.1812 (0.4); 3.1653 (0.5); 3.1490 (0.4); 3.0603 (1.0); 3.0546 (1.0); 3.0269 (1.8); 3.0194 (1.6); 2.9325 (1.4); 2.9068 (1.3); 2.8975 (1.0); 2.8861 (0.4); 2.8737 (0.9); 2.3926 (16.0); 2.3525 (0.3); 2.3221 (0.8); 2.3122 (2.4); 2.2912 (0.6); 2.2637 (2.8); 2.2425 (2.3); 2.1917 (0.8); 2.1614 (0.5); 2.1413 (0.5); 2.1321 (0.4); 2.1191 (0.8); 2.1042 (1.1); 2.0968 (1.2); 2.0839 (1.8); 2.0716 (1.2); 2.0626 (1.1); 2.0491 (0.7); 1.9982 (0.4); 1.9501 (0.4); 1.9261 (0.4); 1.9106 (0.5); 1.8335 (0.6); 1.7658 (0.8); 1.7482 (0.9); 1.6657 (1.4); 1.6324 (1.6); 1.6016 (1.6); 1.5854 (1.6); 1.5680 (1.6); 1.5437 (1.5); 1.5249 (1.4); 1.4225 (1.1); 1.2536 (12.6); 1.2232 (2.8); 1.2063 (2.2); 1.1688 (1.2); 1.1338 (1.0); 1.0944 (0.9); 1.0750 (1.0); 1.0585 (1.3); 1.0388 (2.0); 1.0277 (3.7); 1.0233 (3.8); 1.0067 (3.7); 1.0023 (3.6); 0.9919 (1.9); 0.9719 (1.2); 0.9513 (1.2); 0.8800 (4.0); 0.8579 (4.2); 0.8430 (3.6); 0.8164 (2.0); 0.8047 (2.1); 0.7915 (1.9); 0.7745 (2.4); 0.7612 (4.3); 0.7505 (4.0); 0.7354 (1.6); −0.0002 (26.6) 20-36: ¹H-NMR(300.2 MHz, CDCl3): δ = 7.4556 (0.5); 7.4468 (0.7); 7.4381 (0.8); 7.4291 (1.9); 7.4219 (2.8); 7.4025 (2.2); 7.3953 (0.7); 7.3844 (1.1); 7.3777 (1.2); 7.3697 (0.6); 7.3548 (0.6); 7.3077 (0.7); 7.2987 (21.2); 7.2321 (0.4); 7.2216 (0.3); 7.1998 (0.4); 7.1887 (0.4); 7.1641 (0.3); 7.1513 (0.4); 7.1381 (0.5); 7.1245 (1.4); 7.0981 (1.6); 7.0700 (2.3); 7.0455 (2.9); 7.0293 (1.9); 7.0218 (5.4); 7.0058 (3.5); 7.0011 (3.7); 6.9792 (1.3); 6.9739 (1.1); 6.8543 (1.4); 6.8319 (0.4); 6.8150 (1.0); 6.8087 (1.0); 6.7914 (1.5); 6.7671 (0.9); 6.7618 (0.7); 6.7537 (0.6); 6.6909 (0.4); 6.6549 (2.4); 6.1202 (1.9); 5.8019 (1.1); 5.7652 (1.3); 5.3379 (0.8); 4.6354 (6.9); 4.1727 (0.3); 4.1489 (0.4); 3.9811 (0.4); 3.9328 (0.4); 3.9167 (0.5); 3.8963 (1.5); 3.8807 (2.1); 3.8718 (1.8); 3.8619 (2.2); 3.8415 (0.7); 3.8258 (1.1); 3.7843 (0.8); 3.7631 (0.6); 3.7520 (0.6); 3.2837 (0.9); 3.2731 (0.9); 3.2378 (1.2); 3.2278 (1.0); 2.9408 (1.0); 2.9074 (1.1); 2.8952 (0.9); 2.8617 (0.7); 2.7391 (0.9); 2.5206 (0.9); 2.4958 (1.0); 2.4605 (16.0); 2.4064 (0.8); 2.3808 (12.1); 2.3633 (2.2); 2.3502 (0.9); 2.2814 (1.2); 2.1384 (0.4); 2.1212 (0.7); 2.1101 (0.8); 2.0922 (1.3); 2.0851 (2.1); 2.0755 (0.9); 2.0643 (0.7); 2.0472 (0.4); 1.6583 (0.9); 1.6369 (0.8); 1.6126 (0.9); 1.5946 (1.0); 1.5845 (1.0); 1.5669 (1.4); 1.5492 (0.9); 1.5396 (0.8); 1.5220 (0.5); 1.3218 (0.6); 1.2980 (1.2); 1.2742 (0.5); 1.0592 (1.3); 1.0446 (2.5); 1.0376 (2.8); 1.0232 (1.6); 1.0160 (2.5); 1.0094 (2.2); 0.9952 (1.1); 0.8477 (0.4); 0.8303 (0.9); 0.8169 (1.0); 0.8066 (2.0); 0.8003 (1.9); 0.7889 (4.0); 0.7749 (3.4); 0.7707 (3.4); 0.7615 (1.5); 0.7533 (1.4); 0.7463 (1.1); 0.7323 (1.0); 0.7154 (0.7); 0.7070 (0.7); 0.6555 (0.5); 0.6377 (0.9); 0.6236 (1.0); 0.6118 (0.7); 0.6059 (1.0); 0.5945 (0.8); 0.5781 (0.3); 0.1076 (6.1); 0.0487 (1.0); 0.0379 (25.9); 0.0271 (1.0); 0.0126 (0.4); −0.0050 (0.7); −0.0156 (0.9); −0.0330 (0.9); −0.0479 (0.6)

TABLE 33 Compounds according to formula (21)

Ex No R⁷ R⁸ Q

L—R⁶ LogP 21-01 Cl H 3-(trifluoro- methyl)phenyl

(2,4-dimethyl- phenyl)methyl 5.00^([a]) 21-02 CH₃ H 3-cyclopropyl- 2-fluorophenyl

(2,4-dimethyl- phenyl)methyl 4.69^([a]) 21-03 Cl H 3-(trifluoro- methyl)phenyl

benzyl 4.33^([a]) 21-04 Cl H 3-(trifluoro- methyl)phenyl

[4-(trifluoro- methyl)phenyl]methyl 4.62^([a]) 21-05 Cl H 3-(trifluoro- methyl)phenyl

[4-(difluoro- methoxy)phenyl]methyl 4.30^([a]) 21-06 Cl H 3-(trifluoro- methyl)phenyl

[4-(trifluoro- methoxy)phenyl]methyl 4.78^([a]) 21-07 CH₃ H 3-cyclopropyl- 2-fluorophenyl

(2,4-dimethyl- phenyl)methyl 4.74^([a]) 21-08 CH₃ H 3-cyclopropyl- 2-fluorophenyl

(2-bromo-4-methyl- phenyl)methyl 3.37^([a]) 21-09 CH₃ H 3-cyclopropyl- 2-fluorophenyl

(3,4-dichloro- phenyl)methyl 4.66^([a]) 21-10 Cl H 3-(trifluoro- methyl)phenyl

[4-(difluoro- methyl)phenyl]methyl 4.19^([a]) 21-11 CH₃ H 3-cyclopropyl- 2-fluorophenyl

[2-chloro-4-(trifluoro- methyl)phenyl]methyl 4.81^([a]) 21-12 CH₃ H 3-cyclopropyl- 2-fluorophenyl

(2-chloro-4-methyl- phenyl)methyl 4.62^([a]) 21-13 Cl H 3-(trifluoro- methyl)phenyl

(4-nitrophenyl)methyl 3.98^([a]) 21-14 Cl H 3-(trifluoro- methyl)phenyl

[4-(trifluoromethyl- thio)phenyl]methyl 5.08^([a]) 21-15 CH₃ H 3-chloro-2- fluorophenyl

(2-chloro-4-methyl- phenyl)methyl 4.51^([a]) 21-16 CH₃ H 3-cyclopropyl- 2-fluorophenyl

(2-chloro-4-methoxy- phenyl)methyl 4.36^([a]) 21-17 CH₃ H 3- (difluoromethyl) phenyl

(2-chloro-4- methylphenyl)methyl 4.13^([a]) 21-18 Cl H 3- (difluoromethyl)- 2-fluorophenyl

(2-chloro-4- methylphenyl)methyl 4.66^([a]) 21-19 CH₃ H 3-cyclopropyl- 2-fluorophenyl

[2-chloro-4- (difluoromethyl)phenyl] methyl 4.40^([a]) 21-20 CH₃ H 3-cyclopropyl- 2-fluorophenyl

[2-chloro-4- (difluoromethoxy)phenyl] methyl 4.47^([a]) 21-21 CH₃ H 3-cyclopropyl- 2-fluorophenyl

[2-chloro-4- (trifluoromethoxy) phenyl]methyl 5.08^([a]) 21-22 CH₃ H 3-cyclopropyl- 2-fluorophenyl

(3-bromo-5- methylphenyl)methyl 4.84^([a]) 21-23 CH₃ H 3-cyclopropyl- 2-fluorophenyl

(2-bromo-4- methylphenyl)methyl 4.84^([a]) 21-24 CH₃ H 3-cyclopropyl- 2-fluorophenyl

(4-bromo-2- methylphenyl)methyl 4.85^([a]) 21-25 Cl H 3- cyclopropylphenyl

(2,4- dimethylphenyl)methyl 5.19^([a]) 21-26 Cl H 3-cyclopropyl- 2-fluorophenyl

(2,4- dimethylphenyl)methyl 5.23^([a]) 21-27 Cl H 3- (difluoromethyl)phenyl

(2,4- dimethylphenyl)methyl 4.53^([a]) 21-28 Cl H 3-bromophenyl

(2,4- dimethylphenyl)methyl 5.00^([a]) 21-29 Cl H 3-chlorophenyl

(2,4- dimethylphenyl)methyl 4.90^([a]) 21-30 Cl H 3- (difluoromethyl) phenyl

(2-bromo-4- methylphenyl)methyl 4.62^([a]) 21-31 CH₃ H 2-fluoro-3- (trifluoromethyl) phenyl

(2,4- dimethylphenyl)methyl 4.56^([a]) 21-32 Cl H 3-cyclopropyl- 2-fluorophenyl

(4-bromo-2- methylphenyl)methyl 5.32^([a]) 21-33 Cl H 3- cyclopropylphenyl

(2-bromo-4- methylphenyl)methyl 5.28^([a]) 21-34 Cl H 3-cyclopropyl- 2-fluorophenyl

(2-bromo-4- methylphenyl)methyl 5.31^([a]) 21-35 CH₃ H 3-cyclopropyl- 2-fluorophenyl

(2-cyclopropyl-4- methylphenyl)methyl 5.08^([a]) In table 33, ″#″ denotes the point of attachment to the L—R⁶ group and ″*″ denotes the point of attachment to the pyridazin-4-yl group.

TABLE 34 21-01: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.2680 (8.8); 8.0465 (1.1); 8.0311 (1.0); 7.6522 (0.5); 7.6349 (3.2); 7.6313 (2.4); 7.6260 (4.8); 7.6244 (5.2); 7.6185 (0.4); 7.6158 (0.4); 7.5084 (2.6); 7.4628 (0.4); 7.4544 (1.1); 7.4493 (1.2); 7.4463 (1.5); 7.4425 (1.5); 7.4365 (1.1); 7.4313 (0.7); 7.2577 (5.2); 7.0422 (2.6); 7.0269 (3.0); 6.9595 (3.0); 6.8715 (1.8); 6.8562 (1.4); 5.2958 (1.1); 4.6896 (0.4); 4.6817 (0.7); 4.6756 (1.0); 4.6678 (1.0); 4.6599 (0.9); 4.6536 (0.6); 3.8303 (1.4); 3.8223 (1.4); 3.8076 (2.0); 3.7996 (1.8); 3.7126 (2.2); 3.7071 (2.1); 3.6900 (1.5); 3.6844 (1.4); 3.0690 (0.5); 3.0551 (0.7); 3.0411 (2.3); 3.0305 (2.9); 3.0146 (2.1); 3.0030 (0.4); 2.9866 (0.4); 2.3588 (16.0); 2.2554 (14.7); 1.5535 (4.3); 0.0059 (0.5); −0.0002 (5.9) 21-02: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.2238 (0.8); 8.1980 (0.8); 8.1207 (5.3); 7.2986 (7.3); 7.1850 (0.4); 7.1663 (1.9); 7.1643 (1.9); 7.1581 (2.8); 7.1405 (4.0); 7.1192 (1.9); 7.0937 (2.3); 6.9889 (2.3); 6.9151 (1.3); 6.8871 (1.7); 6.8729 (1.2); 6.8586 (0.9); 6.8416 (0.5); 4.7282 (0.5); 4.7154 (0.6); 4.7032 (0.7); 4.6915 (0.6); 4.6783 (0.5); 3.8621 (0.8); 3.8480 (0.9); 3.8246 (1.6); 3.8106 (1.5); 3.7412 (1.6); 3.7312 (1.6); 3.7037 (0.9); 3.6937 (0.9); 3.0852 (3.4); 3.0604 (3.4); 2.7425 (16.0); 2.4135 (12.0); 2.2895 (11.2); 2.1836 (0.5); 2.1724 (0.6); 2.1555 (1.0); 2.1382 (0.6); 2.1272 (0.6); 2.0456 (1.4); 1.6084 (6.1); 1.1004 (0.7); 1.0854 (1.8); 1.0785 (2.0); 1.0639 (1.1); 1.0568 (1.9); 1.0502 (1.8); 1.0357 (0.8); 0.8491 (0.9); 0.8341 (2.2); 0.8287 (2.1); 0.8172 (1.9); 0.8119 (2.3); 0.7953 (0.7); 0.0382 (9.0); 0.0273 (0.4) 21-03: ¹H-NMR(499.9 MHz, CDCl3): δ = 8.2630 (16.0); 7.9631 (1.8); 7.9477 (1.8); 7.6317 (8.3); 7.6214 (9.6); 7.6058 (0.5); 7.4670 (4.9); 7.4382 (0.4); 7.4302 (1.8); 7.4253 (2.0); 7.4206 (2.9); 7.4169 (2.6); 7.4121 (2.0); 7.4071 (1.5); 7.3996 (0.4); 7.2586 (11.5); 7.2368 (5.8); 7.2315 (39.9); 7.2113 (1.6); 7.2049 (0.6); 7.2008 (0.4); 4.7304 (0.4); 4.7236 (0.5); 4.7216 (0.6); 4.7150 (1.3); 4.7082 (1.6); 4.6998 (1.7); 4.6927 (1.6); 4.6859 (1.4); 4.6793 (0.7); 4.6704 (0.4); 3.7932 (2.5); 3.7842 (2.5); 3.7706 (3.8); 3.7615 (3.8); 3.6839 (4.0); 3.6775 (4.2); 3.6612 (2.8); 3.6549 (2.8); 3.1202 (1.7); 3.1069 (1.8); 3.0926 (3.8); 3.0793 (3.8); 3.0509 (4.0); 3.0353 (4.0); 3.0234 (2.0); 3.0077 (1.9); 1.5508 (5.7); 0.0061 (0.5); −0.0002 (13.9); −0.0064 (0.9) 21-04: ¹H-NMR(300.2 MHz, CDCl3): δ =8.3083 (16.0); 8.0825 (1.8); 8.0562 (1.8); 7.6838 (8.2); 7.6664 (8.1); 7.6445 (0.4); 7.6398 (0.5); 7.5770 (5.5); 7.5499 (11.8); 7.4807 (0.5); 7.4678 (1.9); 7.4596 (2.0); 7.4507 (2.8); 7.4438 (2.9); 7.4319 (8.4); 7.4053 (5.4); 7.2985 (34.4); 5.3383 (0.4); 4.8199 (0.5); 4.8026 (1.0); 4.7929 (1.4); 4.7797 (1.5); 4.7665 (1.4); 4.7559 (1.0); 4.7438 (0.6); 4.7300 (0.4); 3.8470 (2.1); 3.8331 (2.1); 3.8086 (3.6); 3.7947 (3.4); 3.6961 (4.0); 3.6862 (4.0); 3.6578 (2.6); 3.6479 (2.5); 3.2495 (0.9); 3.2268 (1.0); 3.2038 (3.0); 3.1818 (3.0); 3.1682 (3.5); 3.1411 (3.2); 3.1224 (1.1); 3.0955 (1.0); 1.7032 (3.3); 1.2940 (0.7); 0.1072 (1.5); 0.0483 (1.6); 0.0374 (46.8); 0.0266 (2.0) 21-05: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.3108 (6.7); 8.0600 (0.9); 8.0338 (0.9); 7.6840 (3.3); 7.6668 (4.5); 7.5469 (2.2); 7.4823 (0.9); 7.4736 (0.9); 7.4666 (1.2); 7.4601 (1.1); 7.4517 (0.8); 7.4435 (0.6); 7.2988 (21.6); 7.2701 (4.6); 7.0663 (4.1); 7.0382 (3.3); 6.7470 (1.6); 6.5015 (3.3); 6.2561 (1.6); 5.3387 (3.6); 4.7491 (0.5); 4.7376 (0.7); 4.7247 (0.7); 4.7127 (0.7); 4.7016 (0.5); 3.8376 (1.0); 3.8236 (1.0); 3.7993 (1.7); 3.7853 (1.7); 3.7062 (1.8); 3.6963 (1.9); 3.6682 (1.1); 3.6583 (1.0); 3.1664 (0.5); 3.1442 (0.5); 3.1202 (1.7); 3.0984 (1.7); 3.0854 (1.9); 3.0583 (1.7); 3.0389 (0.6); 3.0122 (0.6); 1.5895 (16.0); 1.2916 (0.5); 0.1068 (4.2); 0.0479 (0.8); 0.0371 (21.2); 0.0264 (0.9) 21-06: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.3091 (13.7); 8.0732 (1.4); 8.0471 (1.4); 7.6826 (5.9); 7.6653 (7.0); 7.5473 (3.4); 7.4925 (0.3); 7.4808 (1.4); 7.4716 (1.5); 7.4640 (2.2); 7.4578 (2.0); 7.4538 (1.0); 7.4500 (1.3); 7.4418 (1.0); 7.3345 (5.8); 7.3056 (8.5); 7.2985 (21.2); 7.1617 (5.2); 7.1354 (3.8); 5.3378 (3.5); 4.7745 (0.4); 4.7612 (0.8); 4.7510 (1.1); 4.7472 (1.0); 4.7378 (1.1); 4.7290 (1.0); 4.7248 (1.1); 4.7154 (0.8); 4.7014 (0.4); 3.8424 (1.6); 3.8285 (1.6); 3.8042 (2.8); 3.7903 (2.6); 3.7061 (3.1); 3.6962 (3.2); 3.6679 (1.9); 3.6580 (1.8); 3.1868 (0.8); 3.1646 (0.8); 3.1405 (2.6); 3.1186 (2.7); 3.1066 (3.0); 3.0793 (2.7); 3.0605 (0.9); 3.0334 (0.9); 1.5924 (16.0); 0.1073 (3.7); 0.0478 (0.9); 0.0370 (22.2); 0.0261 (0.9) 21-07: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.2229 (0.8); 8.1964 (0.8); 8.1204 (5.3); 7.2983 (12.0); 7.1847 (0.4); 7.1663 (1.9); 7.1639 (1.8); 7.1578 (2.8); 7.1402 (4.0); 7.1191 (1.8); 7.0936 (2.3); 6.9890 (2.2); 6.9149 (1.3); 6.8940 (1.2); 6.8873 (1.7); 6.8729 (1.2); 6.8585 (0.9); 6.8419 (0.5); 5.3377 (0.9); 4.7282 (0.5); 4.7168 (0.6); 4.7031 (0.7); 4.6913 (0.7); 4.6780 (0.5); 3.8619 (0.9); 3.8478 (0.9); 3.8243 (1.6); 3.8103 (1.5); 3.7409 (1.6); 3.7309 (1.6); 3.7033 (0.9); 3.6934 (0.9); 3.0852 (3.4); 3.0604 (3.4); 2.7424 (16.0); 2.4134 (11.8); 2.3384 (0.4); 2.2894 (11.0); 2.1834 (0.5); 2.1724 (0.6); 2.1551 (1.0); 2.1377 (0.6); 2.1268 (0.6); 1.6010 (2.0); 1.1001 (0.7); 1.0852 (1.8); 1.0782 (2.0); 1.0636 (1.1); 1.0566 (1.9); 1.0499 (1.8); 1.0354 (0.9); 0.8488 (0.9); 0.8340 (2.2); 0.8289 (2.1); 0.8169 (1.9); 0.8118 (2.3); 0.7951 (0.7); 0.1079 (0.8); 0.0488 (0.5); 0.0380 (15.4); 0.0272 (0.6) 21-08: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.0957 (5.6); 8.0600 (0.8); 7.3333 (2.4); 7.2990 (10.0); 7.1910 (2.1); 7.1653 (2.7); 7.1409 (3.6); 7.1229 (2.8); 7.1185 (2.1); 7.1137 (1.8); 7.0955 (0.4); 6.9527 (1.4); 6.9293 (1.1); 6.8816 (0.7); 6.8651 (1.0); 6.8598 (0.9); 6.8505 (1.2); 6.8365 (0.6); 6.8278 (0.6); 5.3379 (0.4); 4.5903 (0.4); 4.5780 (0.6); 4.5674 (0.6); 4.5552 (0.6); 4.5434 (0.4); 3.9217 (0.4); 3.8907 (0.9); 3.8388 (0.8); 3.8243 (0.8); 3.8029 (0.4); 3.7863 (0.4); 3.2302 (0.5); 3.2086 (0.6); 3.1835 (1.4); 3.1620 (1.3); 3.1302 (1.4); 3.1021 (1.4); 3.0838 (0.6); 3.0556 (0.6); 2.7278 (16.0); 2.6123 (0.5); 2.2684 (11.6); 2.1674 (0.5); 2.1564 (0.6); 2.1392 (1.0); 2.1223 (0.6); 2.1109 (0.6); 1.6168 (0.5); 1.0980 (0.6); 1.0825 (1.9); 1.0760 (2.0); 1.0613 (1.1); 1.0541 (2.0); 1.0475 (1.9); 1.0332 (0.8); 0.8421 (0.9); 0.8271 (2.3); 0.8213 (2.3); 0.8103 (2.1); 0.8044 (2.4); 0.7883 (0.7); 0.1074 (2.7); 0.0484 (0.5); 0.0376 (14.2); 0.0269 (0.7) 21-09: ¹H-NMR(300.2 MHz, d₆-DMSO): δ = 7.6095 (1.1); 7.5577 (0.5); 7.5514 (0.5); 7.3941 (0.4); 7.3667 (0.7); 7.2957 (0.4); 7.2891 (0.3); 7.1466 (0.4); 5.7760 (1.7); 3.3407 (16.0); 2.6006 (2.7); 2.5349 (0.6); 2.5289 (1.3); 2.5229 (1.8); 2.5168 (1.3); 2.5109 (0.6); 1.0502 (0.3); 1.0428 (0.4); 1.0220 (0.4); 1.0148 (0.4); 0.8035 (0.4); 0.7970 (0.4); 0.7865 (0.4); 0.7798 (0.4); 0.0212 (1.0) 21-10: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.3056 (16.0); 8.2808 (1.1); 8.0621 (1.9); 8.0357 (1.9); 7.6823 (7.9); 7.6651 (9.3); 7.6394 (0.4); 7.5777 (0.6); 7.5373 (4.7); 7.5046 (0.4); 7.4998 (0.4); 7.4825 (0.7); 7.4670 (2.6); 7.4589 (5.8); 7.4520 (4.9); 7.4454 (3.4); 7.4305 (10.4); 7.3944 (10.0); 7.3671 (4.2); 7.2987 (16.0); 6.8163 (2.7); 6.6283 (5.7); 6.4404 (2.8); 5.3374 (4.6); 4.8160 (0.3); 4.8027 (0.5); 4.7903 (1.0); 4.7793 (1.5); 4.7663 (1.6); 4.7530 (1.5); 4.7426 (1.1); 4.7302 (0.6); 4.7164 (0.4); 3.8430 (2.1); 3.8288 (2.1); 3.8047 (3.7); 3.7906 (3.5); 3.7040 (4.1); 3.6939 (4.0); 3.6658 (2.5); 3.6557 (2.4); 3.2275 (0.9); 3.2058 (0.9); 3.1822 (2.9); 3.1598 (3.0); 3.1483 (3.3); 3.1214 (3.0); 3.1025 (1.0); 3.0757 (0.9); 1.6025 (2.4); 1.2969 (0.5); 0.1081 (2.3); 0.0481 (0.7); 0.0466 (0.5); 0.0374 (22.2); 0.0282 (0.8); 0.0265 (0.9) 21-11: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1805 (0.7); 8.1530 (0.8); 8.0622 (5.2); 7.6909 (1.1); 7.6441 (2.1); 7.5427 (0.4); 7.5199 (1.0); 7.5157 (1.0); 7.4846 (1.3); 7.4747 (1.0); 7.4476 (2.6); 7.4299 (1.9); 7.4252 (1.8); 7.4024 (0.6); 7.3986 (0.6); 7.2991 (12.7); 7.1876 (0.4); 7.1693 (2.2); 7.1610 (2.1); 7.1571 (1.8); 7.1442 (3.8); 7.1189 (0.3); 6.8998 (0.7); 6.8913 (0.7); 6.8776 (1.2); 6.8649 (0.8); 6.8606 (0.6); 6.8458 (0.5); 5.3376 (0.6); 4.9651 (0.4); 4.9531 (0.6); 4.9396 (0.6); 4.9264 (0.6); 4.9156 (0.4); 3.9478 (1.0); 3.9337 (1.0); 3.9096 (1.5); 3.8956 (1.5); 3.7731 (1.5); 3.7626 (1.6); 3.7424 (0.4); 3.7352 (1.2); 3.7245 (1.2); 3.7158 (0.9); 3.6918 (1.0); 3.6717 (0.4); 3.5710 (0.5); 3.5523 (1.3); 3.5276 (1.4); 3.5175 (0.6); 3.5075 (0.4); 3.3189 (1.7); 3.3101 (1.7); 3.2924 (1.9); 3.2875 (1.9); 3.1620 (0.3); 3.1158 (0.6); 3.0970 (0.6); 3.0096 (0.5); 2.9860 (0.5); 2.9634 (0.4); 2.9420 (0.4); 2.7356 (16.0); 2.1965 (0.3); 2.1794 (0.6); 2.1682 (0.6); 2.1511 (1.1); 2.1339 (0.7); 2.1228 (0.7); 2.1059 (0.4); 1.1068 (0.7); 1.0925 (1.5); 1.0852 (1.9); 1.0788 (1.1); 1.0707 (1.1); 1.0638 (1.6); 1.0569 (1.8); 1.0425 (1.0); 0.8467 (0.9); 0.8321 (2.0); 0.8255 (2.0); 0.8149 (1.9); 0.8098 (2.1); 0.7934 (0.8); 0.1076 (3.3); 0.0483 (0.6); 0.0374 (18.2); 0.0266 (1.0) 21-12: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1231 (0.7); 8.0963 (0.8); 8.0838 (5.4); 7.2986 (13.3); 7.2337 (0.5); 7.2011 (2.1); 7.1860 (0.6); 7.1744 (4.1); 7.1679 (4.0); 7.1585 (2.8); 7.1405 (3.9); 7.1135 (0.4); 7.0685 (0.3); 6.9575 (1.2); 6.9540 (1.2); 6.9314 (1.0); 6.8963 (0.7); 6.8880 (0.7); 6.8734 (1.1); 6.8638 (0.7); 6.8588 (1.0); 6.8422 (0.5); 5.3370 (9.4); 4.8993 (0.4); 4.8865 (0.6); 4.8744 (0.7); 4.8621 (0.6); 4.8488 (0.5); 3.9338 (1.0); 3.9196 (1.0); 3.8961 (1.6); 3.8819 (1.5); 3.7581 (1.5); 3.7472 (1.6); 3.7204 (1.1); 3.7095 (1.0); 3.6604 (0.4); 3.6490 (0.4); 3.5378 (0.3); 3.5173 (0.5); 3.4820 (0.4); 3.2082 (2.0); 3.2031 (2.0); 3.1818 (2.3); 2.7298 (16.0); 2.3482 (2.6); 2.2960 (10.8); 2.1820 (0.5); 2.1707 (0.5); 2.1538 (1.0); 2.1365 (0.6); 2.1256 (0.5); 1.6208 (3.8); 1.2970 (0.4); 1.1013 (0.7); 1.0865 (1.7); 1.0794 (1.9); 1.0648 (1.0); 1.0578 (1.8); 1.0512 (1.7); 1.0366 (0.9); 0.8501 (0.9); 0.8352 (2.1); 0.8298 (1.9); 0.8183 (1.8); 0.8128 (2.2); 0.7964 (0.7); 0.1080 (4.5); 0.0490 (0.6); 0.0383 (18.9); 0.0306 (0.6); 0.0289 (0.6); 0.0274 (0.7) 21-13: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.2968 (16.0); 8.2877 (0.9); 8.2095 (1.2); 8.2015 (8.6); 8.1952 (3.2); 8.1789 (3.2); 8.1724 (9.7); 8.1363 (1.8); 8.1098 (1.8); 7.6874 (7.1); 7.6700 (8.5); 7.6446 (0.6); 7.5522 (4.0); 7.5026 (8.7); 7.4866 (2.5); 7.4736 (9.2); 7.4647 (3.4); 7.4571 (1.7); 7.4486 (1.2); 7.2990 (23.7); 5.3380 (0.7); 4.8694 (0.3); 4.8572 (0.5); 4.8424 (0.9); 4.8329 (1.4); 4.8198 (1.5); 4.8065 (1.4); 4.7974 (0.9); 4.7930 (0.8); 4.7825 (0.6); 4.7704 (0.4); 3.8673 (2.1); 3.8542 (2.2); 3.8286 (3.2); 3.8157 (3.0); 3.6878 (3.6); 3.6782 (3.6); 3.6491 (2.4); 3.6395 (2.4); 3.2991 (0.9); 3.2764 (1.0); 3.2533 (3.2); 3.2307 (3.5); 3.2226 (3.9); 3.1954 (3.3); 3.1769 (1.0); 3.1494 (1.0); 2.0829 (1.2); 1.5943 (12.8); 1.3207 (0.5); 1.2969 (1.0); 1.2732 (0.3); 0.1193 (0.4); 0.1072 (9.1); 0.0951 (0.4); 0.0479 (1.2); 0.0371 (32.3); 0.0261 (1.3) 21-14: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.3023 (12.6); 8.0931 (1.6); 8.0664 (1.6); 7.6855 (6.2); 7.6684 (7.1); 7.6442 (0.4); 7.6104 (5.7); 7.5836 (7.0); 7.5522 (3.7); 7.4808 (1.5); 7.4715 (1.5); 7.4637 (2.2); 7.4575 (1.9); 7.4501 (1.3); 7.4420 (1.0); 7.3720 (7.8); 7.3449 (6.1); 7.2987 (22.1); 5.3380 (2.8); 4.8075 (0.4); 4.7929 (0.8); 4.7832 (1.2); 4.7706 (1.2); 4.7573 (1.1); 4.7470 (0.8); 4.7342 (0.5); 3.8505 (1.6); 3.8369 (1.7); 3.8122 (2.8); 3.7987 (2.7); 3.7038 (3.0); 3.6940 (3.1); 3.6654 (1.9); 3.6556 (1.8); 3.2150 (0.8); 3.1934 (0.8); 3.1693 (2.8); 3.1472 (3.0); 3.1389 (3.3); 3.1117 (2.9); 3.0930 (0.9); 3.0658 (0.8); 1.5896 (16.0); 1.2936 (0.4); 0.1075 (2.0); 0.0483 (1.2); 0.0375 (30.2); 0.0283 (0.9); 0.0266 (1.1) 21-15: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.0953 (5.2); 7.9718 (0.8); 7.9462 (0.8); 7.4471 (0.7); 7.4413 (0.7); 7.4256 (0.8); 7.4201 (1.4); 7.4147 (1.0); 7.3996 (0.8); 7.3931 (0.9); 7.3320 (0.6); 7.3262 (0.6); 7.3107 (0.7); 7.2987 (10.8); 7.2834 (1.3); 7.2770 (1.0); 7.2541 (1.5); 7.2498 (1.3); 7.2277 (1.5); 7.2227 (1.6); 7.1967 (2.6); 7.1710 (2.9); 7.1566 (2.5); 6.9724 (1.4); 6.9471 (1.2); 4.8983 (0.5); 4.8863 (0.7); 4.8737 (0.7); 4.8603 (0.7); 4.8487 (0.5); 3.9378 (1.0); 3.9236 (1.0); 3.9001 (1.6); 3.8859 (1.5); 3.7658 (1.6); 3.7552 (1.6); 3.7280 (1.1); 3.7174 (1.1); 3.2752 (0.5); 3.2486 (0.5); 3.2288 (1.5); 3.2023 (1.6); 3.1902 (1.6); 3.1672 (1.5); 3.1438 (0.5); 3.1208 (0.4); 2.7387 (16.0); 2.2996 (11.9); 2.0838 (0.4); 1.6009 (13.1); 1.3441 (0.4); 1.3034 (2.7); 1.2735 (0.3); 0.9409 (0.9); 0.9192 (2.7); 0.8960 (1.1); 0.0478 (0.5); 0.0371 (13.2); 0.0278 (0.6); 0.0263 (0.6) 21-16: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1355 (0.6); 8.1089 (0.6); 8.0898 (4.6); 7.2990 (8.4); 7.2282 (2.0); 7.1999 (2.4); 7.1747 (1.2); 7.1660 (1.7); 7.1609 (2.5); 7.1472 (1.4); 7.1419 (2.1); 7.1146 (0.4); 6.9122 (2.2); 6.9035 (2.4); 6.8948 (0.7); 6.8874 (0.7); 6.8715 (0.9); 6.8617 (0.7); 6.8547 (0.6); 6.8408 (0.5); 6.7208 (1.3); 6.7121 (1.2); 6.6926 (1.2); 6.6838 (1.1); 5.3375 (5.4); 4.8809 (0.4); 4.8680 (0.5); 4.8557 (0.6); 4.8431 (0.5); 4.8301 (0.4); 3.9287 (0.8); 3.9146 (0.8); 3.8910 (1.3); 3.8769 (1.2); 3.8064 (0.4); 3.7798 (16.0); 3.7660 (0.4); 3.7497 (1.3); 3.7389 (1.3); 3.7120 (0.9); 3.7011 (0.9); 3.1808 (1.6); 3.1717 (1.6); 3.1555 (1.6); 3.1480 (1.6); 2.7331 (13.7); 2.1800 (0.4); 2.1686 (0.4); 2.1517 (0.8); 2.1345 (0.5); 2.1234 (0.4); 2.0835 (0.6); 1.6051 (5.9); 1.2972 (0.5); 1.0976 (0.6); 1.0824 (1.5); 1.0755 (1.7); 1.0697 (0.9); 1.0608 (0.9); 1.0538 (1.6); 1.0470 (1.5); 1.0326 (0.8); 0.8468 (0.8); 0.8318 (1.8); 0.8256 (1.8); 0.8148 (1.6); 0.8090 (1.9); 0.7927 (0.6); 0.1075 (0.8); 0.0483 (0.4); 0.0374 (11.6); 0.0266 (0.4) 21-17: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1059 (5.6); 8.0924 (0.9); 7.6316 (0.6); 7.6055 (1.6); 7.5793 (1.2); 7.5095 (1.4); 7.4839 (0.9); 7.4176 (1.9); 7.3996 (1.2); 7.3964 (1.2); 7.3926 (1.0); 7.3730 (0.8); 7.3696 (0.9); 7.3657 (0.8); 7.2988 (2.4); 7.1805 (2.0); 7.1553 (4.4); 6.9634 (1.3); 6.9606 (1.3); 6.9375 (1.0); 6.9345 (1.0); 6.9222 (1.2); 6.7344 (2.2); 6.5466 (1.1); 5.3335 (10.6); 4.8996 (0.4); 4.8881 (0.6); 4.8751 (0.7); 4.8618 (0.6); 4.8506 (0.5); 3.9341 (1.0); 3.9201 (1.0); 3.8963 (1.5); 3.8824 (1.5); 3.7604 (1.6); 3.7499 (1.6); 3.7226 (1.1); 3.7121 (1.0); 3.2693 (0.5); 3.2429 (0.5); 3.2231 (1.4); 3.1968 (1.4); 3.1732 (1.4); 3.1501 (1.4); 3.1270 (0.6); 3.1039 (0.5); 2.7354 (16.0); 2.3400 (0.4); 2.3315 (0.3); 2.2929 (11.0); 0.0358 (3.2) 21-18: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.2516 (8.2); 8.1521 (0.4); 7.9205 (1.1); 7.8941 (1.1); 7.6641 (0.8); 7.6406 (1.5); 7.6187 (0.9); 7.5383 (0.7); 7.5139 (1.6); 7.4901 (1.1); 7.4407 (1.7); 7.4138 (2.1); 7.3871 (0.8); 7.2986 (3.3); 7.1914 (2.8); 7.1650 (4.2); 7.1581 (3.6); 7.1401 (1.6); 6.9821 (2.0); 6.9576 (4.5); 6.7756 (1.5); 5.3354 (16.0); 4.9066 (0.3); 4.8934 (0.6); 4.8811 (0.9); 4.8686 (0.9); 4.8554 (0.9); 4.8442 (0.7); 4.8311 (0.4); 4.3608 (1.1); 3.9397 (1.3); 3.9257 (1.3); 3.9017 (2.1); 3.8878 (2.0); 3.7684 (2.1); 3.7579 (2.1); 3.7305 (1.5); 3.7200 (1.4); 3.2923 (0.9); 3.2653 (0.8); 3.2460 (1.9); 3.2190 (1.9); 3.1763 (1.8); 3.1537 (1.9); 3.1302 (0.9); 3.1074 (0.8); 2.3400 (0.8); 2.2951 (15.9); 1.6225 (3.9); 0.0366 (4.4) 21-19: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1689 (0.8); 8.1423 (0.8); 8.0647 (5.2); 7.5246 (2.0); 7.4359 (1.3); 7.4097 (2.0); 7.3124 (1.4); 7.2988 (10.6); 7.2882 (1.0); 7.1878 (0.4); 7.1692 (2.3); 7.1611 (2.2); 7.1571 (1.8); 7.1441 (3.8); 6.8988 (0.7); 6.8901 (0.7); 6.8764 (1.2); 6.8637 (0.8); 6.8593 (0.6); 6.8449 (0.5); 6.7775 (1.1); 6.5901 (2.2); 6.4028 (1.1); 5.3377 (1.2); 4.9565 (0.4); 4.9439 (0.6); 4.9310 (0.6); 4.9177 (0.6); 4.9061 (0.4); 3.9447 (1.0); 3.9306 (1.0); 3.9066 (1.5); 3.8926 (1.5); 3.7699 (1.5); 3.7593 (1.5); 3.7319 (1.1); 3.7213 (1.0); 3.2983 (1.6); 3.2910 (1.6); 3.2699 (2.0); 2.7492 (0.4); 2.7331 (16.0); 2.1817 (0.5); 2.1705 (0.5); 2.1534 (1.0); 2.1361 (0.6); 2.1252 (0.5); 2.0836 (1.1); 1.6023 (7.9); 1.3210 (0.4); 1.2972 (0.9); 1.1071 (0.7); 1.0926 (1.6); 1.0854 (2.0); 1.0791 (1.1); 1.0709 (1.1); 1.0639 (1.7); 1.0570 (1.8); 1.0427 (0.9); 0.9190 (0.3); 0.8490 (0.9); 0.8343 (2.1); 0.8314 (1.9); 0.8281 (2.0); 0.8172 (1.9); 0.8119 (2.1); 0.7955 (0.7); 0.1072 (3.8); 0.0479 (0.5); 0.0371 (14.4); 0.0262 (0.6) 21-20: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1518 (0.8); 8.1255 (0.8); 8.0749 (5.3); 7.3293 (2.3); 7.2991 (10.5); 7.1924 (0.5); 7.1745 (3.1); 7.1685 (3.9); 7.1462 (3.8); 7.1191 (0.4); 6.9571 (1.2); 6.9488 (1.2); 6.9291 (1.1); 6.9209 (1.0); 6.8980 (0.7); 6.8896 (0.8); 6.8754 (1.2); 6.8661 (0.7); 6.8608 (1.0); 6.8442 (0.5); 6.7258 (1.5); 6.4819 (3.2); 6.2380 (1.6); 5.3377 (1.5); 4.9136 (0.4); 4.9014 (0.6); 4.8887 (0.6); 4.8753 (0.6); 4.8636 (0.5); 3.9377 (1.0); 3.9236 (1.0); 3.8997 (1.5); 3.8858 (1.4); 3.7622 (1.5); 3.7515 (1.5); 3.7242 (1.0); 3.7136 (1.0); 3.2348 (2.0); 3.2273 (2.0); 3.2086 (2.2); 3.2042 (2.2); 2.7360 (16.0); 2.1792 (0.5); 2.1682 (0.6); 2.1510 (1.0); 2.1339 (0.6); 2.1230 (0.5); 1.6046 (6.7); 1.1052 (0.7); 1.0906 (1.6); 1.0835 (2.0); 1.0690 (1.1); 1.0619 (1.7); 1.0552 (1.8); 1.0408 (0.9); 0.8475 (1.0); 0.8327 (2.1); 0.8301 (2.0); 0.8264 (2.1); 0.8157 (1.9); 0.8101 (2.2); 0.7940 (0.7); 0.1073 (0.5); 0.0480 (0.4); 0.0372 (12.3); 0.0263 (0.5) 21-21: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1740 (0.8); 8.1470 (0.9); 8.0704 (5.3); 7.3689 (2.4); 7.3406 (2.8); 7.2988 (13.8); 7.2694 (1.8); 7.2646 (1.8); 7.1920 (0.4); 7.1733 (1.6); 7.1640 (2.7); 7.1461 (3.8); 7.1188 (0.4); 7.0539 (1.1); 7.0496 (1.0); 7.0259 (0.9); 6.8979 (0.7); 6.8896 (0.8); 6.8753 (1.2); 6.8659 (0.7); 6.8605 (1.1); 6.8438 (0.6); 5.3381 (1.0); 4.9282 (0.5); 4.9154 (0.7); 4.9029 (0.7); 4.8898 (0.7); 4.8774 (0.5); 3.9419 (1.0); 3.9279 (1.0); 3.9038 (1.5); 3.8900 (1.4); 3.7649 (1.5); 3.7544 (1.5); 3.7268 (1.0); 3.7164 (1.0); 3.2546 (2.0); 3.2473 (2.1); 3.2281 (2.3); 3.2242 (2.4); 2.7369 (16.0); 2.1796 (0.5); 2.1681 (0.6); 2.1514 (1.0); 2.1343 (0.6); 2.1233 (0.6); 2.0838 (0.6); 1.5965 (7.4); 1.3210 (0.4); 1.2974 (1.2); 1.1046 (0.7); 1.0899 (1.8); 1.0829 (2.0); 1.0683 (1.1); 1.0613 (1.8); 1.0546 (1.9); 1.0403 (0.9); 0.9410 (0.3); 0.9192 (0.9); 0.8964 (0.4); 0.8464 (0.9); 0.8315 (2.2); 0.8263 (2.2); 0.8146 (2.0); 0.8093 (2.3); 0.7931 (0.7); 0.0480 (0.7); 0.0371 (20.1); 0.0263 (0.8) 21-22: ¹H-NMR(499.9 MHz, d₆-DMSO): δ = 8.7876 (2.3); 8.7708 (2.2); 7.5690 (7.6); 7.2853 (3.7); 7.1907 (3.7); 7.1683 (1.0); 7.1521 (3.0); 7.1440 (2.0); 7.1382 (5.2); 7.1307 (1.7); 7.1272 (1.8); 7.1147 (0.7); 7.1110 (0.5); 7.0821 (3.9); 6.9136 (1.0); 6.9073 (1.1); 6.9005 (1.8); 6.8959 (1.5); 6.8851 (1.0); 6.8820 (0.8); 4.4489 (0.6); 4.4390 (0.8); 4.4314 (1.0); 4.4217 (1.0); 4.4128 (0.7); 4.4033 (0.5); 3.8470 (1.3); 3.8377 (1.4); 3.8248 (2.0); 3.8155 (1.7); 3.7506 (1.8); 3.7381 (1.9); 3.7283 (1.3); 3.7159 (1.2); 3.3402 (33.7); 2.9809 (1.1); 2.9715 (1.2); 2.9533 (1.5); 2.9441 (1.4); 2.8227 (1.5); 2.8037 (1.5); 2.7953 (1.2); 2.7763 (1.0); 2.5890 (19.3); 2.5076 (1.5); 2.5041 (1.9); 2.5008 (1.4); 2.1623 (16.0); 2.0781 (0.5); 2.0678 (0.9); 2.0612 (1.0); 2.0511 (1.6); 2.0409 (1.0); 2.0343 (0.9); 2.0239 (0.4); 1.0292 (1.3); 1.0206 (3.0); 1.0164 (3.2); 1.0083 (1.8); 1.0039 (2.9); 0.9996 (2.9); 0.9916 (1.1); 0.7815 (1.5); 0.7731 (3.4); 0.7697 (3.7); 0.7632 (3.3); 0.7593 (3.3); 0.7505 (1.0) 21-23: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.1287 (0.8); 8.1011 (0.8); 8.0838 (5.4); 7.3700 (2.3); 7.2989 (5.4); 7.2003 (2.2); 7.1917 (0.6); 7.1739 (3.4); 7.1646 (2.7); 7.1595 (2.8); 7.1417 (2.9); 7.1146 (0.7); 6.9988 (1.3); 6.9959 (1.3); 6.9731 (1.0); 6.8947 (0.7); 6.8871 (0.8); 6.8718 (1.1); 6.8621 (0.7); 6.8565 (1.0); 6.8410 (0.5); 4.9293 (0.5); 4.9162 (0.7); 4.9038 (0.7); 4.8915 (0.7); 4.8784 (0.5); 3.9454 (1.0); 3.9314 (1.0); 3.9077 (1.6); 3.8937 (1.5); 3.7643 (1.5); 3.7536 (1.6); 3.7266 (1.1); 3.7158 (1.0); 3.2135 (3.6); 3.1888 (3.6); 2.7288 (16.0); 2.3570 (0.6); 2.3446 (1.0); 2.2942 (11.3); 2.1824 (0.5); 2.1713 (0.5); 2.1542 (1.0); 2.1370 (0.6); 2.1260 (0.6); 1.6160 (1.1); 1.4701 (0.6); 1.2942 (0.6); 1.1013 (0.7); 1.0863 (1.8); 1.0793 (2.0); 1.0648 (1.1); 1.0578 (1.9); 1.0510 (1.8); 1.0366 (0.9); 0.8494 (0.9); 0.8346 (2.2); 0.8293 (2.1); 0.8176 (1.9); 0.8122 (2.3); 0.7958 (0.7); 0.1099 (0.3); 0.0381 (7.4) 21-24: ¹H-NMR(400.1 MHz, CDCl3): δ = 8.1965 (1.1); 8.1766 (1.1); 8.0709 (5.6); 7.2898 (2.9); 7.2617 (11.1); 7.2001 (1.3); 7.1799 (1.7); 7.1760 (1.6); 7.1446 (0.4); 7.1302 (2.8); 7.1249 (3.0); 7.1122 (4.0); 7.0931 (0.4); 7.0663 (2.9); 7.0459 (2.1); 6.8556 (0.8); 6.8489 (0.9); 6.8391 (1.4); 6.8306 (1.2); 6.8155 (0.6); 4.6895 (0.6); 4.6806 (0.8); 4.6715 (0.9); 4.6615 (0.8); 4.6527 (0.6); 3.8142 (1.1); 3.8039 (1.0); 3.7858 (1.6); 3.7754 (1.5); 3.6765 (1.6); 3.6694 (1.6); 3.6481 (1.2); 3.6410 (1.1); 3.0370 (3.8); 3.0182 (4.0); 2.9581 (1.5); 2.8851 (1.4); 2.7112 (16.0); 2.6750 (0.4); 2.6417 (0.3); 2.3943 (13.6); 2.3557 (0.5); 2.3481 (0.4); 2.2663 (0.4); 2.1409 (0.6); 2.1323 (0.7); 2.1199 (1.2); 2.1069 (0.8); 2.0989 (0.7); 2.0855 (0.4); 1.5742 (2.8); 1.0576 (0.8); 1.0461 (2.2); 1.0414 (2.4); 1.0302 (1.4); 1.0249 (2.3); 1.0204 (2.3); 1.0095 (0.9); 0.8054 (1.0); 0.7933 (2.9); 0.7813 (2.6); 0.7778 (2.8); 0.7655 (0.8); −0.0002 (14.8) 21-25: ¹H-NMR(400.1 MHz, CDCl3): δ = 8.2421 (7.0); 8.2130 (1.3); 7.3753 (1.4); 7.3555 (3.1); 7.3357 (1.8); 7.2614 (12.0); 7.0504 (4.7); 7.0311 (5.0); 7.0144 (1.8); 7.0100 (1.9); 6.9944 (1.6); 6.9892 (1.7); 6.9646 (3.6); 6.9255 (3.4); 6.8781 (2.1); 6.8590 (1.6); 4.6679 (0.7); 4.6601 (1.0); 4.6505 (1.1); 4.6409 (1.0); 4.6320 (0.7); 4.6228 (0.4); 3.8142 (1.2); 3.8043 (1.2); 3.7858 (1.9); 3.7760 (1.8); 3.6960 (2.0); 3.6892 (2.0); 3.6676 (1.3); 3.6609 (1.3); 3.0220 (4.8); 3.0033 (4.5); 2.9580 (0.9); 2.8848 (0.8); 2.3626 (16.0); 2.2659 (15.2); 1.9768 (0.4); 1.9641 (0.8); 1.9557 (0.9); 1.9436 (1.6); 1.9312 (1.0); 1.9226 (0.9); 1.9102 (0.4); 1.5745 (20.6); 1.0443 (0.9); 1.0320 (2.8); 1.0279 (2.9); 1.0114 (2.9); 1.0073 (2.7); 0.9959 (1.0); 0.7609 (1.1); 0.7486 (3.6); 0.7332 (3.4); 0.7208 (0.9); −0.0002 (9.2) 21-26: ¹H-NMR(400.1 MHz, CDCl3): δ = 8.2401 (6.7); 8.1113 (1.3); 8.0920 (1.3); 7.2611 (7.1); 7.1552 (0.6); 7.1343 (3.0); 7.1195 (4.5); 7.1100 (1.9); 7.0950 (0.5); 7.0636 (2.5); 7.0445 (3.0); 6.9546 (3.5); 6.8829 (1.2); 6.8722 (3.2); 6.8596 (2.2); 4.6867 (0.4); 4.6771 (0.8); 4.6684 (1.0); 4.6588 (1.1); 4.6496 (1.0); 4.6403 (0.7); 4.6320 (0.4); 3.8215 (1.2); 3.8113 (1.2); 3.7932 (1.9); 3.7830 (1.8); 3.6999 (2.0); 3.6929 (2.0); 3.6716 (1.3); 3.6646 (1.2); 3.0421 (4.9); 3.0235 (4.8); 2.9579 (1.3); 2.8849 (1.3); 2.3683 (16.0); 2.2537 (15.2); 2.1541 (0.4); 2.1415 (0.8); 2.1329 (0.9); 2.1204 (1.5); 2.1079 (0.9); 2.0991 (0.8); 2.0864 (0.4); 1.5844 (10.4); 1.0729 (0.9); 1.0613 (2.7); 1.0567 (2.8); 1.0401 (2.8); 1.0357 (2.6); 1.0247 (1.0); 0.8147 (1.2); 0.8028 (3.5); 0.7903 (3.1); 0.7871 (3.3); 0.7748 (0.9); −0.0002 (5.4) 21-27: ¹H-NMR(400.1 MHz, CDCl3): δ = 8.2684 (6.6); 8.1165 (1.2); 8.0974 (1.2); 8.0164 (0.7); 7.6177 (1.0); 7.5983 (2.4); 7.5786 (1.7); 7.5088 (2.3); 7.4896 (1.5); 7.4046 (3.0); 7.3707 (1.8); 7.3495 (1.5); 7.2620 (12.0); 7.0473 (2.4); 7.0281 (3.0); 6.9631 (3.5); 6.8782 (2.0); 6.8530 (2.1); 6.7114 (2.9); 6.5708 (1.5); 4.6922 (0.4); 4.6823 (0.7); 4.6737 (1.0); 4.6646 (1.0); 4.6545 (1.0); 4.6464 (0.7); 4.6361 (0.4); 3.8304 (1.2); 3.8204 (1.2); 3.8020 (1.9); 3.7920 (1.8); 3.7106 (2.0); 3.7040 (2.0); 3.6824 (1.3); 3.6758 (1.2); 3.0538 (0.4); 3.0327 (3.1); 3.0196 (2.6); 3.0120 (2.5); 2.9758 (0.3); 2.9583 (4.2); 2.8845 (4.0); 2.3613 (16.0); 2.2595 (15.4); 1.5863 (11.1); −0.0002 (9.0) 21-28: ¹H-NMR(400.1 MHz, CDCl3): δ = 8.2539 (6.9); 8.0583 (1.2); 8.0391 (1.2); 7.5067 (1.6); 7.4865 (2.2); 7.4038 (2.4); 7.3991 (3.7); 7.3942 (2.5); 7.3901 (2.2); 7.3694 (3.4); 7.3492 (1.7); 7.2612 (5.9); 7.2017 (1.9); 7.1973 (1.8); 7.1813 (1.5); 7.1771 (1.4); 7.0454 (2.4); 7.0263 (3.0); 6.9676 (3.4); 6.8869 (2.0); 6.8678 (1.6); 4.6826 (0.4); 4.6731 (0.7); 4.6645 (1.0); 4.6549 (1.0); 4.6455 (1.0); 4.6366 (0.7); 4.6267 (0.4); 3.8266 (1.2); 3.8165 (1.2); 3.7982 (1.9); 3.7882 (1.8); 3.7086 (2.0); 3.7019 (2.0); 3.6803 (1.3); 3.6736 (1.2); 3.0306 (3.7); 3.0141 (2.8); 3.0095 (2.8); 2.9573 (1.5); 2.8833 (1.4); 2.3595 (16.0); 2.2715 (15.1); 1.5862 (9.1); −0.0002 (4.4) 21-29: ¹H-NMR(400.1 MHz, CDCl3): δ = 8.2563 (6.9); 8.0676 (1.2); 8.0485 (1.2); 8.0164 (0.6); 7.4493 (1.3); 7.4290 (3.3); 7.4088 (2.3); 7.3538 (2.3); 7.3328 (1.4); 7.2609 (7.1); 7.2515 (2.4); 7.2465 (3.7); 7.2416 (2.1); 7.1557 (1.8); 7.1519 (1.7); 7.1360 (1.6); 7.1315 (1.4); 7.0476 (2.4); 7.0284 (3.0); 6.9665 (3.4); 6.8863 (2.0); 6.8673 (1.6); 4.6842 (0.4); 4.6743 (0.7); 4.6664 (1.0); 4.6569 (1.0); 4.6473 (1.0); 4.6388 (0.7); 4.6285 (0.4); 3.8262 (1.2); 3.8161 (1.2); 3.7978 (1.9); 3.7879 (1.8); 3.7083 (2.1); 3.7016 (2.0); 3.6799 (1.3); 3.6733 (1.2); 3.0508 (0.4); 3.0329 (3.0); 3.0294 (3.1); 3.0162 (2.6); 3.0089 (2.5); 2.9737 (0.3); 2.9576 (3.4); 2.8841 (3.2); 2.3607 (16.0); 2.2697 (15.2); 1.5838 (2.6); −0.0002 (9.2) 21-30: ¹H-NMR(400.1 MHz, CDCl3): δ = 8.2241 (7.2); 8.0182 (3.0); 8.0014 (1.4); 7.6167 (1.0); 7.5969 (2.5); 7.5771 (1.7); 7.5067 (2.3); 7.4875 (1.6); 7.3966 (3.2); 7.3696 (1.9); 7.3496 (1.6); 7.3269 (3.9); 7.2623 (12.4); 7.1392 (2.8); 7.1199 (3.5); 6.9803 (2.2); 6.9619 (1.7); 6.8530 (1.5); 6.7123 (3.1); 6.5716 (1.5); 4.8934 (0.4); 4.8838 (0.7); 4.8745 (1.0); 4.8651 (1.0); 4.8558 (1.0); 4.8470 (0.7); 4.8368 (0.4); 3.9050 (1.4); 3.8948 (1.4); 3.8765 (1.9); 3.8664 (1.8); 3.7293 (1.9); 3.7219 (2.0); 3.7009 (1.5); 3.6935 (1.4); 3.2422 (1.0); 3.2218 (1.0); 3.2073 (1.9); 3.1871 (1.8); 3.1416 (1.8); 3.1246 (1.8); 3.1067 (1.0); 3.0899 (0.9); 2.9579 (12.3); 2.8844 (11.6); 2.2849 (0.7); 2.2625 (16.0); 1.5788 (5.7); −0.0002 (16.0) 21-31: ¹H-NMR(400.1 MHz, CDCl3): δ = 8.1057 (5.5); 7.9851 (1.0); 7.9661 (1.0); 7.6073 (0.8); 7.5867 (1.9); 7.5676 (1.8); 7.5473 (1.0); 7.3795 (1.0); 7.3597 (1.7); 7.3403 (0.7); 7.2614 (20.3); 7.0691 (2.0); 7.0499 (2.4); 6.9502 (2.9); 6.8736 (1.6); 6.8541 (1.3); 4.7029 (0.3); 4.6932 (0.6); 4.6834 (0.8); 4.6745 (0.9); 4.6646 (0.8); 4.6556 (0.6); 3.8291 (1.0); 3.8185 (1.0); 3.8009 (1.6); 3.7905 (1.5); 3.7094 (1.7); 3.7022 (1.7); 3.6811 (1.1); 3.6739 (1.0); 3.0500 (3.9); 3.0313 (3.3); 2.9584 (1.3); 2.8854 (1.2); 2.7219 (16.0); 2.3724 (13.4); 2.2405 (12.6); 1.5600 (8.2); −0.0002 (26.9) 21-32: ¹H-NMR(400.1 MHz, CDCl3): δ = 8.2363 (6.9); 8.1320 (1.2); 8.1122 (1.3); 7.2957 (3.3); 7.2614 (7.9); 7.2051 (1.5); 7.1849 (2.0); 7.1810 (1.8); 7.1625 (0.6); 7.1420 (2.6); 7.1354 (1.9); 7.1259 (4.6); 7.1149 (1.8); 7.0995 (0.5); 7.0945 (0.4); 7.0568 (3.2); 7.0366 (2.5); 6.8876 (0.9); 6.8780 (1.0); 6.8717 (1.5); 6.8652 (1.4); 6.8525 (0.9); 6.8477 (0.8); 4.6903 (0.4); 4.6808 (0.7); 4.6723 (1.0); 4.6626 (1.0); 4.6534 (1.0); 4.6444 (0.7); 4.6351 (0.4); 3.8172 (1.2); 3.8072 (1.2); 3.7888 (1.9); 3.7787 (1.8); 3.6748 (1.9); 3.6679 (1.9); 3.6463 (1.3); 3.6393 (1.3); 3.0370 (4.9); 3.0183 (4.8); 2.9577 (1.4); 2.8846 (1.3); 2.3896 (16.0); 2.1574 (0.3); 2.1440 (0.7); 2.1356 (0.8); 2.1230 (1.4); 2.1103 (0.9); 2.1020 (0.8); 2.0889 (0.4); 1.5655 (4.8); 1.0761 (0.9); 1.0643 (2.6); 1.0598 (2.7); 1.0433 (2.7); 1.0387 (2.6); 1.0277 (1.0); 0.8151 (1.1); 0.8029 (3.4); 0.7907 (3.0); 0.7873 (3.3); 0.7751 (0.9); −0.0002 (10.5) 21-33: ¹H-NMR(400.1 MHz, CDCl3): δ = 8.2021 (7.4); 8.1382 (1.2); 8.1182 (1.2); 8.0192 (1.8); 7.3742 (1.6); 7.3544 (3.4); 7.3348 (5.7); 7.2617 (33.1); 7.1329 (2.8); 7.1135 (3.5); 7.0510 (2.2); 7.0318 (2.0); 7.0076 (1.7); 7.0035 (1.8); 6.9884 (1.5); 6.9832 (1.7); 6.9655 (2.2); 6.9466 (1.8); 6.9186 (3.4); 4.8826 (0.4); 4.8717 (0.7); 4.8637 (1.0); 4.8544 (1.0); 4.8449 (1.0); 4.8350 (0.7); 4.8257 (0.4); 3.8942 (1.4); 3.8840 (1.4); 3.8659 (2.0); 3.8559 (1.8); 3.7141 (1.9); 3.7066 (2.0); 3.6857 (1.5); 3.6783 (1.5); 3.2087 (0.7); 3.1892 (0.7); 3.1742 (2.0); 3.1545 (2.0); 3.1397 (2.0); 3.1222 (2.1); 3.1048 (0.8); 3.0875 (0.6); 2.9587 (12.1); 2.8858 (11.4); 2.2935 (0.5); 2.2687 (16.0); 1.9776 (0.4); 1.9644 (0.8); 1.9561 (1.0); 1.9440 (1.6); 1.9312 (1.0); 1.9228 (0.9); 1.9104 (0.4); 1.5618 (20.4); 1.0463 (0.9); 1.0342 (2.8); 1.0295 (3.0); 1.0133 (3.0); 1.0089 (2.8); 0.9974 (1.1); 0.7615 (1.1); 0.7496 (3.7); 0.7376 (3.1); 0.7334 (3.6); 0.7214 (1.0); −0.0002 (42.6) 21-34: ¹H-NMR(400.1 MHz, CDCl3): δ = 8.2016 (7.2); 8.0188 (2.5); 8.0066 (1.4); 7.3355 (3.8); 7.2623 (9.6); 7.1500 (3.0); 7.1360 (5.2); 7.1307 (4.6); 7.1230 (4.4); 7.1023 (0.6); 6.9693 (2.1); 6.9498 (1.7); 6.8819 (0.9); 6.8693 (1.5); 6.8586 (1.6); 6.8483 (0.9); 6.8416 (0.8); 4.8910 (0.4); 4.8810 (0.7); 4.8722 (1.0); 4.8627 (1.0); 4.8531 (1.0); 4.8441 (0.7); 4.8342 (0.4); 3.9018 (1.4); 3.8916 (1.4); 3.8734 (1.9); 3.8632 (1.8); 3.7233 (1.9); 3.7156 (1.9); 3.6949 (1.5); 3.6871 (1.4); 3.2159 (0.5); 3.1957 (0.5); 3.1813 (2.3); 3.1625 (3.0); 3.1488 (2.3); 3.1314 (0.5); 3.1141 (0.4); 2.9580 (11.4); 2.8848 (10.7); 2.2636 (16.0); 2.1549 (0.3); 2.1412 (0.8); 2.1328 (0.9); 2.1202 (1.5); 2.1075 (1.0); 2.0994 (0.9); 2.0861 (0.4); 1.5849 (3.4); 1.0747 (0.9); 1.0631 (2.7); 1.0586 (2.8); 1.0419 (2.8); 1.0375 (2.7); 1.0264 (1.1); 0.8155 (1.1); 0.8033 (3.4); 0.7912 (3.1); 0.7876 (3.3); 0.7755 (0.9); −0.0002 (12.4) 21-35: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.2404 (0.7); 8.2149 (0.7); 8.1141 (4.5); 7.2986 (8.0); 7.1821 (0.4); 7.1631 (1.9); 7.1555 (2.3); 7.1380 (3.4); 7.1247 (1.9); 7.1121 (0.4); 7.0993 (2.0); 6.8933 (1.6); 6.8865 (1.5); 6.8707 (1.6); 6.8621 (1.6); 6.8401 (0.5); 6.7705 (2.0); 5.3375 (0.7); 4.8836 (0.4); 4.8725 (0.5); 4.8593 (0.6); 4.8463 (0.5); 4.8345 (0.4); 3.8782 (0.7); 3.8642 (0.7); 3.8407 (1.3); 3.8267 (1.2); 3.7612 (1.4); 3.7513 (1.4); 3.7237 (0.8); 3.7138 (0.7); 3.2725 (1.4); 3.2623 (1.6); 3.2499 (1.4); 3.2358 (1.4); 2.7393 (13.4); 2.2968 (0.8); 2.2827 (9.4); 2.1821 (0.5); 2.1709 (0.5); 2.1537 (1.0); 2.1420 (0.8); 2.1353 (0.8); 2.1254 (0.8); 2.1141 (0.9); 2.0965 (0.5); 2.0862 (0.5); 1.6090 (16.0); 1.0992 (0.6); 1.0842 (1.6); 1.0772 (1.8); 1.0624 (1.6); 1.0549 (2.3); 1.0489 (2.7); 1.0340 (1.9); 1.0219 (1.2); 1.0159 (1.5); 1.0045 (0.7); 0.8480 (0.8); 0.8330 (2.0); 0.8279 (1.9); 0.8162 (1.8); 0.8107 (2.0); 0.7944 (0.6); 0.7238 (0.7); 0.7138 (1.5); 0.7076 (1.5); 0.6973 (1.6); 0.6904 (0.9); 0.1076 (2.3); 0.0483 (0.4); 0.0374 (9.5); 0.0266 (0.4)

TABLE 35 Compounds according to formula (22)

Ex No R⁷ R⁸ X

L—R⁶ LogP 22-01 Cl H Cl

(2,4-dimethylphenyl)methyl 3.51^([a]) 22-02 CH₃ H Cl

(2,4-dimethylphenyl)methyl 2.91^([a]) 22-03 Cl H Cl

(4-bromo-2- methylphenyl)methyl 3.66^([a]) 22-04 CH₃ H Cl

(4-bromo-2- methylphenyl)methyl 3.06^([a]) 22-05 Cl H Cl

(2,4-dichlorophenyl)methyl 2.50^([a]) 22-06 CH₃ H Cl

(2,4-dichlorophenyl)methyl 2.06^([a]) In table 35, ″#″ denotes the point of attachment to the L—R⁶ group and ″*″ denotes the point of attachment to the pyridazin-4-yl group.

TABLE 35 22-01: ¹H-NMR(400.1 MHz, CDCl3): δ = 7.7580 (6.8); 7.2614 (12.3); 7.0994 (2.3); 7.0803 (3.1); 7.0260 (3.4); 6.9891 (2.1); 6.9694 (1.5); 6.8424 (1.0); 6.8226 (0.9); 4.6957 (0.4); 4.6842 (0.7); 4.6763 (1.1); 4.6670 (0.9); 4.6564 (1.1); 4.6476 (0.6); 4.6367 (0.4); 3.8240 (1.3); 3.8148 (1.3); 3.7952 (2.0); 3.7862 (1.8); 3.6895 (2.0); 3.6822 (2.0); 3.6607 (1.4); 3.6534 (1.3); 3.0370 (5.0); 3.0178 (4.7); 2.9557 (1.0); 2.8759 (1.0); 2.3856 (16.0); 2.3063 (15.0); 2.2812 (0.4); 1.5601 (11.3); −0.0002 (16.5) 22-02: ¹H-NMR(400.1 MHz, CDCl3): δ = 7.6311 (5.0); 7.2619 (7.1); 7.1157 (1.9); 7.0966 (2.4); 7.0214 (2.7); 6.9844 (1.6); 6.9654 (1.2); 6.9214 (0.8); 6.9012 (0.8); 4.6932 (0.3); 4.6814 (0.5); 4.6735 (0.8); 4.6640 (0.7); 4.6544 (0.8); 4.6465 (0.5); 3.8183 (1.0); 3.8091 (1.0); 3.7896 (1.6); 3.7805 (1.5); 3.6804 (1.6); 3.6731 (1.6); 3.6518 (1.1); 3.6444 (1.1); 3.0375 (3.8); 3.0183 (2.7); 2.7604 (16.0); 2.3922 (12.8); 2.3024 (12.0); 1.5770 (8.4); −0.0002 (9.5) 22-03: ¹H-NMR(400.1 MHz, CDCl3): δ = 8.1668 (0.9); 8.0091 (0.5); 7.8283 (6.5); 7.3646 (3.2); 7.3137 (1.8); 7.2936 (2.1); 7.2620 (27.6); 7.1017 (3.4); 7.0815 (2.7); 6.9418 (1.0); 6.9215 (1.0); 4.6923 (0.4); 4.6714 (1.0); 4.6623 (0.8); 4.6531 (1.0); 4.6338 (0.4); 3.8111 (1.3); 3.8026 (1.3); 3.7820 (1.9); 3.7735 (1.7); 3.6539 (2.0); 3.6468 (1.9); 3.6250 (1.6); 3.6178 (1.6); 3.0516 (0.4); 3.0312 (3.8); 3.0161 (2.6); 3.0091 (2.6); 2.9756 (0.4); 2.9577 (3.2); 2.8802 (2.9); 2.4143 (16.0); 2.3922 (2.2); 1.5604 (20.4); 1.2548 (0.6); −0.0002 (33.4) 22-04: ¹H-NMR(400.1 MHz, CDCl3): δ = 7.6381 (5.1); 7.3565 (2.6); 7.3041 (1.3); 7.2839 (1.6); 7.2797 (1.5); 7.2627 (7.8); 7.1096 (2.6); 7.0893 (2.1); 6.9978 (0.9); 6.9765 (0.8); 4.6988 (0.3); 4.6789 (0.8); 4.6698 (0.7); 4.6604 (0.8); 3.8127 (1.1); 3.8038 (1.1); 3.7838 (1.6); 3.7750 (1.4); 3.6539 (1.6); 3.6469 (1.6); 3.6250 (1.2); 3.6179 (1.1); 3.0328 (3.8); 3.0155 (2.5); 3.0121 (2.5); 2.9556 (0.6); 2.8763 (0.6); 2.7692 (16.0); 2.4174 (13.3); 1.5769 (6.0); −0.0002 (10.2) 22-05: ¹H-NMR(400.1 MHz, CDCl3): δ = 18.7908 (0.3); 16.3068 (0.3); 9.4412 (0.4); 8.0243 (0.3); 8.0119 (1.0); 7.7659 (16.0); 7.5199 (0.6); 7.4619 (0.4); 7.4202 (8.7); 7.4156 (8.3); 7.3272 (0.5); 7.3005 (5.3); 7.2798 (11.9); 7.2618 (113.7); 7.2453 (6.8); 7.2406 (5.9); 7.2247 (3.0); 7.2198 (2.6); 7.1244 (0.4); 6.9987 (0.9); 6.9608 (2.2); 6.9437 (2.2); 6.8868 (0.4); 4.5419 (0.8); 4.5325 (1.1); 4.5225 (1.6); 4.5136 (2.8); 4.5036 (2.4); 4.4936 (2.6); 4.4856 (1.7); 4.4744 (1.2); 4.4673 (0.6); 3.8436 (1.8); 3.8179 (3.5); 3.7669 (3.7); 3.7607 (3.6); 3.7400 (2.0); 3.7336 (1.7); 3.7117 (0.4); 3.5758 (0.4); 3.5509 (0.4); 3.5296 (0.4); 3.5157 (0.4); 3.2221 (0.3); 3.1851 (0.5); 3.1484 (8.7); 3.1295 (8.5); 3.0928 (0.4); 2.9586 (5.4); 2.9111 (0.4); 2.8814 (5.1); 1.9549 (0.7); 1.9279 (2.4); 1.7447 (0.4); 1.6874 (0.4); 1.6781 (0.4); 1.5566 (103.3); 1.4813 (0.4); 1.3480 (0.4); 1.2869 (0.4); 1.2564 (0.9); 1.2369 (0.4); 0.8855 (0.4); 0.8455 (0.4); 0.1459 (0.8); −0.0002 (147.4); −0.1491 (0.7); −3.4400 (0.4) 22-06: ¹H-NMR(400.1 MHz, CDCl3): δ = 7.5766 (5.2); 7.4137 (3.0); 7.4088 (2.9); 7.3099 (1.9); 7.2894 (3.3); 7.2619 (38.8); 7.2370 (2.1); 7.2322 (1.9); 7.2165 (1.1); 7.2116 (1.1); 6.9980 (0.4); 6.9818 (0.8); 6.9619 (0.8); 4.5338 (0.4); 4.5240 (0.6); 4.5143 (1.0); 4.5039 (0.8); 4.4945 (0.9); 4.4859 (0.6); 4.4746 (0.4); 3.8543 (0.6); 3.8283 (1.1); 3.7658 (1.1); 3.7338 (0.6); 3.1495 (4.1); 3.1305 (3.9); 2.9584 (1.6); 2.8825 (1.5); 2.7561 (16.0); 2.7243 (1.1); 2.1569 (0.8); 1.5602 (30.8); 1.2889 (0.5); 1.2726 (0.5); 1.1257 (0.4); 1.1093 (0.4); −0.0002 (50.5)

TABLE 37 Compounds according to formula (23)

Ex No R⁷ R⁸ X

L—R⁶ LogP 23-01 Cl H Cl

(2,4-dimethylphenyl)methyl 3.40^([a]) 23-02 Cl H Cl

(4-bromo-2- methylphenyl)methyl 3.54^([a]) 23-03 CH₃ H Cl

(4-bromo-2- methylphenyl)methyl 2.98^([a]) 23-04 Cl H Cl

(2,4-dichlorophenyl)methyl 3.54^([a]) 23-05 CH₃ H Cl

(2,4-dichlorophenyl)methyl 2.95^([a]) In table 37, ″#″ denotes the point of attachment to the L—R⁶ group and ″*″ denotes the point of attachment to the pyridazin-4-yl group.

TABLE 38 23-05: ¹H-NMR(400.1 MHz, CDCl3): δ = 7.6204 (0.4); 7.4786 (0.3); 7.4252 (0.8); 7.3994 (0.6); 7.3891 (0.6); 7.3660 (0.5); 7.3395 (0.7); 7.3170 (1.1); 7.2981 (4.5); 7.2937 (5.0); 7.2618 (35.2); 7.2446 (3.6); 7.2282 (1.0); 7.1930 (4.7); 7.1726 (3.0); 7.1594 (1.6); 7.1347 (0.9); 7.1108 (0.9); 7.0865 (2.1); 7.0495 (0.4); 6.9975 (0.8); 6.4099 (1.0); 5.7768 (1.4); 5.7485 (1.4); 5.3015 (1.8); 4.8146 (0.9); 3.9885 (1.3); 3.9436 (1.4); 3.8619 (1.1); 3.8519 (1.1); 3.8327 (1.3); 3.8249 (1.4); 3.7953 (0.4); 3.7766 (0.3); 3.7351 (0.3); 3.7169 (0.4); 3.6961 (0.5); 3.6750 (1.6); 3.6682 (1.6); 3.6468 (1.3); 3.6399 (1.2); 3.4547 (1.2); 3.4257 (0.7); 3.4152 (0.4); 3.1434 (0.4); 3.1253 (0.4); 3.0425 (1.3); 3.0294 (1.3); 3.0075 (2.0); 2.9956 (1.7); 2.9346 (1.8); 2.9120 (1.6); 2.9008 (1.1); 2.8785 (0.9); 2.7647 (1.2); 2.7527 (0.4); 2.7387 (0.5); 2.7243 (0.8); 2.6389 (16.0); 2.3125 (2.6); 2.2921 (0.5); 2.2428 (2.5); 2.2073 (0.4); 2.1827 (0.4); 2.1544 (0.4); 2.1352 (0.4); 2.0808 (0.5); 1.9494 (0.4); 1.9100 (0.5); 1.8657 (0.6); 1.8472 (0.6); 1.8433 (0.6); 1.6803 (1.4); 1.6586 (1.5); 1.6427 (1.5); 1.5923 (1.6); 1.5746 (1.9); 1.5584 (2.0); 1.5424 (1.8); 1.4477 (1.0); 1.4293 (1.0); 1.3756 (0.8); 1.2541 (8.4); 1.2070 (1.5); 1.1365 (0.8); 1.1258 (0.8); 1.1101 (0.8); 1.0896 (0.6); 1.0386 (0.5); 1.0184 (0.5); 1.0044 (0.5); 0.9810 (0.5); 0.8797 (1.8); 0.8582 (2.9); 0.8425 (3.0); −0.0002 (37.0)

TABLE 39 Compounds according to formula (25)

Ex No R⁷ R⁸ Q Y LogP 25-01 Cl H 3-cyclopropylphenyl CH₃ 3.08^([a]) 25-02 Cl H 3-(trifluoromethyl)phenyl CH₃ 3.00^([a])

TABLE 40 25-02: ¹H-NMR(300.2 MHz, CDCl3): δ = 8.3217 (0.8); 8.2067 (0.3); 7.9791 (1.3); 7.9518 (5.6); 7.9445 (3.3); 7.8565 (0.4); 7.8352 (4.0); 7.8335 (4.2); 7.8211 (1.1); 7.7997 (0.6); 7.6983 (0.8); 7.6463 (0.8); 7.6264 (3.1); 7.6051 (6.6); 7.5701 (2.2); 7.5341 (4.0); 7.4973 (0.7); 7.4804 (1.8); 7.4711 (2.6); 7.4637 (2.5); 7.4507 (1.9); 7.3467 (1.2); 7.3206 (2.6); 7.2997 (4.1); 7.1607 (2.8); 7.1326 (4.4); 7.0469 (1.8); 7.0194 (1.6); 4.5171 (0.5); 4.4932 (0.4); 4.4743 (0.6); 4.4604 (0.4); 4.4508 (2.0); 4.4367 (0.5); 4.4271 (2.0); 4.4127 (0.7); 4.4036 (0.8); 4.3890 (1.7); 4.3653 (1.4); 4.3435 (1.0); 4.3167 (10.9); 4.3132 (9.9); 4.2989 (3.0); 4.2520 (3.8); 4.2483 (3.6); 4.2031 (0.3); 4.1751 (0.5); 4.0500 (3.8); 4.0223 (16.0); 4.0078 (1.7); 3.9919 (3.4); 3.9624 (10.8); 2.0707 (1.2); 1.5051 (1.8); 1.4812 (4.3); 1.4655 (1.7); 1.4570 (3.6); 1.4422 (3.2); 1.4333 (2.0); 1.4185 (1.8); 1.4101 (1.0); 1.2849 (0.4); 1.2739 (0.4); 0.0297 (3.2)

TABLE 41 Compounds according to formula (30)

Ex No R⁷ R⁸ Q

R⁶ LogP 30-01 CH₃ H 3-(trifluoro- methyl)phenyl

1-methyl-1H- indol-5-yl 3.92^([a]) In table 41, ″#″ denotes the point of attachment to the R⁶ group and ″*″ denotes the point of attachment to the pyridazin-4-yl group.

TABLE 42 30-01: ¹H-NMR(400.1 MHz, d₆-DMSO): δ = 7.9615 (2.0); 7.7306 (6.3); 7.7206 (3.1); 7.6923 (2.0); 7.6727 (1.9); 7.6479 (2.4); 7.6283 (1.3); 7.5904 (1.7); 7.5736 (4.3); 7.4225 (0.4); 7.4047 (1.5); 7.3833 (2.8); 7.3375 (2.3); 7.3157 (4.2); 7.3081 (3.3); 6.7820 (1.5); 6.7422 (1.9); 6.4213 (3.9); 6.4019 (3.6); 6.3940 (3.2); 6.3874 (1.9); 6.3715 (0.8); 6.3636 (0.8); 6.3475 (1.2); 6.3319 (0.6); 4.6461 (3.1); 4.6307 (3.1); 3.7957 (1.3); 3.7839 (16.0); 3.7691 (1.4); 3.3382 (32.0); 2.8983 (11.7); 2.7392 (10.7); 2.5978 (1.3); 2.5873 (14.6); 2.5735 (1.6); 2.5143 (10.9); 2.5102 (14.5); 2.5061 (11.3)

Biological Data

The advanced fungicidal activity of the active compound combinations according to the invention is evident from the example below. While the individual active compounds exhibit weaknesses with regard to the fungicidal activity, the combinations have an activity, which exceeds a simple addition of activities.

A synergistic effect of fungicides is always present, when the fungicidal activity of the active compound combinations exceeds the total of activities of the active compounds when applied individually. The expected activity for a given combination of two active compounds can be calculated as follows (cf. Colby, S. R., “Calculating Synergistic and Antagonistic Responses of Herbicide Combinations”, Weeds 1967, 15, 20-22):

If

-   X is the efficacy when active compound A is applied at an     application rate of m ppm (or g/ha), -   Y is the efficacy when active compound B is applied at an     application rate of n ppm (or g/ha), -   E is the efficacy when the active compounds A and B are applied at     application rates of m and n ppm (or g/ha), respectively, and     then

$E = {X + Y - \frac{X \cdot Y}{100}}$

The degree of efficacy expressed in % is denoted: 0% means an efficacy, which corresponds to that of the control, while an efficacy of 100% means that no disease is observed.

If the actual fungicidal activity exceeds the calculated value, then the activity of the combination is super-additive, i.e. a synergistic effect exists. In this case, the efficacy, which was actually observed, must be greater than the value for the expected efficacy (E), that was calculated from the abovementioned formula.

A further way of demonstrating a synergistic effect is the method of Tammes (cf. “Isoboles, a graphic representation of synergism in pesticides” in Neth. J. Plant Path., 1964, 70, 73-80).

The invention is illustrated by the following examples. However, the invention is not limited to the examples.

Example: In Vitro-Test with Fungal Microorganisms

Method A

Wells of 96-well microtiter plates are filled with 10 μl of a preparation of test compound or compound combination in methanol+emulsifier alkylaryl-polyglycol-ether. Thereafter, the solvent is evaporated in a hood. At the next step, 100 μl of liquid potato dextrose medium is given into each well, that has been amended with an appropriate concentration of spores or mycelium suspension of the test fungus.

With the aid of a photometer, the extinction in all wells is measured at the wavelength of 620 nm.

The microtiter plates are incubated at 20° C. and 85% relative humidity. The inhibition of growth is determined again photometrically 3-5 days after the application. Efficacy is calculated in relation to the untreated control, 0% efficacy means fungal growth as high as in untreated control while 100% efficacy means no fungal growth is measured.

Method B

Wells of 96-well microtiter plates are filled with 30 μl of a preparation of test compound or compound combination in methanol+emulsifier alkylaryl-polyglycol-ether. Thereafter, the solvent is evaporated in a hood. At the next step, 200 μl of liquid growth medium is given, that has been amended with an appropriate concentration of spores or mycelium suspension of the test fungus.

With the aid of a photometer, the extinction in all wells is measured at the wavelength of 600 nm.

The microtiter plates are incubated for 3 to 7 days at 20° C. and 85% relative humidity. After the incubation inhibition of growth is determined photometrically. Efficacy is calculated in relation to the untreated control, 0% efficacy means fungal growth as high as in untreated control while 100% efficacy means no fungal growth is measured.

The data in tables A1 to A12, B1 to B14, C1 to C10, D1 to D8, E1 to E8, F1 to F11, G1 to G4, H1 to H4 and I1 to I5 were collected according to Method A. The data in tables A13 to A22, B15 to B18, C11 to C20, E9 to E16, F12 to F15, G5 to G15, H5 to H8, I6 to I11 and J1 to J11 were collected according to Method B.

TABLE A1 in vitro -Test with Alternaria alternate (7.005) (2.005) (2.028) pyri- (2.002) fluo- inpyr- Effi- Colby (I-052) methanil bixafen pyram fluxam cacy expected (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 72 0.02 9 0.004 0 0.0008 2 20 82 4 93 0.8 0 0.16 0 1.0 46 0.2 66 0.04 23 0.008 29 20.0 82 4.0 63 0.8 57 0.16 17 1.0 80 0.2 22 0.04 10 0.008 0 0.1 20 1:200 99 95 0.1 4 1:40 99 98 0.1 0.8 1:8 91 72 0.1 0.16 1:1.6 100 72 0.1 1.0 1:10 100 85 0.1 0.2 1:2 99 91 0.1 0.04 1:0.4 99 79 0.1 0.008 1:0.08 100 80 0.1 20.0 1:200 100 95 0.1 4.0 1:40 99 90 0.1 0.8 1:8 100 88 0.1 0.16 1:1.6 100 77 0.1 1.0 1:10 99 95 0.1 0.2 1:2 100 78 0.1 0.04 1:0.4 99 75 0.1 0.008 1:0.08 100 72

TABLE A2 in vitro -Test with Alternaria alternate (2.038) (3.025) (3.020) (1.002) isoflucy- fenpi- trifloxy- difeno- Effi- Colby (I-052) pram coxamid strobin conazole cacy expected (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 72 0.02 9 0.004 0 0.0008 2 1.0 82 0.2 77 0.04 70 0.008 43 5.0 76 1.0 41 0.2 2 0.04 5 1.0 96 0.2 95 0.04 87 0.008 44 1.0 96 0.2 28 0.04 10 0.008 27 0.02 1.0 1:50 95 82 0.02 0.2 1:10 96 77 0.02 0.04 1:2 73 70 0.02 0.008 1:0.4 70 43 0.02 5.0 1:250 79 76 0.02 1.0 1:50 54 41 0.02 0.2 1:10 38 2 0.02 0.04 1:2 25 5 0.02 1.0 1:50 99 96 0.02 0.2 1:10 97 95 0.02 0.04 1:2 95 87 0.02 0.008 1:0.4 68 44 0.004 1.0 1:250 93 96 0.004 0.2 1:50 58 28 0.004 0.04 1:10 22 10 0.004 0.008 1:2 13 27

TABLE A3 in vitro -Test with Alternaria alternate (5.012) (5.018) Colby (I-052) folpet propineb Efficacy expected (ppm) (ppm) (ppm) Ratio % value % 0.1 72 0.02 9 0.004 0 0.0008 2 10.0 100 2.0 100 0.4 20 0.08 4 100.0 98 20.0 69 4.0 15 0.8 15 0.02 10.0 1:500 100 100 0.02 2.0 1:100 100 100 0.02 0.4 1:20 53 30 0.02 0.08 1:4 47 16 0.02 100.0 1:5000 95 99 0.02 20.0 1:1000 86 79 0.02 4.0 1:200 75 41 0.02 0.8 1:40 39 41

TABLE A4 in vitro -Test with Alternaria alternate (7.005) (2.005) (2.038) pyri- fluo- isoflu- Colby (I-300) methanil pyram cypram Efficacy expected (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 100 0.02 48 0.004 19 0.0008 7 20.0 100 4.0 100 0.8 100 0.16 43 20.0 99 4.0 80 0.8 86 0.16 76 1.0 84 0.2 85 0.04 71 0.008 52 0.02 20.0 1:1000 100 100 0.02 4.0 1:200 100 100 0.02 0.8 1:40 100 100 0.02 0.16 1:8 97 71 0.0008 20.0 1:25000 100 100 0.0008 4.0 1:5000 99 100 0.0008 0.8 1:1000 100 100 0.0008 0.16 1:200 84 47 0.0008 20.0 1:25000 94 99 0.0008 4.0 1:5000 86 82 0.0008 0.8 1:1000 91 87 0.0008 0.16 1:200 81 78 0.02 1.0 1:50 87 84 0.02 0.2 1:10 86 85 0.02 0.04 1:2 76 71 0.02 0.008 1:0.4 57 52

TABLE A5 in vitro -Test with Alternaria alternate (3.020) (1.002) (1.055) (1.018) trifloxy- difeno- mefentriflu- prothio- Colby (I-300) strobin conazole conazole conazole Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 100 0.02 0 0.004 1 0.0008 20 1.0 99 0.2 97 0.04 78 0.008 51 1.0 91 0.2 39 0.04 17 0.008 2 1.0 100 0.2 96 0.04 58 0.008 9 1.0 100 0.2 94 0.04 15 0.008 20 0.02 1.0 1:50 98 99 0.02 0.2 1:10 97 97 0.02 0.04 1:2 91 78 0.02 0.008 1:0.4 66 51 0.02 1.0 1:50 96 91 0.02 0.2 1:10 49 39 0.02 0.04 1:2 21 17 0.02 0.008 1:0.4 9 2 0.02 1.0 1:50 100 100 0.02 0.2 1:10 100 96 0.02 0.04 1:2 95 59 0.02 0.008 1:0.4 8 11 0.02 1.0 1:50 100 100 0.02 0.2 1:10 100 94 0.02 0.04 1:2 27 17 0.02 0.008 1:0.4 52 22

TABLE A6 in vitro -Test with Alternaria alternate (1.020) (13.001) (13.004) spirox- fludi- proqui- Colby (I-300) amine (15.064) oxonil nazid Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 84 0.02 0 0.004 2 0.0008 0 20.0 16 4.0 12 0.8 18 0.16 0 10.0 50 2.0 12 0.4 5 0.08 2 5.0 100 1.0 97 0.2 17 0.04 9 10.0 9 2.0 0 0.4 6 0.08 19 0.1 20.0 1:200 98 87 0.1 4.0 1:40 100 86 0.1 0.8 1:8 100 87 0.1 0.16 1:1.6 99 84 0.1 10.0 1:200 87 50 0.1 2.0 1:40 16 12 0.1 0.4 1:8 7 5 0.1 0.08 1:1.6 9 2 0.1 5.0 1:50 100 100 0.1 1.0 1:10 100 100 0.1 0.2 1:2 98 87 0.1 0.04 1:0.4 97 85 0.1 10.0 1:100 100 85 0.1 2.0 1:20 100 84 0.1 0.4 1:4 100 85 0.1 0.08 1:0.8 100 87

TABLE A7 in vitro -Test with Alternaria alternate (15.016) (5.003) (5.012) metra- Colby (I-300) captan folpet fenone Efficacy expected (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 100 0.02 2 0.004 0 0.0008 0 20.0 56 4.0 46 0.8 0 0.16 4 10.0 100 2.0 100 0.4 7 0.08 0 20.0 11 4.0 0 0.8 0 0.16 0 0.02 20.0 1:200 100 57 0.02 4.0 1:40 86 47 0.02 0.8 1:8 7 2 0.02 0.16 1:1.6 6 6 0.0008 20.0 1:25000 95 56 0.0008 4.0 1:5000 78 46 0.0008 0.8 1:1000 19 0 0.0008 0.16 1:200 0 4 0.02 10.0 1:500 100 100 0.02 2.0 1:100 100 100 0.02 0.4 1:20 31 9 0.02 0.08 1:4 21 2 0.0008 10.0 1:12500 100 100 0.0008 2.0 1:2500 100 100 0.0008 0.4 1:500 8 7 0.0008 0.08 1:100 0 0 0.004 20.0 1:5000 51 11 0.004 4.0 1:1000 14 0 0.004 0.8 1:200 10 0 0.004 0.16 1:40 0 0

TABLE A8 in vitro -Test with Alternaria alternate (1.020) (13.001) (13.004) spirox- fludi- proqui- Effi- Colby (I-300) amine (15.064) oxonil nazid cacy expected (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 84 0.02 0 0.004 2 0.0008 0 20.0 16 4.0 12 0.8 18 0.16 0 10.0 50 2.0 12 0.4 5 0.08 2 5.0 100 1.0 97 0.2 17 0.04 9 10.0 9 2.0 0 0.4 6 0.08 19 0.1 20.0 1:200 98 87 0.1 4.0 1:40 100 86 0.1 0.8 1:8 100 87 0.1 0.16 1:1.6 99 84 0.1 10.0 1:200 87 50 0.1 2.0 1:40 16 12 0.1 0.4 1:8 7 5 0.1 0.08 1:1.6 9 2 0.1 5.0 1:50 100 100 0.1 1.0 1:10 100 100 0.1 0.2 1:2 98 87 0.1 0.04 1:0.4 97 85 0.1 10.0 1:100 100 85 0.1 2.0 1:20 100 84 0.1 0.4 1:4 100 85 0.1 0.08 1:0.8 100 87

TABLE A9 in vitro -Test with Alternaria alternate (5.012) (15.016) Colby (I-300) folpet metrafenone Efficacy expected (ppm) (ppm) (ppm) Ratio % value % 0.1 84 0.02 0 0.004 2 0.0008 0 10.0 100 2.0 100 0.4 7 0.08 0 20.0 11 4.0 0 0.8 0 0.16 0 0.02 10.0 1:500 100 100 0.02 2.0 1:100 100 100 0.02 0.4 1:20 31 9 0.02 0.08 1:4 21 2 0.004 10.0 1:12500 100 100 0.004 2.0 1:2500 100 100 0.004 0.4 1:500 8 7 0.004 0.08 1:100 0 0 0.004 20.0 1:5000 51 11 0.004 4.0 1:1000 14 0 0.004 0.8 1:200 10 0 0.004 0.16 1:40 0 0

TABLE A10 in vitro -Test with Alternaria alternate (7.005) (2.028) (2.038) pyrime- inpyr- isoflu- Colby (I-302) thanil fluxam cypram Efficacy expected (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 100 0.02 36 0.004 6 0.0008 9 20.0 100 4.0 100 0.8 100 0.16 58 1.0 80 0.2 67 0.04 62 0.008 0 0.2 83 0.04 74 0.008 43 0.02 20.0 1:1000 100 100 0.02 4.0 1:200 100 100 0.02 0.8 1:40 100 100 0.02 0.16 1:8 100 94 0.0008 20.0 1:25000 100 100 0.0008 4.0 1:5000 100 100 0.0008 0.8 1:1000 100 100 0.0008 0.16 1:200 93 58 0.0008 1.0 1:1250 84 80 0.0008 0.2 1:250 71 67 0.0008 0.04 1:50 67 62 0.0008 0.008 1:10 14 0 0.1 0.2 1:2 100 100 0.1 0.04 1:0.4 100 100 0.1 0.008 1:0.08 100 100 0.02 0.2 1:10 88 85 0.02 0.04 1:2 79 78 0.02 0.008 1:0.4 71 51 0.004 0.2 1:50 89 83 0.004 0.04 1:10 72 74 0.004 0.008 1:2 68 43 0.0008 0.2 1:250 93 86 0.0008 0.04 1:50 79 80 0.0008 0.008 1:10 60 55

TABLE A11 in vitro -Test with Alternaria alternate (3.025) (3.020) (1.055) mefen- Colby (I-302) fenpicoxamid trifloxystrobin trifluconazole Efficacy expected (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 100 0.02 36 0.004 6 0.0008 9 5.0 59 1.0 30 0.2 7 0.04 9 1.0 96 0.2 98 0.04 79 0.008 58 1.0 99 0.2 100 0.04 32 0.02 5.0 1:250 71 65 0.02 1.0 1:50 55 40 0.02 0.2 1:10 39 20 0.02 0.04 1:2 31 22 0.02 1.0 1:50 100 97 0.02 0.2 1:10 93 98 0.02 0.04 1:2 86 82 0.02 0.008 1:0.4 83 64 0.004 1.0 1:250 99 96 0.004 0.2 1:50 96 98 0.004 0.04 1:10 80 79 0.004 0.008 1:2 68 58 0.02 1.0 1:50 100 99 0.02 0.2 1:10 100 100 0.02 0.04 1:2 48 35 0.004 1.0 1:250 100 99 0.004 0.2 1:50 100 100 0.004 0.04 1:10 68 36 0.0008 1.0 1:1250 100 99 0.0008 0.2 1:250 100 100 0.0008 0.04 1:50 55 32

TABLE A12 in vitro-Test with Alternaria alternate (5.018) (A1.5) (1.021) (1.020) (13.001) (5.003) pro- Paenibacillus Colby (I-302) tebuconazole spiroxamine fludioxonil captan pineb terrae Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 100 0.02 36 0.004 6 0.0008 9 1.0 98 0.2 26 0.04 19 0.008 13 20.0 22 4.0 21 0.8 20 0.16 3 5.0 100 1.0 98 0.2 18 0.04 0 4.0 100 0.8 20 0.16 0 20.0 97 4.0 72 0.8 19 200.0 81 40.0 0 8.0 0 1.6 0 0.02 1.0 1:50 99 98 0.02 0.2 1:10 70 29 0.02 0.04 1:2 27 23 0.02 0.008 1:0.4 20 17 0.02 20.0 1:1000 30 22 0.02 4.0 1:200 38 21 0.02 0.8 1:40 48 20 0.02 0.16 1:8 28 3 0.02 5.0 1:250 100 100 0.02 1.0 1:50 98 98 0.02 0.2 1:10 56 18 0.02 0.04 1:2 34 0 0.004 4.0 1:1000 100 100 0.004 0.8 1:200 44 21 0.004 0.16 1:40 13 2 0.004 20.0 1:5000 98 98 0.004 4.0 1:1000 79 73 0.004 0.8 1:200 25 24 0.02 200.0 1:10000 100 90 0.02 40.0 1:2000 53 49 0.02 8.0 1:400 48 49 0.02 1.6 1:80 61 49 0.004 200.0 1:50000 97 83 0.004 40.0 1:10000 0 9 0.004 8.0 1:2000 27 9 0.004 1.6 1:400 18 9 0.0008 200.0 1:250000 94 81 0.0008 40.0 1:50000 5 0 0.0008 8.0 1:10000 0 0 0.0008 1.6 1:2000 0 0

TABLE A13 in vitro-Test with Alternaria alternata (2.002) (5.003) (1.002) (5.010) (3.025) Colby (I-339) (17.001) bixafen captan difenoconazole dithianon fenpicoxamid Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 100 0.2 100 0.04 100 0.008 9 8 8 1.6 0 1 59 0.008 13 5 79 1 14 1 94 0.4 0 1 61 0.04 14 0.008 6 0.2 8 1:40 100 100 0.2 1.6 1:8 100 100 0.008 8 1:1000 34 17 0.008 1.6 1:200 16 9 1 1 1:1 100 100 1 0.008 1:0.008 100 100 0.04 1 1:25 100 100 0.04 0.008 1:0.2 100 100 0.008 1 1:125 100 63 0.008 0.008 1:1 35 21 0.04 5 1:125 100 100 0.04 1 1:25 100 100 0.008 5 1:625 100 81 0.008 1 1:125 21 22 0.2 1 1:5 100 100 0.04 1 1:25 99 100 0.008 1 1:125 99 95 0.2 0.4 1:2 100 100 0.04 0.4 1:10 100 100 0.008 0.4 1:50 48 22 0.2 1 1:5 100 100 0.2 0.04 1:0.2 100 100 0.2 0.008 1:0.04 100 100 0.008 1 1:125 77 70 0.008 0.04 1:5 43 34 0.008 0.008 1:1 47 27

TABLE A14 in vitro-Test with Alternaria alternata (2.038) (1.055) (13.001) (15.043) (5.012) isoflucy- (6.002) mefentri- Colby (I-339) fludioxonil fluoxapiprolin folpet pram isotianil fluconazole Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 100 0.2 100 0.04 100 0.008 44 5 99 0.2 18 0.04 13 0.8 0 0.16 0 0.2 7 0.04 3 0.008 6 0.008 22 4 0 0.8 0 1 99 0.2 65 0.2 5 1:25 100 100 0.2 0.2 1:1 100 100 0.2 0.04 1:0.2 100 100 0.008 5 1:625 100 100 0.008 0.2 1:25 45 36 0.008 0.04 1:5 48 32 0.04 0.8 1:20 100 100 0.04 0.16 1:4 100 100 0.008 0.8 1:100 49 49 0.008 0.16 1:20 61 49 0.008 0.2 1:25 56 49 0.008 0.04 1:5 52 47 0.008 0.008 1:1 50 48 0.2 0.008 1:0.04 100 100 0.04 0.008 1:0.2 99 100 0.008 0.008 1:1 66 57 0.04 4 1:100 100 100 0.04 0.8 1:20 99 100 0.008 4 1:500 50 44 0.008 0.8 1:100 47 44 0.2 1 1:5 100 100 0.2 0.2 1:1 100 100 0.008 1 1:125 98 99 0.008 0.2 1:25 95 81

TABLE A15 in vitro-Test with Alternaria alternata (17.012) (13.004) (1.018) (15.016) Paenibacillus (5.018) pro- prothio- (7.005) Colby (I-339) metrafenone terrae propineb quinazid conazole pyrimethanil Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 100 0.2 100 0.04 100 0.008 0 1 0 200.0 100 40.0 4 8 0 1.6 0 100.0 97 20.0 50 4 10 0.8 10 10.0 5 2.0 0 0.4 10 0.08 11 0.5 99 0.1 100 0.02 89 0.004 46 20.0 100 0.8 96 0.16 0 1 1 1:1 100 100 0.2 1 1:5 100 100 0.008 1 1:125 93 86 0.008 200.0 1:25000 100 100 0.008 40.0 1:5000 94 86 0.008 8 1:1000 98 86 0.008 1.6 1:200 97 86 0.008 100.0 1:12500 98 98 0.008 20.0 1:2500 71 56 0.008 4 1:500 85 20 0.008 0.8 1:100 90 20 0.008 10.0 1:1250 75 16 0.008 2.0 1:250 63 12 0.008 0.4 1:50 67 21 0.008 0.08 1:10 68 21 0.008 0.5 1:62.5 99 99 0.008 0.1 1:12.5 99 100 0.008 0.02 1:2.5 99 90 0.008 0.004 1:0.5 98 52 0.008 20.0 1:2500 99 100 0.008 0.8 1:100 99 97 0.008 0.16 1:20 98 12

TABLE A16 in vitro-Test with Alternaria alternata (13.005) (1.020) (2.002) (5.003) Colby (I-339) quinoxyfen spiroxamin (I-338) bixafen captan Efficacy expected (ppm) (ppm) (ppm) (ppm) (1.067) (ppm) (ppm) Ratio % value % 1 100 0.2 100 0.04 100 0.008 79 10 30 20 15 4 15 0.8 3 0.16 0 1 22 0.2 8 0.04 0 0.008 1 0.016 0 1 85 0.04 67 0.008 23 5 100 1 58 0.2 0 1 10 1:10 100 100 0.2 10 1:50 100 100 0.008 10 1:1250 90 85 0.008 20 1:2500 83 82 0.008 4 1:500 82 82 0.008 0.8 1:100 87 79 0.008 0.16 1:20 86 79 1 0.016 1:0.016 49 22 0.2 0.016 1:0.08 10 8 0.04 0.016 1:0.4 0 0 0.04 1 1:25 85 85 0.04 0.04 1:1 75 67 0.04 0.008 1:0.2 32 23 1 5 1:5 100 100 1 1 1:1 100 68 1 0.2 1:0.2 63 22

TABLE A17 in vitro-Test with Alternaria alternata (1.002) difeno- (5.010) (13.001) (2.005) (15.043) (3.012) Colby (I-338) conazole dithianon fludioxonil fluopyram fluoxapiprolin fluoxastrobin Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 68 0.2 0 0.04 2 0.008 3 1 100 0.2 53 0.04 21 2 32 0.2 28 20 91 4 81 0.8 79 0.16 59 0.8 0 0.4 70 1 1 1:5 99 100 1 0.2 1:1 56 53 1 0.04 1:0.2 44 21 1 2 1:2 84 78 0.2 2 1:10 43 32 0.008 2 1:250 45 34 0.2 0.2 1:1 57 28 0.04 0.2 1:5 32 29 0.008 0.2 1:25 59 30 0.2 20 1:100 95 91 0.2 4 1:20 94 81 0.2 0.8 1:4 77 79 0.2 0.16 1:0.8 68 59 0.04 4 1:100 89 82 0.04 0.8 1:20 82 80 0.04 0.16 1:4 63 60 0.008 4 1:500 94 81 0.008 0.8 1:100 74 79 0.008 0.16 1:20 65 59 1 0.8 1:0.8 43 38 0.2 0.8 1:4 17 0 0.04 0.8 1:20 3 3 0.008 0.8 1:100 0 0 0.2 0.4 1:2 68 70 0.04 0.4 1:10 80 71 0.008 0.4 1:50 91 70

TABLE A18 in vitro-Test with Alternaria alternata (1.062) (5.012) (15.012) (2.028) (2.038) (6.002) Colby (I-338) fluoxytioconazole folpet fosetylal inpyrfluxam isoflucypram isotianil Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 38 0.2 0 0.04 3 0.008 0 0.008 5 1 83 4 2 0.8 0 1 75 0.2 50 0.04 9 1 77 20 11 4 15 1 0.008 1:0.008 69 41 0.04 0.008 1:0.2 14 8 0.008 0.008 1:1 9 5 1 1 1:1 100 89 0.04 1 1:25 90 83 0.008 1 1:125 98 83 1 4 1:4 41 36 1 0.8 1:0.8 38 35 0.2 4 1:20 25 2 0.2 0.8 1:4 8 0 0.04 4 1:100 15 2 0.04 0.8 1:20 0 0 1 1 1:1 85 84 1 0.2 1:0.2 76 68 1 0.04 1:0.04 61 41 0.2 1 1:5 76 75 0.2 0.2 1:1 52 50 0.2 0.04 1:0.2 24 9 0.04 1 1:25 84 75 0.04 0.2 1:5 52 50 0.04 0.04 1:1 15 9 0.008 1 1:125 80 75 0.008 0.2 1:25 69 50 0.008 0.04 1:5 8 9 1 1 1:1 95 85 0.2 1 1:5 90 77 0.04 1 1:25 80 77 0.008 1 1:125 87 77 1 20 1:20 44 35 1 4 1:4 38 32 0.2 20 1:100 23 11 0.2 4 1:20 16 15 0.04 20 1:500 15 11 0.04 4 1:100 15 15

TABLE A19 in vitro-Test with Alternaria alternata (1.055) (3.030) (17.012) (5.013) mefen- (12.004) (15.016) metyltetra- Paenibacillus Colby (I-338) mancozeb trifluconazole metalaxyl-m metrafenone prole terrae Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 27 0.2 0 0.04 0 0.008 0 4 36 0.016 0 0.2 91 0.04 19 0.008 9 4 10 5 16 0.2 3 0.04 3 1 87 0.008 0 40 8 8 0 1.6 0 1 4 1:4 59 53 1 0.016 1:0.16 32 27 0.2 4 1:20 48 36 0.2 0.016 1:0.8 8 0 0.04 4 1:100 38 36 0.04 0.016 1:4 0 0 0.04 0.2 1:5 98 91 0.04 0.04 1:1 24 19 0.04 0.008 1:0.2 8 9 1 4 1:4 38 34 0.2 4 1:20 18 10 0.008 4 1:500 23 10 1 5 1:5 54 36 1 0.2 1:0.2 27 26 1 0.04 1:0.04 30 26 0.008 5 1:625 18 16 0.008 0.2 1:25 8 3 0.008 0.04 1:5 0 3 0.04 1 1:1 91 90 0.04 0.008 1:0.008 36 24 0.04 1 1:5 92 87 0.008 0.008 1:0.04 0 0 1 40 1:40 44 30 1 8 1:8 39 24 1 1.6 1:1.6 35 24

TABLE A20 in vitro-Test with Alternaria alternata (5.018) (13.004) (7.005) (3.020) Colby (I-338) propineb proquinazid pyrimethanil trifloxystrobin (I-130) (1.067) Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 52 0.2 10 0.04 4 0.008 0 20 65 4 43 0.8 14 2 4 0.4 3 0.08 0 0.8 96 0.16 10 0.2 85 0.04 49 1 100 0.2 100 0.008 25 2 74 0.2 20 1:100 74 68 0.2 4 1:20 49 49 0.2 0.8 1:4 26 22 0.04 20 1:500 74 66 0.04 4 1:100 71 45 0.04 0.8 1:20 20 17 0.008 20 1:2500 89 65 0.008 4 1:500 51 43 0.008 0.8 1:100 52 14 0.04 2 1:50 16 7 0.04 0.4 1:10 19 6 0.04 0.08 1:2 14 4 0.008 2 1:250 25 4 0.008 0.4 1:50 14 3 0.008 0.08 1:10 12 0 1 0.8 1:0.8 100 98 1 0.16 1:0.16 98 56 0.2 0.8 1:4 99 97 0.2 0.16 1:0.8 97 19 0.04 0.8 1:20 99 96 0.04 0.16 1:4 95 13 0.008 0.8 1:100 99 96 0.008 0.16 1:20 93 10 0.04 0.2 1:5 94 85 0.04 0.04 1:1 59 50 0.008 0.2 1:25 84 85 0.008 0.04 1:5 59 51 1 2 1:2 100 100 0.2 2 1:10 100 100 0.008 2 1:250 95 81

TABLE A21 in vitro-Test with Alternaria alternata (13.001) (2.005) (15.043) (3.012) (5.012) (15.012) Colby (I-130) fludioxonil fluopyram fluoxapiprolin fluoxastrobin folpet fosetylal Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 100 0.2 100 0.04 100 0.008 19 5 100 1 88 20 88 4 81 0.8 61 20 1 4 0 20 92 4 68 0.016 0 1 99 0.2 6 100 8 20 4 4 0 0.2 5 1:25 100 100 0.2 1 1:5 100 100 0.008 5 1:625 99 100 0.008 1 1:125 96 90 0.008 20 1:2500 91 91 0.008 4 1:500 85 85 0.008 0.8 1:100 73 69 0.04 20 1:500 100 100 0.04 4 1:100 100 100 0.008 20 1:2500 46 21 0.008 4 1:500 46 21 0.008 20 1:250 96 94 0.008 4 1:50 82 74 0.008 0.016 1:2 27 21 0.04 1 1:25 100 100 0.04 0.2 1:5 100 100 0.008 1 1:125 100 99 0.008 0.2 1:25 41 30 0.008 100 1:12500 53 32 0.008 20 1:2500 55 29 0.008 4 1:500 36 26

TABLE A22 in vitro-Test with Alternaria alternata (17.012) (6.002) (5.013) (15.016) Paenibacillus (2.017) Colby (I-130) isotianil mancozeb metra-fenone terrae penflufen Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 100 0.2 100 0.04 100 0.008 19 100 15 20 0 4 0 20 63 0.8 4 5 19 1 6 0.2 3 0.04 1 200 99 40 16 5 72 0.2 22 0.008 100 1:12500 50 44 0.008 20 1:2500 46 35 0.008 4 1:500 40 35 0.2 20 1:100 100 100 0.2 0.8 1:4 100 100 0.008 20 1:2500 90 76 0.008 0.8 1:100 47 37 0.04 5 1:125 100 100 0.04 1 1:25 100 99 0.04 0.2 1:5 100 99 0.04 0.04 1:1 99 99 0.008 5 1:625 57 47 0.008 1 1:125 62 38 0.008 0.2 1:25 51 37 0.008 0.04 1:5 42 35 0.04 200 1:5000 100 100 0.04 40 1:1000 100 100 0.008 200 1:25000 100 99 0.008 40 1:5000 66 45 0.2 5 1:25 100 100 0.2 0.2 1:1 100 100 0.008 5 1:625 85 82 0.008 0.2 1:25 73 49

TABLE B1 in vitro-Test with Botrytis cinerea (7.005) (2.005) (2.028) (2.038) Colby (I-052) pyrimethanil fluopyram inpyrfluxam isoflucypram Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 88 0.02 0 0.004 0 0.0008 0 20.0 100 4.0 100 0.8 100 0.16 0 20.0 100 4.0 72 0.8 69 0.16 30 1.0 87 0.2 69 0.04 66 0.008 4 1.0 75 0.2 74 0.04 58 0.008 10 0.02 20.0 1:1000 100 100 0.02 4.0 1:200 100 100 0.02 0.8 1:40 100 100 0.02 0.16 1:8 95 17 0.004 20.0 1:5000 100 100 0.004 4.0 1:1000 100 100 0.004 0.8 1:200 100 100 0.004 0.16 1:40 76 0 0.0008 20.0 1:25000 100 100 0.0008 4.0 1:5000 100 100 0.0008 0.8 1:1000 100 100 0.0008 0.16 1:200 24 8 0.02 20.0 1:1000 100 100 0.02 4.0 1:200 89 77 0.02 0.8 1:40 69 74 0.02 0.16 1:8 55 41 0.004 20.0 1:5000 100 100 0.004 4.0 1:1000 79 72 0.004 0.8 1:200 68 69 0.004 0.16 1:40 59 30 0.0008 20.0 1:25000 100 100 0.0008 4.0 1:5000 80 74 0.0008 0.8 1:1000 70 71 0.0008 0.16 1:200 51 35 0.004 1.0 1:250 89 87 0.004 0.2 1:50 79 69 0.004 0.04 1:10 58 66 0.004 0.008 1:2 31 4 0.0008 1.0 1:250 73 75 0.0008 0.2 1:50 74 74 0.0008 0.04 1:10 58 58 0.0008 0.008 1:2 27 10 0.004 1.0 1:1250 73 75 0.004 0.2 1:250 74 74 0.004 0.04 1:50 69 58 0.004 0.008 1:10 20 10

TABLE B2 in vitro-Test with Botrytis cinerea (3.025) (1.055) (1.021) (1.020) Colby (I-052) fenpicoxamid mefentrifluconazole tebuconazole spiroxamine Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 88 0.02 0 0.004 0 0.0008 0 1.0 21 0.2 6 0.04 6 0.2 78 0.04 37 0.008 0 1.0 94 0.2 37 0.04 0 0.008 0 20.0 18 4.0 0 0.8 0 0.16 0 0.02 1.0 1:50 37 21 0.02 0.2 1:10 12 6 0.02 0.04 1:2 13 6 0.004 1.0 1:250 31 21 0.004 0.2 1:50 9 6 0.004 0.04 1:10 0 6 0.0008 1.0 1:1250 38 21 0.0008 0.2 1:250 17 6 0.0008 0.04 1:50 4 6 0.02 0.2 1:10 99 78 0.02 0.04 1:2 81 37 0.02 0.008 1:0.4 46 0 0.004 0.2 1:50 99 78 0.004 0.04 1:10 100 37 0.004 0.008 1:2 71 0 0.0008 0.2 1:250 100 78 0.0008 0.04 1:50 100 37 0.0008 0.008 1:10 17 0 0.004 1.0 1:250 98 94 0.004 0.2 1:50 32 37 0.004 0.04 1:10 9 0 0.004 0.008 1:2 4 0 0.0008 1.0 1:1250 95 94 0.0008 0.2 1:250 52 37 0.0008 0.04 1:50 0 0 0.0008 0.008 1:10 19 0 0.1 20.0 1:200 84 83 0.1 4.0 1:40 100 79 0.1 0.8 1:8 100 79 0.1 0.16 1:1.6 100 79 0.004 20.0 1:5000 28 19 0.004 4.0 1:1000 0 1 0.004 0.8 1:200 0 1 0.004 0.16 1:40 0 1

TABLE B3 in vitro-Test with Botrytis cinerea (13.001) (13.004) (5.003) Colby (I-052) (15.064) fludioxonil proquinazid captan Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 88 0.02 0 0.004 0 0.0008 0 2.0 2 0.4 21 0.08 5 5.0 100 1.0 100 0.2 100 0.04 19 10.0 0 2.0 0 0.4 0 0.08 13 20.0 7 4.0 0 0.8 0 0.16 0 0.1 2.0 1:20 100 79 0.1 0.4 1:4 100 83 0.1 0.08 1:0.8 100 80 0.1 5.0 1:50 100 100 0.1 1.0 1:10 100 100 0.1 0.2 1:2 100 100 0.1 0.04 1:0.4 99 83 0.1 10.0 1:100 100 79 0.1 2.0 1:20 100 79 0.1 0.4 1:4 100 79 0.1 0.08 1:0.8 99 82 0.02 20.0 1:1000 27 7 0.02 4.0 1:200 0 0 0.02 0.8 1:40 0 0 0.02 0.16 1:8 0 0 0.0008 20.0 1:25000 77 7 0.0008 4.0 1:5000 0 0 0.0008 0.8 1:1000 0 0 0.0008 0.16 1:200 0 0

TABLE B4 in vitro-Test with Botrytis cinerea (5.010) (5.013) (5.018) Effi- Colby (I-052) dithianon mancozeb propineb cacy expected (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 88 0.02 0 0.004 0 0.0008 0 20.0 100 4.0 23 0.8 0 0.16 0 10.0 33 2.0 0 0.4 0 100.0 22 4.0 0 0.8 0 0.1 20.0 1:200 100 100 0.1 4.0 1:40 100 81 0.1 0.8 1:8 68 75 0.1 0.16 1:1.6 87 75 0.02 20.0 1:1000 100 100 0.02 4.0 1:200 40 23 0.02 0.8 1:40 0 0 0.02 0.16 1:8 0 0 0.004 20.0 1:5000 100 100 0.004 4.0 1:1000 37 23 0.004 0.8 1:200 25 0 0.004 0.16 1:40 0 0 0.0008 20.0 1:25000 100 100 0.0008 4.0 1:5000 35 23 0.0008 0.8 1:1000 0 0 0.0008 0.16 1:200 5 0 0.1 10.0 1:100 100 92 0.1 2.0 1:20 99 88 0.1 0.4 1:4 81 88 0.02 10.0 1:500 52 40 0.02 2.0 1:100 30 12 0.02 0.4 1:20 0 12 0.004 10.0 1:2500 33 33 0.004 2.0 1:500 16 0 0.004 0.4 1:100 0 0 0.1 100.0 1:1000 100 90 0.1 4.0 1:40 86 88 0.1 0.8 1:8 100 88 0.0008 100.0 1:125000 31 22 0.0008 4.0 1:5000 20 0 0.0008 0.8 1:1000 13 0

TABLE B5 in vitro-Test with Botrytis cinerea (7.005) (2.002) (2.005) (2.038) Colby (I-300) pyrimethanil bixafen fluopyram isoflucypram Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 49 0.02 0 0.004 0 0.0008 0 20.0 100 4.0 100 0.8 76 0.16 3 1.0 67 0.2 63 0.04 22 20.0 86 4.0 72 0.8 67 0.16 35 0.2 71 0.04 64 0.008 7 0.02 20.0 1:1000 100 100 0.02 4.0 1:200 100 100 0.02 0.8 1:40 100 76 0.02 0.16 1:8 24 3 0.004 20.0 1:5000 100 100 0.004 4.0 1:1000 100 100 0.004 0.8 1:200 100 76 0.004 0.16 1:40 10 3 0.02 1.0 1:50 81 67 0.02 0.2 1:10 66 63 0.02 0.04 1:2 38 22 0.004 1.0 1:250 73 67 0.004 0.2 1:50 70 63 0.004 0.04 1:10 16 22 0.02 20.0 1:5000 99 86 0.02 4.0 1:1000 83 72 0.02 0.8 1:200 66 67 0.02 0.16 1:40 39 35 0.1 0.2 1:2 100 88 0.1 0.04 1:0.4 100 85 0.1 0.008 1:0.08 98 62 0.004 0.2 1:50 77 72 0.004 0.04 1:10 67 66 0.004 0.008 1:2 25 12

TABLE B6 in vitro-Test with Botrytis cinerea (3.025) (3.020) (1.002) (1.055) fenpi- trifloxy- difeno- mefentriflu- Colby (I-300) coxamid strobin conazole conazole Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 49 0.02 0 0.004 0 0.0008 0 5.0 45 1.0 15 0.2 9 0.04 15 1.0 37 0.2 0 0.04 0 0.008 19 1.0 0 0.2 0 0.04 0 0.008 8 1.0 100 0.2 53 0.04 0 0.008 0 0.1 5.0 1:50 97 77 0.1 1.0 1:10 92 65 0.1 0.2 1:2 95 63 0.1 0.04 1:0.4 98 65 0.1 1.0 1:10 90 74 0.1 0.2 1:2 86 59 0.1 0.04 1:0.4 78 59 0.1 0.008 1:0.08 69 67 0.1 1.0 1:10 85 59 0.1 0.2 1:2 73 59 0.1 0.04 1:0.4 100 59 0.1 0.008 1:0.08 100 62 0.02 1.0 1:50 100 100 0.02 0.2 1:10 81 53 0.02 0.04 1:2 0 0 0.02 0.008 1:0.4 0 0 0.004 1.0 1:250 100 100 0.004 0.2 1:50 75 53 0.004 0.04 1:10 0 0 0.004 0.008 1:2 0 0

TABLE B7 in vitro-Test with Botrytis cinerea (1.018) (1.021) (1.020) Colby (I-300) prothioconazole tebuconazole spiroxamine (15.064) Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 49 0.02 0 0.004 0 0.0008 0 1.0 100 0.2 94 0.04 48 0.008 0 1.0 100 0.2 45 0.04 0 0.008 0 4.0 8 0.8 0 0.16 0 2.0 5 0.4 0 0.08 9 0.0008 1.0 1:1250 100 100 0.0008 0.2 1:250 99 94 0.0008 0.04 1:50 44 48 0.0008 0.008 1:10 0 0 0.1 1.0 1:10 100 100 0.1 0.2 1:2 80 72 0.1 0.04 1:0.4 73 49 0.1 0.008 1:0.08 98 49 0.1 4.0 1:40 100 78 0.1 0.8 1:8 82 77 0.1 0.16 1:1.6 85 77 0.0008 4.0 1:5000 4 8 0.0008 0.8 1:1000 25 0 0.0008 0.16 1:200 0 0 0.1 2.0 1:20 100 78 0.1 0.4 1:4 100 77 0.1 0.08 1:0.8 84 79 0.0008 2.0 1:2500 8 5 0.0008 0.4 1:500 0 0 0.0008 0.08 1:100 11 9

TABLE B8 in vitro-Test with Botrytis cinerea (13.001) (13.004) (13.005) (5.003) Colby (I-300) fludioxonil proquinazid quinoxyfen captan Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 49 0.02 0 0.004 0 0.0008 0 5.0 100 1.0 100 0.2 100 0.04 16 10.0 0 2.0 14 0.4 0 0.08 2 10.0 0 2.0 0 0.4 0 0.08 24 20.0 100 4.0 26 0.8 0 0.16 0 0.1 5.0 1:50 100 100 0.1 1.0 1:10 100 100 0.1 0.2 1:2 100 100 0.1 0.04 1:0.4 100 80 0.1 10.0 1:100 100 77 0.1 2.0 1:20 100 80 0.1 0.4 1:4 98 77 0.1 0.08 1:0.8 98 77 0.1 10.0 1:100 100 46 0.1 2.0 1:20 95 46 0.1 0.4 1:4 97 46 0.1 0.08 1:0.8 77 59 0.1 20.0 1:200 100 100 0.1 4.0 1:40 100 60 0.1 0.8 1:8 100 46 0.1 0.16 1:1.6 97 46

TABLE B9 in vitro-Test with Botrytis cinerea (5.010) (5.012) (5.013) (5.018) Colby (I-300) dithianon folpet mancozeb propineb Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 49 0.02 0 0.004 0 0.0008 0 20.0 99 4.0 15 0.8 0 0.16 26 10.0 100 2.0 100 0.4 0 0.08 0 100.0 83 20.0 15 4.0 0 0.8 15 100.0 83 20.0 15 4.0 0 0.8 15 0.1 20.0 1:200 100 100 0.1 4.0 1:40 100 54 0.1 0.8 1:8 100 46 0.1 0.16 1:1.6 99 60 0.1 10.0 1:100 100 100 0.1 2.0 1:20 100 100 0.1 0.4 1:4 100 46 0.1 0.08 1:0.8 79 46 0.0008 10.0 1:12500 99 100 0.0008 2.0 1:2500 100 100 0.0008 0.4 1:500 0 0 0.0008 0.08 1:100 15 0 0.1 100.0 1:100 100 78 0.1 20.0 1:20 90 64 0.1 4.0 1:4 79 59 0.1 0.8 1:0.8 82 61 0.0008 100.0 1:12500 64 47 0.0008 20.0 1:2500 13 13 0.0008 4.0 1:500 14 1 0.0008 0.8 1:100 8 7 0.1 100.0 1:1000 100 93 0.1 20.0 1:200 62 64 0.1 4.0 1:40 57 58 0.1 0.8 1:8 74 65 0.0008 100.0 1:125000 95 83 0.0008 20.0 1:25000 15 15 0.0008 4.0 1:5000 0 0 0.0008 0.8 1:1000 7 15

TABLE B10 in vitro-Test with Botrytis cinerea (17.001) (15.016) Bacillus (17.012) (18.001) Colby (I-300) metrafenone subtilis Paenibacillus FLiPPER Efficacy expected (ppm) (ppm) (ppm) terrae (ppm) (ppm) Ratio % value % 0.1 49 0.02 0 0.004 0 0.0008 0 20.0 0 4.0 0 0.8 18 0.16 15 200.0 23 40.0 0 8.0 0 1.6 0 200.0 100 40.0 13 8.0 13 1.6 0 200.0 0 40.0 1 8.0 6 1.6 0 0.1 20.0 1:200 99 58 0.1 4.0 1:40 71 58 0.1 0.8 1:8 77 66 0.1 0.16 1:1.6 67 65 0.1 200.0 1:2000 85 73 0.1 40.0 1:400 74 64 0.1 8.0 1:80 91 64 0.1 1.6 1:16 58 64 0.0008 200.0 1:2000 100 100 0.0008 40.0 1:400 79 69 0.0008 8.0 1:80 99 69 0.0008 1.6 1:16 69 64 0.1 200.0 1:2000 82 64 0.1 40.0 1:400 100 65 0.1 8.0 1:80 77 67 0.1 1.6 1:16 66 64

TABLE B11 in vitro-Test with Botrytis cinerea (7.005) (2.005) (2.028) (2.038) Colby (I-302) pyrimethanil fluopyram inpyrfluxam isoflucypram Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 88 0.02 2 0.004 0 0.0008 0 20.0 100 4.0 100 0.8 100 0.16 22 20.0 75 4.0 75 0.8 65 0.16 5 0.2 71 0.04 48 0.008 4 1.0 77 0.2 58 0.04 53 0.008 5 0.02 20.0 1:1000 100 100 0.02 4.0 1:200 100 100 0.02 0.8 1:40 100 100 0.02 0.16 1:8 68 24 0.004 20.0 1:5000 100 100 0.004 4.0 1:1000 100 100 0.004 0.8 1:200 100 100 0.004 0.16 1:40 54 34 0.1 20.0 1:200 98 97 0.1 4.0 1:40 99 97 0.1 0.8 1:8 98 96 0.1 0.16 1:1.6 100 90 0.0008 20.0 1:25000 89 75 0.0008 4.0 1:5000 78 75 0.0008 0.8 1:1000 68 65 0.0008 0.16 1:200 30 5 0.1 0.2 1:2 98 97 0.1 0.04 1:0.4 100 94 0.1 0.008 1:0.08 100 89 0.0008 0.2 1:250 74 71 0.0008 0.04 1:50 42 48 0.0008 0.008 1:10 12 4 0.1 1.0 1:10 100 97 0.1 0.2 1:2 100 95 0.1 0.04 1:0.4 98 94 0.1 0.008 1:0.08 100 88 0.0008 1.0 1:1250 73 77 0.0008 0.2 1:250 66 58 0.0008 0.04 1:50 52 53 0.0008 0.008 1:10 21 5

TABLE B12 in vitro-Test with Botrytis cinerea (1.020) (13.001) (13.004) (13.005) Colby (I-302) spiroxamine fludioxonil proquinazid quinoxyfen Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 88 0.02 2 0.004 0 0.0008 0 20.0 14 4.0 0 0.8 0 0.16 0 5.0 100 1.0 100 0.2 100 0.04 0 10.0 0 2.0 0 0.4 0 0.08 13 10.0 7 2.0 2 0.4 0 0.08 0 0.1 20.0 1:200 75 80 0.1 4.0 1:40 85 77 0.1 0.8 1:8 85 77 0.1 0.16 1:1.6 100 77 0.004 20.0 1:5000 18 14 0.004 4.0 1:1000 0 0 0.004 0.8 1:200 18 0 0.004 0.16 1:40 0 0 0.1 5.0 1:50 100 100 0.1 1.0 1:10 100 100 0.1 0.2 1:2 100 100 0.1 0.04 1:0.4 100 77 0.02 5.0 1:250 100 100 0.02 1.0 1:50 100 100 0.02 0.2 1:10 100 100 0.02 0.04 1:2 59 0 0.1 10.0 1:100 88 77 0.1 2.0 1:20 100 77 0.1 0.4 1:4 92 77 0.1 0.08 1:0.8 99 80 0.02 10.0 1:500 0 0 0.02 2.0 1:100 8 0 0.02 0.4 1:20 46 0 0.02 0.08 1:4 58 13 0.1 10.0 1:100 99 82 0.1 2.0 1:20 100 81 0.1 0.4 1:4 100 80 0.1 0.08 1:0.8 100 80

TABLE B13 in vitro-Test with Botrytis cinerea (5.003) (5.010) (5.012) (5.018) Colby (I-302) captan dithianon folpet propineb Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 88 0.02 2 0.004 0 0.0008 0 20.0 100 4.0 100 0.8 0 0.16 0 20.0 100 4.0 100 0.8 0 0.16 0 10.0 100 2.0 100 0.4 8 0.08 8 100.0 86 4.0 0 0.8 16 0.1 20.0 1:200 100 100 0.1 4.0 1:40 100 100 0.1 0.8 1:8 100 80 0.1 0.16 1:1.6 100 80 0.0008 20.0 1:25000 100 100 0.0008 4.0 1:5000 100 100 0.0008 0.8 1:1000 0 0 0.0008 0.16 1:200 16 0 0.1 20.0 1:200 100 100 0.1 4.0 1:40 100 100 0.1 0.8 1:8 100 80 0.1 0.16 1:1.6 100 80 0.0008 20.0 1:25000 100 100 0.0008 4.0 1:5000 100 100 0.0008 0.8 1:1000 9 0 0.0008 0.16 1:200 13 0 0.1 10.0 1:100 100 100 0.1 2.0 1:20 100 100 0.1 0.4 1:4 100 82 0.1 0.08 1:0.8 98 82 0.0008 10.0 1:12500 100 100 0.0008 2.0 1:2500 100 100 0.0008 0.4 1:500 10 8 0.0008 0.08 1:100 15 8 0.1 100.0 1:1000 100 99 0.1 4.0 1:40 100 93 0.1 0.8 1:8 100 94 0.0008 100.0 1:125000 91 86 0.0008 4.0 1:5000 0 0 0.0008 0.8 1:1000 12 16

TABLE B14 in vitro-Test with Botrytis cinerea (15.012) (15.016) (17.012) Colby (I-302) fosetylaluminium metrafenone Paenibacillus Efficacy expected (ppm) (ppm) (ppm) terrae (ppm) Ratio % value % 0.1 88 0.02 2 0.004 0 0.0008 0 100.0 1 4.0 13 0.8 0 20.0 0 0.8 0 0.16 0 200.0 94 40.0 2 0.1 100.0 1:1000 100 93 0.1 4.0 1:40 96 93 0.1 0.8 1:8 97 93 0.0008 100.0 1:125000 0 1 0.0008 4.0 1:5000 17 13 0.0008 0.8 1:1000 23 0 0.1 20.0 1:200 100 93 0.1 0.8 1:8 99 93 0.1 0.16 1:1.6 100 93 0.0008 20.0 1:25000 0 0 0.0008 0.8 1:1000 0 0 0.0008 0.16 1:200 22 0 0.1 200.0 1:2000 100 100 0.1 40.0 1:400 100 100 0.02 200.0 1:10000 100 95 0.02 40.0 1:2000 37 22 0.004 200.0 1:50000 94 94 0.004 40.0 1:10000 0 2 0.0008 200.0 1:250000 94 88 0.0008 40.0 1:50000 0 2

TABLE B15 in vitro-Test with Botrytis cinerea (1.002) (3.025) (2.005) (15.043) (2.002) difeno- fenpicox- fluo- fluoxa- (5.012) Colby (I-338) bixafen conazole amid pyram piprolin folpet Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 100 0.2 0 0.04 8 0.008 0 1 66 0.2 0 0.008 6 1 13 1 52 0.2 14 0.008 0 20 100 4 79 0.8 51 0.16 0 0.16 1 1 16 0.04 1 0.008 8 0.008 1 1:125 70 67 0.008 0.2 1:25 25 21 0.008 0.008 1:1 40 7 0.2 1 1:5 26 13 0.04 1 1:25 31 13 0.008 1 1:125 27 13 0.008 1 1:125 56 52 0.008 0.2 1:25 20 14 0.008 0.008 1:1 33 0 0.04 20 1:500 99 100 0.04 4 1:100 84 79 0.04 0.8 1:20 57 51 0.04 0.16 1:4 6 0 1 0.16 1:0.16 100 94 0.04 0.16 1:4 1 1 0.008 0.16 1:20 4 1 1 1 1:1 100 87 1 0.04 1:0.04 88 85 1 0.008 1:0.008 92 86 0.008 1 1:125 24 16 0.008 0.04 1:5 5 1 0.008 0.008 1:1 7 8

TABLE B16 in vitro-Test with Botrytis cinerea (1.055) (2.028) (2.038) (5.013) mefen- (3.030) (15.012) inpyr- isoflucy- manco- triflu- metyl- Colby (I-338) fosetyl-al fluxam pram zeb conazole tetraprole Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 85 0.2 0 0.04 0 0.008 0 100 0 4 2 1 71 0.2 52 1 70 0.2 53 20 0 0.8 0 0.16 0 0.2 30 0.04 0 0.008 0 1 33 0.2 7 0.04 11 0.008 7 1 100 1:100 100 85 1 4 1:4 87 85 0.008 100 1:12500 0 0 0.008 4 1:500 8 2 0.2 1 1:5 73 71 0.2 0.2 1:1 51 52 0.008 1 1:125 72 71 0.008 0.2 1:25 53 52 0.2 1 1:5 77 70 0.2 0.2 1:1 56 53 0.04 1 1:25 74 70 0.04 0.2 1:5 53 53 0.008 1 1:125 76 70 0.008 0.2 1:25 53 53 0.008 20 1:2500 98 0 0.008 0.8 1:100 0 0 0.008 0.16 1:20 1 0 0.2 0.2 1:1 76 30 0.2 0.04 1:0.2 5 0 0.2 0.008 1:0.04 0 0 0.04 1 1:25 36 35 0.04 0.2 1:5 25 11 0.04 0.04 1:1 21 14 0.04 0.008 1:0.2 15 10

TABLE B17 in vitro-Test with Botrytis cinerea (2.017) (5.018) (13.004) (7.005) (13.005) Colby (I-338) penflufen propineb proquinazid pyrimethanil quinoxyfen Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 74 0.2 13 0.04 6 0.008 3 5 70 0.04 0 100 8 20 0 4 5 10 16 2 3 0.4 0 4 95 0.8 89 0.16 16 0.4 0 0.08 0 0.04 5 1:125 74 71 0.04 0.04 1:1 1 4 0.008 5 1:625 77 70 0.008 0.04 1:5 7 0 1 100 1:100 100 76 1 20 1:20 100 74 1 4 1:4 100 75 1 10 1:10 100 78 1 2 1:2 91 75 1 0.4 1:0.4 95 74 0.2 4 1:20 100 96 0.2 0.8 1:4 93 90 0.2 0.16 1:0.8 85 27 0.04 4 1:100 100 95 0.04 0.8 1:20 96 90 0.04 0.16 1:4 90 21 0.008 4 1:500 97 95 0.008 0.8 1:100 87 89 0.008 0.16 1:20 89 19 0.04 0.4 1:10 8 0 0.04 0.08 1:2 16 0 0.008 0.4 1:50 8 5 0.008 0.08 1:10 12 5

TABLE B18 in vitro-Test with Botrytis cinerea (15.043) (3.012) (1.062) (5.013) (12.004) (13.004) fluoxa- fluoxa- fluoxytio- manco- meta- pro- Colby (I-130) piprolin strobin conazole zeb laxyl-m quinazid Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 100 0.2 100 0.04 100 0.008 96 20 5 4 6 0.8 0 2 31 0.4 20 0.016 0 1 13 0.2 0 0.008 0 20 15 0.8 4 0.16 0 100 13 20 4 4 3 0.8 5 10 0 2 5 0.4 0 0.008 20 1:2500 100 96 0.008 4 1:500 100 96 0.008 0.8 1:100 100 96 0.008 2 1:250 100 97 0.008 0.4 1:50 100 97 0.008 0.016 1:2 97 96 0.008 1 1:125 100 97 0.008 0.2 1:25 100 96 0.008 0.008 1:1 97 96 0.008 20 1:2500 91 86 0.008 0.8 1:100 99 85 0.008 0.16 1:20 100 84 0.008 100 1:12500 100 86 0.008 20 1:2500 99 85 0.008 4 1:500 98 84 0.008 0.8 1:100 98 85 0.008 10 1:1250 61 34 0.008 2 1:250 65 37 0.008 0.4 1:50 49 34

TABLE C1 in vitro-Test with Cercospora beticola (1.002) (7.005) (2.005) (3.025) difeno- Colby (I-052) pyrimethanil fluopyram fenpicoxamid conazole Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 20 0.02 0 0.004 0 0.0008 0 20.0 100 4.0 98 0.8 10 0.16 11 20.0 39 4.0 27 0.8 0 0.16 3 5.0 92 1.0 62 0.2 41 0.04 0 1.0 99 0.2 79 0.02 20.0 1:1000 100 100 0.02 4.0 1:200 92 98 0.02 0.8 1:40 24 10 0.02 0.16 1:8 16 11 0.0008 20.0 1:25000 100 100 0.0008 4.0 1:5000 99 98 0.0008 0.8 1:1000 11 10 0.0008 0.16 1:200 18 11 0.0008 20.0 1:25000 50 39 0.0008 4.0 1:5000 30 27 0.0008 0.8 1:1000 22 0 0.0008 0.16 1:200 18 3 0.1 5.0 1:50 96 94 0.1 1.0 1:10 81 69 0.1 0.2 1:2 78 53 0.1 0.04 1:0.4 20 20 0.1 1.0 1:10 99 100 0.1 0.2 1:2 90 83 0.02 1.0 1:50 100 99 0.02 0.2 1:10 81 79 0.004 1.0 1:250 100 99 0.004 0.2 1:50 91 79 0.0008 1.0 1:1250 100 99 0.0008 0.2 1:250 99 79

TABLE C2 in vitro-Test with Cercospora beticola (1.055) Colby mefen- (1.018) (13.001) expec- triflu- prothio- fludio- (5.003) Effi- ted (I-052) conazole conazole xonil captan cacy value (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % % 0.1 20 0.02 0 0.004 0 0.0008 0 1.0 100 0.2 100 0.04 100 0.008 60 1.0 100 0.2 100 0.04 22 0.008 21 5.0 93 1.0 44 0.2 14 20.0 57 4.0 45 0.8 0 0.02 1.0 1:50 100 100 0.02 0.2 1:10 100 100 0.02 0.04 1:2 100 100 0.02 0.008 1:0.4 79 60 0.004 1.0 1:250 100 100 0.004 0.2 1:50 100 100 0.004 0.04 1:10 100 100 0.004 0.008 1:2 95 69 0.0008 1.0 1:1250 100 100 0.0008 0.2 1:250 100 100 0.0008 0.04 1:50 100 100 0.0008 0.008 1:10 88 62 0.1 1.0 1:10 100 100 0.1 0.2 1:2 98 100 0.1 0.04 1:0.4 45 22 0.1 0.008 1:0.08 26 21 0.0008 1.0 1:1250 100 100 0.0008 0.2 1:250 100 100 0.0008 0.04 1:50 86 27 0.0008 0.008 1:10 50 25 0.1 5.0 1:50 100 94 0.1 1.0 1:10 95 51 0.1 0.2 1:2 37 26 0.02 5.0 1:250 92 93 0.02 1.0 1:50 88 44 0.02 0.2 1:10 56 14 0.0008 5.0 1:6250 95 93 0.0008 1.0 1:1250 78 49 0.0008 0.2 1:250 51 22 0.02 20.0 1:1000 74 61 0.02 4.0 1:200 72 50 0.02 0.8 1:40 23 11 0.004 20.0 1:5000 100 57 0.004 4.0 1:1000 100 45 0.004 0.8 1:200 8 0

TABLE C3 in vitro-Test with Cercospora beticola (5.010) (5.013) (5.018) (17.012) Colby (I-052) dithianon mancozeb propineb Paenibacillus Efficacy expected (ppm) (ppm) (ppm) (ppm) terrae (ppm) Ratio % value % 0.1 20 0.02 0 0.004 0 0.0008 0 20.0 99 4.0 100 0.8 0 10.0 100 2.0 100 0.4 0 0.08 0 100.0 100 20.0 100 4.0 100 0.8 0 200.0 100 40.0 30 8.0 0 1.6 6 0.1 20.0 1:200 100 99 0.1 4.0 1:40 100 100 0.1 0.8 1:8 28 19 0.004 20.0 1:5000 100 99 0.004 4.0 1:1000 100 100 0.004 0.8 1:200 30 0 0.1 10.0 1:100 100 100 0.1 2.0 1:20 100 100 0.1 0.4 1:4 84 2 0.1 0.08 1:0.8 6 2 0.004 10.0 1:2500 100 100 0.004 2.0 1:500 100 100 0.004 0.4 1:100 0 0 0.004 0.08 1:20 0 0 0.1 100.0 1:1000 100 100 0.1 20.0 1:200 100 100 0.1 4.0 1:40 100 100 0.1 0.8 1:8 69 2 0.004 100.0 1:25000 100 100 0.004 20.0 1:5000 100 100 0.004 4.0 1:1000 100 100 0.004 0.8 1:200 33 0 0.1 200.0 1:2000 100 100 0.1 40.0 1:400 41 30 0.1 8.0 1:80 28 0 0.1 1.6 1:16 6 6

TABLE C4 in vitro-Test with Cercospora beticola Colby (2.038) (3.025) (3.020) (1.002) expect- isoflu- fenpi- trifloxy- difeno- Effi- ed (I-300) cypram coxamid strobin conazole cacy value (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % % 0.1 19 0.02 10 0.004 0 0.0008 0 1.0 69 0.2 44 0.04 0 0.008 10 5.0 88 1.0 53 0.2 35 0.04 14 1.0 100 0.2 100 0.04 100 0.008 95 1.0 100 0.2 71 0.04 20 0.008 5 0.1 1.0 1:10 83 69 0.1 0.2 1:2 58 44 0.1 0.04 1:0.4 0 0 0.1 0.008 1:0.08 0 10 0.1 5.0 1:50 94 88 0.1 1.0 1:10 84 53 0.1 0.2 1:2 82 35 0.1 0.04 1:0.4 55 14 0.02 1.0 1:50 100 100 0.02 0.2 1:10 100 100 0.02 0.04 1:2 100 100 0.02 0.008 1:0.4 100 95 0.004 1.0 1:250 100 100 0.004 0.2 1:50 100 100 0.004 0.04 1:10 100 100 0.004 0.008 1:2 99 95 0.02 1.0 1:50 100 100 0.02 0.2 1:10 98 73 0.02 0.04 1:2 57 25 0.02 0.008 1:0.4 31 11 0.0008 1.0 1:1250 99 100 0.0008 0.2 1:250 94 71 0.0008 0.04 1:50 44 20 0.0008 0.008 1:10 6 5

TABLE C5 in vitro-Test with Cercospora beticola (1.055) Colby mefen- (1.018) (1.021) (13.001) expec- triflu- prothio- tebu- fludio- Effi- ted (I-300) conazole conazole conazole xonil cacy value (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % % 0.1 19 0.02 10 0.004 0 0.0008 0 1.0 100 0.2 100 0.04 91 0.008 80 1.0 100 0.2 98 0.04 88 0.008 10 1.0 100 0.2 100 0.04 32 0.008 12 5.0 98 1.0 99 0.2 14 0.04 0 0.1 1.0 1:10 100 100 0.1 0.2 1:2 100 100 0.1 0.04 1:0.4 100 91 0.1 0.008 1:0.08 97 80 0.02 1.0 1:50 100 100 0.02 0.2 1:10 100 100 0.02 0.04 1:2 100 91 0.02 0.008 1:0.4 96 80 0.1 1.0 1:10 100 100 0.1 0.2 1:2 100 98 0.1 0.04 1:0.4 87 88 0.1 0.008 1:0.08 11 10 0.02 1.0 1:50 100 100 0.02 0.2 1:10 100 98 0.02 0.04 1:2 93 88 0.02 0.008 1:0.4 10 10 0.02 1.0 1:50 100 100 0.02 0.2 1:10 92 100 0.02 0.04 1:2 71 32 0.02 0.008 1:0.4 10 12 0.004 5.0 1:1250 94 98 0.004 1.0 1:250 99 99 0.004 0.2 1:50 44 14 0.004 0.04 1:10 26 0

TABLE C6 in vitro-Test with Cercospora beticola (13.004) (13.005) (5.003) (5.010) Colby (I-300) proquinazid quinoxyfen captan dithianon Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 19 0.02 10 0.004 0 0.0008 0 10.0 19 2.0 0 0.4 0 0.08 9 10.0 34 2.0 4 0.4 0 0.08 10 20.0 25 4.0 13 0.8 0 20.0 99 4.0 99 0.8 28 0.16 12 0.1 10.0 1:500 28 19 0.1 2.0 1:100 27 0 0.1 0.4 1:20 27 0 0.1 0.08 1:4 10 9 0.1 10.0 1:100 59 34 0.1 2.0 1:20 23 4 0.1 0.4 1:4 0 0 0.1 0.08 1:0.8 18 10 0.1 20.0 1:200 100 25 0.1 4.0 1:40 28 13 0.1 0.8 1:8 19 0 0.02 20.0 1:1000 99 30 0.02 4.0 1:200 25 19 0.02 0.8 1:40 0 7 0.1 20.0 1:200 98 99 0.1 4.0 1:40 99 99 0.1 0.8 1:8 41 28 0.1 0.16 1:1.6 17 12

TABLE C7 in vitro-Test with Cercospora beticola (5.012) (5.013) (5.018) (15.016) Colby (I-300) folpet mancozeb propineb metrafenone Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 19 0.02 10 0.004 0 0.0008 0 10.0 100 2.0 100 0.4 50 0.08 14 10.0 100 2.0 100 0.4 19 0.08 4 100.0 100 20.0 100 4.0 100 0.8 34 20.0 0 4.0 0 0.8 10 0.16 14 0.1 10.0 1:100 100 100 0.1 2.0 1:20 99 100 0.1 0.4 1:4 96 50 0.1 0.08 1:0.8 21 14 0.02 10.0 1:500 100 100 0.02 2.0 1:100 100 100 0.02 0.4 1:20 95 53 0.02 0.08 1:4 21 20 0.1 10.0 1:100 100 100 0.1 2.0 1:20 100 100 0.1 0.4 1:4 100 34 0.1 0.08 1:0.8 25 22 0.004 10.0 1:2500 100 100 0.004 2.0 1:500 100 100 0.004 0.4 1:100 75 19 0.004 0.08 1:20 0 4 0.1 100.0 1:1000 100 100 0.1 20.0 1:200 100 100 0.1 4.0 1:40 100 100 0.1 0.8 1:8 100 46 0.02 100.0 1:5000 100 100 0.02 20.0 1:1000 100 100 0.02 4.0 1:200 100 100 0.02 0.8 1:40 100 40 0.004 100.0 1:25000 100 100 0.004 20.0 1:5000 100 100 0.004 4.0 1:1000 100 100 0.004 0.8 1:200 100 34 0.0008 100.0 1:125000 100 100 0.0008 20.0 1:25000 100 100 0.0008 4.0 1:5000 100 100 0.0008 0.8 1:1000 69 34 0.0008 20.0 1:25000 53 0 0.0008 4.0 1:5000 30 0 0.0008 0.8 1:1000 9 10 0.0008 0.16 1:200 15 14

TABLE C8 in vitro-Test with Cercospora beticola (7.005) (2.002) (2.028) (3.025) Colby (I-302) pyrimethanil bixafen inpyrfluxam fenpicoxamid Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 35 0.02 31 0.004 0 0.0008 0 20.0 100 4.0 100 0.8 20 0.16 0 1.0 0 0.2 0 1.0 11 0.2 8 0.04 16 0.008 25 5.0 98 1.0 20 0.2 2 0.04 0 0.02 20.0 1:1000 100 100 0.02 4.0 1:200 100 100 0.02 0.8 1:40 30 23 0.02 0.16 1:8 0 5 0.1 1.0 1:10 55 0 0.1 0.2 1:2 17 0 0.02 1.0 1:50 34 5 0.02 0.2 1:10 24 5 0.004 1.0 1:250 38 0 0.004 0.2 1:50 30 0 0.0008 1.0 1:1250 8 2 0.0008 0.2 1:250 0 2 0.004 1.0 1:250 19 11 0.004 0.2 1:50 12 8 0.004 0.04 1:10 21 16 0.004 0.008 1:2 26 25 0.1 5.0 1:50 98 98 0.1 1.0 1:10 100 24 0.1 0.2 1:2 71 8 0.1 0.04 1:0.4 25 6 0.02 5.0 1:250 100 98 0.02 1.0 1:50 72 20 0.02 0.2 1:10 9 2 0.02 0.04 1:2 9 0 0.004 5.0 1:1250 100 98 0.004 1.0 1:250 76 26 0.004 0.2 1:50 10 10 0.004 0.04 1:10 2 8 0.0008 5.0 1:6250 100 98 0.0008 1.0 1:1250 65 26 0.0008 0.2 1:250 0 10 0.0008 0.04 1:50 14 8

TABLE C9 in vitro-Test with Cercospora beticola (1.055) Colby (1.002) mefen- (1.018) (13.001) expec- difeno- triflu- prothio- fludio- Effi- ted (I-302) conazole conazole conazole xonil cacy value (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % % 0.1 35 0.02 31 0.004 0 0.0008 0 1.0 99 0.2 89 0.04 40 0.008 15 1.0 100 0.2 100 0.04 100 0.008 12 1.0 100 0.2 100 0.04 38 0.008 6 5.0 90 1.0 55 0.04 0 0.1 1.0 1:10 99 99 0.1 0.2 1:2 92 90 0.1 0.04 1:0.4 48 43 0.1 0.008 1:0.08 46 20 0.02 1.0 1:50 100 99 0.02 0.2 1:10 83 89 0.02 0.04 1:2 53 40 0.02 0.008 1:0.4 21 15 0.02 1.0 1:50 100 100 0.02 0.2 1:10 100 100 0.02 0.04 1:2 98 100 0.02 0.008 1:0.4 63 31 0.004 1.0 1:250 100 100 0.004 0.2 1:50 100 100 0.004 0.04 1:10 100 100 0.004 0.008 1:2 15 12 0.0008 1.0 1:1250 100 100 0.0008 0.2 1:250 100 100 0.0008 0.04 1:50 100 100 0.0008 0.008 1:10 57 12 0.1 1.0 1:10 100 100 0.1 0.2 1:2 98 100 0.1 0.04 1:0.4 83 38 0.1 0.008 1:0.08 28 6 0.1 5.0 1:50 98 90 0.1 1.0 1:10 49 55 0.1 0.04 1:0.4 36 0 0.02 5.0 1:250 98 91 0.02 1.0 1:50 98 59 0.02 0.04 1:2 24 10 0.004 5.0 1:1250 100 92 0.004 1.0 1:250 100 64 0.004 0.04 1:10 2 21 0.0008 5.0 1:6250 94 91 0.0008 1.0 1:1250 80 58 0.0008 0.04 1:50 17 8

TABLE C10 in vitro-Test with Cercospora beticola (5.010) (5.013) (5.003) dithia- (5.012) man- (17.012) (18.001) Colby (I-302) captan non folpet cozeb Paenibacillus FLiPPER Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) terrae (ppm) (ppm) Ratio % value % 0.1 35 0.02 31 0.004 0 0.0008 0 20.0 100 4.0 100 0.8 0 0.16 0 20.0 99 4.0 100 0.8 0 0.16 0 10.0 100 2.0 100 0.4 0 0.08 0 10.0 100 2.0 100 0.4 83 0.08 0 200.0 100 40.0 43 8.0 0 1.6 1 200.0 17 40.0 35 8.0 25 1.6 0 0.004 20.0 1:5000 100 100 0.004 4.0 1:1000 100 100 0.004 0.8 1:200 0 0 0.004 0.16 1:40 37 0 0.0008 20.0 1:25000 100 100 0.0008 4.0 1:5000 100 100 0.0008 0.8 1:1000 14 0 0.0008 0.16 1:200 4 0 0.1 20.0 1:200 100 99 0.1 4.0 1:40 100 100 0.1 0.8 1:8 39 0 0.1 0.16 1:1.6 0 0 0.0008 20.0 1:25000 100 99 0.0008 4.0 1:5000 100 100 0.0008 0.8 1:1000 14 0 0.0008 0.16 1:200 0 0 0.0008 10.0 1:100 100 100 0.0008 2.0 1:20 100 100 0.0008 0.4 1:4 21 0 0.0008 0.08 1:0.8 0 0 0.1 10.0 1:100 99 100 0.1 2.0 1:20 100 100 0.1 0.4 1:4 87 89 0.1 0.08 1:0.8 40 35 0.02 200.0 1:10000 100 100 0.02 40.0 1:2000 46 43 0.02 8.0 1:400 0 0 0.02 1.6 1:80 16 1 0.004 200.0 1:50000 100 100 0.004 40.0 1:10000 60 55 0.004 8.0 1:2000 4 21 0.004 1.6 1:400 41 21 0.0008 200.0 1:250000 100 100 0.0008 40.0 1:50000 46 43 0.0008 8.0 1:10000 37 0 0.0008 1.6 1:2000 0 1 0.02 200.0 1:10000 26 17 0.02 40.0 1:2000 49 35 0.02 8.0 1:400 29 25 0.02 1.6 1:80 16 0

TABLE C11 in vitro—Test with Cercospora beticola (1.002) (13.001) (2.005) (15.043) (2.002) difeno- (5.010) flu- fluo- fluoxa- Colby (I-339) bixafen conazole dithianon dioxonil pyram piprolin Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 98 0.2 61 0.04 0 0.008 28 1 0 1 99 0.2 98 0.04 60 0.008 5 2 100 0.4 3 0.08 0 5 93 20 56 4 0 0.8 31 0.16 28 20 0 1 1 1:1 100 98 1 1 1:5 74 61 1 1 1:25 25 0 0.2 1 1:5 100 99 0.2 0.2 1:1 100 98 0.2 0.04 1:0.2 88 60 0.2 0.008 1:0.04 18 5 0.2 2 1:10 100 100 0.2 0.4 1:2 39 3 0.2 0.08 1:0.4 5 0 0.008 2 1:250 100 100 0.008 0.4 1:50 15 3 0.008 0.08 1:10 17 0 1 5 1:5 100 100 0.2 5 1:25 97 93 0.04 5 1:125 99 93 0.008 5 1:625 98 93 0.2 20 1:100 60 60 0.2 4 1:20 47 9 0.2 0.8 1:4 68 38 0.2 0.16 1:0.8 36 35 1 20 1:20 100 100 0.2 20 1:100 38 9 0.04 20 1:500 3 3

TABLE C12 in vitro—Test with Cercospora beticola (1.055) (3.012) (2.028) (2.038) mefen- fluoxa- (5.012) inpyr- isoflucy- (6.002) triflu- Colby (I-339) strobin folpet fluxam pram isotianil conazole Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 98 0.2 61 0.04 0 0.008 28 0.4 100 0.016 54 1 100 0.008 7 1 25 0.2 23 0.04 22 1 44 0.2 16 0.04 14 0.008 8 20 3 4 8 0.04 84 0.008 24 0.04 0.4 1:10 100 100 0.04 0.016 1:0.4 72 55 0.008 0.4 1:50 100 100 0.008 0.016 1:2 64 62 0.2 1 1:5 100 100 0.2 0.008 1:0.04 55 7 0.04 1 1:25 93 100 0.04 0.008 1:0.2 10 7 0.2 1 1:5 50 25 0.2 0.2 1:1 57 23 0.2 0.04 1:0.2 60 22 0.2 1 1:5 70 44 0.2 0.2 1:1 64 16 0.2 0.04 1:0.2 26 14 0.2 0.008 1:0.04 93 8 0.04 1 1:25 67 44 0.04 0.2 1:5 34 16 0.04 0.04 1:1 46 14 0.04 0.008 1:0.2 12 8 0.2 20 1:100 39 22 0.2 4 1:20 50 26 0.008 20 1:2500 0 3 0.008 4 1:500 17 8 0.2 0.04 1:0.2 89 87 0.2 0.008 1:0.04 56 39 0.008 0.04 1:1 86 86 0.008 0.008 1:0.2 54 33

TABLE C13 in vitro—Test with Cercospora beticola (17.012) (12.004) (15.016) Paeni- (13.004) (1.018) (7.005) meta- metra- bacillus pro- prothio- pyri- Colby (I-339) laxyl-m fenone terrae quinazid conazole methanil Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 98 0.2 61 0.04 0 0.008 28 20 0 4 10 5 10 1 0 0.2 0 200 100 40 81 8 0 10 0 2 0 0.5 100 0.1 100 0.004 39 0.8 0 0.2 20 1:100 37 20 0.2 4 1:20 35 28 0.008 20 1:2500 4 0 0.008 4 1:500 12 10 0.04 5 1:125 44 10 0.04 1 1:25 14 0 0.04 0.2 1:5 0 0 0.04 200 1:5000 100 100 0.04 40 1:1000 86 81 0.04 8 1:200 0 0 0.04 10 1:250 30 3 0.04 2 1:50 0 3 0.008 10 1:1250 28 0 0.008 2 1:250 0 0 0.008 0.5 1:62.5 100 100 0.008 0.1 1:12.5 100 100 0.008 0.004 1:0.5 49 39 0.2 0.8 1:4 88 83 0.04 0.8 1:20 66 3 0.008 0.8 1:100 64 0

TABLE C14 in vitro—Test with Cercospora beticola (1.021) (1.002) (3.025) tebu- (5.003) difeno- fenpicox- Colby (I-339) conazole (I-338) (1.067) captan conazole amid Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 98 0.2 61 0.04 0 0.008 28 0.2 62 0.04 1 0.008 4 1 17 0.2 7 0.04 0 0.008 0 2 100 0.4 68 0.08 0 5 100 1 61 0.04 0 0.04 51 0.008 16 1 97 0.2 17 0.2 0.2 1:1 98 79 0.2 0.04 1:0.2 62 45 0.2 0.008 1:0.04 64 47 0.04 0.2 1:5 94 70 0.04 0.04 1:1 57 21 0.04 0.008 1:0.2 20 23 0.008 0.2 1:25 83 62 0.008 0.04 1:5 37 1 0.008 0.008 1:1 15 4 1 2 1:2 100 100 1 0.4 1:0.4 80 74 1 0.08 1:0.08 42 17 0.2 2 1:10 100 100 0.2 0.4 1:2 99 70 0.2 0.08 1:0.4 7 7 0.04 2 1:50 100 100 0.04 0.4 1:10 97 68 0.04 0.08 1:2 0 0 0.008 2 1:250 100 100 0.008 0.4 1:50 100 68 0.008 0.08 1:10 31 0 0.2 5 1:25 100 100 0.2 1 1:5 76 64 0.2 0.04 1:0.2 0 7 0.008 5 1:625 100 100 0.008 1 1:125 69 61 0.008 0.04 1:5 44 0 1 0.04 1:0.04 100 51 1 0.008 1:0.008 23 16 0.2 0.008 1:0.04 40 18 0.008 0.008 1:1 19 16 1 1 1:1 100 97 1 0.2 1:0.2 36 17 0.2 1 1:5 100 97 0.2 0.2 1:1 45 19 0.008 1 1:125 100 97 0.008 0.2 1:25 34 17

TABLE C15 in vitro—Test with Cercospora beticola (2.005) (15.043) (3.012) (1.062) (2.028) fluo- fluoxa- fluoxa- fluoxytio- (5.012) inpyr- Colby (I-338) pyram piprolin strobin conazole folpet fluxam Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 27 0.2 15 0.04 11 0.008 0 20 7 0.8 11 20 0 4 3 0.8 0 0.16 12 0.4 100 0.08 96 0.016 19 1 48 0.2 0 0.04 0 1 86 0.008 2 1 0.8 1:0.8 41 36 0.04 20 1:500 54 17 0.008 20 1:2500 9 7 0.008 0.8 1:100 13 11 0.04 20 1:500 13 11 0.04 4 1:100 15 14 0.008 20 1:2500 0 0 0.008 4 1:500 11 3 0.008 0.8 1:100 13 0 0.008 0.16 1:20 20 12 1 0.4 1:0.4 100 100 1 0.08 1:0.08 99 97 1 0.016 1:0.016 70 41 0.008 1 1:125 58 48 0.008 0.2 1:25 34 0 0.008 0.04 1:5 0 0 1 1 1:1 100 89 0.2 1 1:5 100 86 0.04 1 1:25 100 86 0.008 1 1:125 100 86 0.2 0.008 1:0.04 9 2 0.04 0.008 1:0.2 15 2 0.008 0.008 1:1 17 2

TABLE C16 in vitro—Test with Cercospora beticola (3.030) (2.038) (5.013) (12.004) (15.016) metyl- isoflucy- (6.002) manco- metalaxyl- metra- tetra- Colby (I-338) pram isotianil zeb m fenone prole Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 27 0.2 15 0.04 11 0.008 0 1 40 0.2 34 0.04 14 0.008 40 100 0 0.8 0 100 18 5 1 0.04 2 0.04 100 0.008 37 1 0.04 1:0.04 42 32 1 0.008 1:0.008 55 52 0.2 0.04 1:0.2 42 14 0.2 0.008 1:0.04 42 40 0.008 1 1:125 54 40 0.008 0.2 1:25 38 34 0.008 0.04 1:5 32 14 1 100 1:100 24 8 0.2 100 1:500 26 0 0.008 100 1:12500 0 0 1 0.8 1:0.8 10 8 1 100 1:100 41 25 0.2 100 1:500 49 18 0.04 100 1:2500 25 23 0.2 5 1:25 14 3 0.2 0.04 1:0.2 12 3 0.04 5 1:125 12 1 0.04 0.04 1:1 11 2 0.2 0.04 1:0.2 100 100 0.2 0.008 1:0.04 44 39 0.04 0.04 1:1 100 100 0.04 0.008 1:0.2 55 39 0.008 0.04 1:5 100 100 0.008 0.008 1:1 69 42

TABLE C17 in vitro—Test with Cercospora beticola (2.017) (1.018) (7.005) (13.005) (1.020) pen- (5.018) prothio- pyrmetha- quinoxi- spirox- Colby (I-338) flufen propineb conazole nil fen amin Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 27 0.2 15 0.04 11 0.008 0 1 0 4 0 0.5 0 0.1 15 0.02 0 0.004 30 0.16 0 2 0 0.08 3 4 6 0.8 4 0.16 0 1 1 1:1 38 19 0.2 1 1:5 20 2 0.04 1 1:25 10 0 1 4 1:4 29 0 0.2 4 1:20 20 0 0.04 4 1:100 31 0 0.008 4 1:500 7 0 1 0.5 1:0.5 16 0 1 0.1 1:0.1 28 15 1 0.02 1:0.02 24 0 0.2 0.5 1:2.5 16 0 0.2 0.1 1:0.5 27 15 0.2 0.02 1:0.1 30 0 0.2 0.004 1:0.02 45 30 1 0.16 1:0.16 43 0 0.2 0.16 1:0.8 8 0 0.04 0.16 1:4 13 0 0.008 0.16 1:20 0 0 0.2 2 1:10 21 8 0.2 0.08 1:0.4 10 11 0.04 2 1:50 0 0 0.04 0.08 1:2 19 3 0.008 2 1:250 10 0 0.008 0.08 1:10 13 3 1 4 1:4 37 17 1 0.8 1:0.8 17 15 1 0.16 1:0.16 22 11

TABLE C18 in vitro—Test with Cercospora beticola (1.002) (3.025) (3.020) difeno- fen- trifloxy- (2.002) (5.003) cona- picoxa- Colby (I-338) strobin (I-130) (17.001) bixafen captan zole mid Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 11 0.2 8 0.04 0 0.008 0 0.008 96 1 96 0.2 5 0.04 0 0.008 0 8 0 1.6 1 1 20 0.2 14 5 100 1 38 0.4 0 0.2 100 0.04 62 0.008 11 1 100 0.2 31 0.008 0 1 0.008 1:0.008 98 96 0.2 0.008 1:0.04 99 96 0.04 0.008 1:0.2 100 96 0.04 8 1:8 99 96 0.04 1.6 1:1.6 100 96 0.008 8 1:1000 11 0 0.008 1.6 1:200 3 1 1 1 1:1 100 97 1 0.2 1:0.2 100 97 0.008 1 1:125 28 20 0.008 0.2 1:25 30 14 0.04 5 1:125 100 100 0.04 1 1:25 74 38 0.04 0.4 1:5 0 0 0.008 5 1:625 100 100 0.008 1 1:125 74 38 0.008 0.4 1:25 3 0 0.04 0.2 1:5 100 100 0.04 0.04 1:1 86 62 0.2 0.008 1:0.04 24 11 0.2 1 1:5 100 100 0.2 0.2 1:1 82 31 0.2 0.008 1:0.04 14 0 0.04 1 1:25 100 100 0.04 0.2 1:5 63 31 0.04 0.008 1:0.2 0 0 0.008 1 1:125 100 100 0.008 0.2 1:25 35 31 0.008 0.008 1:1 4 0

TABLE C19 in vitro—Test with Cercospora beticola (1.062) (1.055) (2.005) (15.043) fluoxy- (2.028) (2.038) mefen- fluo- fluoxa- tiocona- (5.012) inpyr- isoflucy- triflu- Effi- Colby (I-130) pyram piprolin zole folpet fluxam pram conazole cacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 100 0.2 4 0.04 0 0.008 0 20 12 4 0 0.8 7 20 0 4 0 0.8 0 1 54 0.008 0 0.2 16 0.04 0 1 5 0.2 6 0.04 0 1 35 0.2 5 0.04 13 0.008 0 0.04 93 0.008 14 1 4 1:4 100 100 0.2 4 1:20 20 15 0.04 4 1:100 14 4 0.008 20 1:2500 40 12 0.008 4 1:500 0 0 0.008 0.8 1:100 15 7 0.008 20 1:2500 19 0 0.008 4 1:500 0 0 0.008 0.8 1:100 10 0 0.008 1 1:125 70 54 0.008 0.008 1:1 0 0 0.2 0.2 1:1 42 16 0.2 0.04 1:0.2 0 0 0.04 0.2 1:5 41 16 0.04 0.04 1:1 15 0 0.2 1 1:5 58 5 0.2 0.2 1:1 46 6 0.2 0.04 1:0.2 57 0 0.04 1 1:25 42 5 0.04 0.2 1:5 39 6 0.04 0.04 1:1 0 0 0.008 1 1:125 32 13 0.008 0.2 1:25 26 14 0.008 0.04 1:5 26 8 1 1 1:1 100 99 1 0.2 1:0.2 99 99 1 0.04 1:0.04 100 99 1 0.008 1:0.008 100 99 0.2 1 1:5 45 35 0.2 0.2 1:1 51 5 0.2 0.04 1:0.2 38 13 0.2 0.008 1:0.04 26 0 0.04 1 1:25 51 35 0.04 0.2 1:5 16 5 0.04 0.04 1:1 25 13 0.04 0.008 1:0.2 1 0 0.2 0.04 1:0.2 99 93 0.2 0.008 1:0.04 73 14 0.008 0.04 1:5 99 93 0.008 0.008 1:1 13 14

TABLE C20 in vitro—Test with Cercospora beticola (3.030) (12.004) (15.016) metyl- (13.004) (13.005) (1.020) meta- metra- tetra- (5.018) pro- quinoxy- spirox- Effi- Colby (I-130) laxyl-m fenone prole propineb quinazid fen amin cacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 100 0.2 4 0.04 0 0.008 0 100 0 20 0 0.2 0 0.04 0 0.2 100 0.008 0 4 92 0.08 0 10 4 2 0 0.4 0 0.8 0 0.16 0 0.04 100 1:2500 21 0 0.04 20 1:500 0 0 0.008 100 1:12500 20 0 0.008 20 1:2500 0 0 0.04 0.2 1:5 19 0 0.04 0.04 1:1 14 0 0.008 0.2 1:25 14 0 0.008 0.04 1:5 0 0 0.04 0.2 1:5 100 100 0.04 0.008 1:0.2 48 0 0.008 0.2 1:25 100 100 0.008 0.008 1:1 3 0 0.2 4 1:20 100 92 0.04 4 1:100 100 92 0.008 4 1:500 100 92 0.2 0.08 1:0.4 41 0 0.04 0.08 1:2 53 0 0.008 0.08 1:10 25 0 0.2 10 1:50 16 4 0.2 2 1:10 9 0 0.2 0.4 1:2 2 0 0.008 10 1:1250 21 4 0.2 0.8 1:4 18 0 0.2 0.16 1:0.8 0 0 0.008 0.8 1:100 7 0 0.008 0.16 1:20 6 0

TABLE D1 in vitro—Test with Colletotrichum lindemuthianum (1.055) (2.005) (3.020) mefen- (1.021) (1.020) (2.002) fluo- trifloxy- triflu- tebu- spiro- Colby (I-052) bixafen pyram strobin conazole conazole xamine Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 100 0.02 100 0.004 0 0.0008 0 1.0 16 0.2 0 0.04 0 0.008 6 20.0 23 4.0 3 0.8 6 0.16 11 1.0 84 0.2 85 0.04 66 0.2 11 0.04 0 0.008 7 1.0 4 0.2 0 0.04 13 0.008 0 20.0 0 4.0 8 0.8 0 0.16 0 0.0008 1.0 1:1250  13 20 0.0008 0.2 1:250   29 5 0.0008 0.04 1:50    11 5 0.0008 0.008 1:10    20 10 0.0008 20.0 1:25000 55 26 0.0008 4.0 1:5000  29 7 0.0008 0.8 1:1000  14 10 0.0008 0.16 1:200   12 15 0.1 1.0 1:10    99 100 0.1 0.2 1:2     99 100 0.1 0.04 1:0.4    99 100 0.004 1.0 1:250   92 86 0.004 0.2 1:50    87 88 0.004 0.04 1:10    77 72 0.0008 1.0 1:1250  90 84 0.0008 0.2 1:250   89 85 0.0008 0.04 1:50    75 66 0.1 0.2 1:2     99 100 0.1 0.04 1:0.4    98 100 0.1 0.008 1:0.08   100 100 0.004 0.2 1:50    61 11 0.004 0.04 1:10    25 0 0.004 0.008 1:2     22 7 0.0008 0.2 1:250   24 11 0.0008 0.04 1:50    0 0 0.0008 0.008 1:10    24 7 0.1 1.0 1:10    98 100 0.1 0.2 1:2     98 100 0.1 0.04 1:0.4    99 100 0.1 0.008 1:0.08   99 100 0.004 1.0 1:250   22 4 0.004 0.2 1:50    39 0 0.004 0.04 1:10    19 13 0.004 0.008 1:2     20 0 0.1 20.0 1:1000  100 100 0.1 4.0 1:200   99 100 0.1 0.8 1:40    100 100 0.1 0.16 1:8     100 100 0.02 20.0 1:5000  33 0 0.02 4.0 1:1000  19 8 0.02 0.8 1:200   19 0 0.02 0.16 1:40    19 0

TABLE D2 in vitro—Test with Colletotrichum lindemuthianum (15.012) (17.012) (13.001) (13.004) (5.010) fosetyl- Paeni- Colby fludio- proquin dithia- alumi- bacillus (18.001) Effi- expected (I-052) xonil azid non nium terrae FLiPPER cacy value (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % % 0.1 100 0.02 100 0.004 0 0.0008 0 5.0 88 0.2 58 0.04 0 10.0 25 2.0 2 0.4 0 0.08 0 20.0 100 0.8 0 0.16 0 100.0 39 20.0 0 200.0 99 40.0 7 8.0 0 1.6 0 200.0 0 40.0 2 8.00 0 0.1 5.0 1:50     99 100 0.1 0.2 1:2      96 100 0.1 0.04 1:0.4     100 100 0.004 5.0 1:1250   87 88 0.004 0.2 1:50     85 58 0.004 0.04 1:10     5 0 0.0008 5.0 1:6250   89 88 0.0008 0.2 1:250    54 58 0.0008 0.04 1:50     18 0 0.1 10.0 1:100    96 100 0.1 2.0 1:20     97 100 0.1 0.4 1:4      99 100 0.1 0.08 1:0.8     97 100 0.004 10.0 1:2500   26 25 0.004 2.0 1:500    13 2 0.004 0.4 1:100    22 0 0.004 0.08 1:20     36 0 0.0008 10.0 1:12500  36 25 0.0008 2.0 1:2500   24 2 0.0008 0.4 1:500    0 0 0.0008 0.08 1:100    0 0 0.1 20.0 1:200    99 100 0.1 0.8 1:8      97 100 0.1 0.16 1:1.6     100 100 0.004 20.0 1:5000   100 100 0.004 0.8 1:200    20 15 0.004 0.16 1:40     24 15 0.1 100.0 1:1000   99 100 0.1 20.0 1:200    95 100 0.004 100.0 1:25000  83 48 0.004 20.0 1:5000   20 15 0.0008 100.0 1:125000 63 49 0.0008 20.0 1:25000  17 16 0.0008 200.0 1:250000 100 99 0.0008 40.0 1:50000  39 7 0.0008 8.0 1:10000  2 0 0.0008 1.6 1:2000   19 0 0.1 200.0 1:2000   98 100 0.1 40.0 1:400    98 100 0.1 8.00 1:80     96 100 0.004 200.0 1:50000  44 20 0.004 40.0 1:10000  28 21 0.004 8.00 1:2000   13 20 0.0008 200.0 1:250000 15 0 0.0008 40.0 1:50000  10 2 0.0008 8.00 1:10000  0 0

TABLE D3 in vitro-Test with Colletotrichum lindemuthianum (1.055) (3.025) (3.020) mefen- (13.005) Colby (2.002) fenpico- trifloxys- triflu- quino- (5.003) Effi- expected (I-300) bixafen xamid trobin conazole xyfen captan cacy value (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % % 0.1 100 0.02 11 0.004 0 0.0008 0 1.0 5 0.2 0 0.04 0 0.008 0 5.0 79 1.0 69 0.2 77 0.04 59 0.008 25 1.0 0 0.04 3 0.008 0 10.0 24 2.0 0 0.4 0 0.08 1 20.0 100 4.0 100 0.8 0 0.16 9 0.1 1.0 1:10    98 100 0.1 0.2 1:2     100 100 0.1 0.04 1:0.4   100 100 0.1 0.008 1:0.08  92 100 0.02 1.0 1:50    18 5 0.02 0.2 1:10    10 0 0.02 0.04 1:2     22 0 0.02 0.008 1:0.4   11 0 0.1 5.0 1:50    100 100 0.1 1.0 1:10    100 100 0.02 5.0 1:250   84 83 0.02 1.0 1:50    78 74 0.004 5.0 1:1250  83 81 0.004 1.0 1:250   75 72 0.0008 5.0 1:6250  87 79 0.0008 1.0 1:1250  70 70 0.02 0.2 1:10    76 81 0.02 0.04 1:2     76 66 0.02 0.008 1:0.4   49 38 0.004 0.2 1:50    86 81 0.004 0.04 1:10    82 67 0.004 0.008 1:2     33 39 0.0008 0.2 1:250   82 78 0.0008 0.04 1:50    67 60 0.0008 0.008 1:10    38 27 0.1 1.0 1:10    99 100 0.1 0.04 1:0.4   100 100 0.1 0.008 1:0.08  100 100 0.02 1.0 1:50    12 12 0.02 0.04 1:2     13 14 0.02 0.008 1:0.4   29 12 0.004 1.0 1:250   19 3 0.004 0.04 1:10    0 5 0.004 0.008 1:2     8 3 0.0008 1.0 1:1250  49 5 0.0008 0.04 1:50    0 8 0.0008 0.008 1:10    15 5 0.1 10.0 1:100   100 92 0.1 2.0 1:20    100 89 0.1 0.4 1:4     100 89 0.1 0.08 1:0.8   100 89 0.02 10.0 1:500   36 33 0.02 2.0 1:100   23 13 0.02 0.4 1:20    12 13 0.02 0.08 1:4     29 13 0.1 20.0 1:200   100 100 0.1 4.0 1:40    100 100 0.1 0.8 1:8     100 89 0.1 0.16 1:1.6   97 90

TABLE D4 in vitro-Test with Colletotrichum lindemuthianum (15.012) (5.010) (5.013) (5.018) fosetyl- (17.001) Colby dithia- (5.012) man- pro- alumi- Bacillus Effi- expected (I-300) non folpet cozeb pineb nium subtilis cacy value (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % % 0.1 100 0.02 11 0.004 0 0.0008 0 20.0 99 4.0 100 0.8 0 0.16 1 10.0 100 2.0 98 0.4 13 0.08 0 10.0 100 0.4 0 0.08 4 100.0 94 20.0 100 4.0 32 0.8 5 100.0 58 20.0 22 4.0 0 0.8 0 200.0 0 40.0 5 1.6 0 0.1 20.0 1:200   100 100 0.1 4.0 1:40    97 100 0.1 0.8 1:8     89 89 0.1 0.16  1:1.6    100 89 0.1 10.0 1:100   99 100 0.1 2.0 1:20    99 100 0.1 0.4 1:4     95 91 0.1 0.08  1:0.8    94 89 0.02 10.0 1:500   100 100 0.02 0.4 1:20    21 11 0.02 0.08 1:4     13 14 0.004 10.0 1:2500  100 100 0.004 0.4 1:100   0 0 0.004 0.08 1:20    0 4 0.0008 10.0 1:12500 100 100 0.0008 0.4 1:500   0 0 0.0008 0.08 1:100   11 4 0.02 100.0 1:5000  100 95 0.02 20.0 1:1000  100 100 0.02 4.0 1:200   69 39 0.02 0.8 1:40    18 15 0.004 100.0 1:25000 69 58 0.004 20.0 1:5000  20 22 0.004 4.0 1:1000  0 0 0.004 0.8 1:200   0 0 0.1 200.0 1:2000  100 99 0.1 40.0 1:400   99 99 0.1 1.6 1:16    99 99 0.02 200.0 1:10000 70 9 0.02 40.0 1:2000  11 13 0.02 1.6 1:80    18 9 0.004 200.0 1:50000 31 0 0.004 40.0 1:10000 0 5 0.004 1.6 1:400   18 0

TABLE D5 in vitro-Test with Colletotrichum lindemuthianum (7.005) (2.002) (2.005) (2.028) (2.038) (3.025) pyrime- bixafen fluo- inpyr- isoflu- fenpi- Effi- Colby (I-302) thanil (ppm) pyram fluxam cypram coxamid cacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 100 0.02 12 0.004 0 0.0008 1 20.0 16 4.0 0 0.8 1 0.16 0 1.0 9 0.2 0 0.04 0 0.008 0 20.0 28 4.0 34 0.8 0 0.16 0 1.0 14 0.2 1 0.04 0 0.008 0 1.0 18 0.2 0 0.04 14 0.008 0 5.0 86 1.0 66 0.2 5 0.04 0 0.02 20.0 1:1000 30 16 0.02 4.0 1:200  29 0 0.02 0.8 1:40   30 1 0.02 0.16 1:8    39 0 0.1 1.0 1:10   98 100 0.1 0.2 1:2    100 100 0.1 0.04  1:0.4   100 100 0.1 0.008 1:0.08  100 100 0.02 1.0 1:50   11 9 0.02 0.2 1:10   15 0 0.02 0.04 1:2    40 0 0.02 0.008  1:0.4   33 0 0.0008 1.0 1:1250 20 9 0.0008 0.2 1:250  0 0 0.0008 0.04 1:50   0 0 0.0008 0.008 1:10   0 0 0.1 20.0 1:200  98 100 0.1 4.0 1:40   100 100 0.1 0.8 1:8    100 100 0.1 0.16  1:1.6   97 100 0.02 20.0 1:1000 62 28 0.02 4.0 1:200  25 34 0.02 0.8 1:40   32 0 0.02 0.16 1:8    32 0 0.1 1.0 1:10   95 100 0.1 0.2 1:2    100 100 0.1 0.04  1:0.4   100 100 0.1 0.008  1:0.08  97 100 0.02 1.0 1:50   21 14 0.02 0.2 1:10   59 1 0.02 0.04 1:2    31 0 0.02 0.008  1:0.4   33 0 0.1 1.0 1:10   99 100 0.1 0.2 1:2    100 100 0.1 0.04  1:0.4   100 100 0.1 0.008  1:0.08  100 100 0.02 1.0 1:50   33 28 0.02 0.2 1:10   22 12 0.02 0.04 1:2    16 24 0.02 0.008  1:0.4   34 12 0.1 5.0 1:50   97 100 0.1 1.0 1:10   98 100 0.1 0.2 1:2    100 100 0.1 0.04  1:0.4   100 100 0.02 5.0 1:250  91 87 0.02 1.0 1:50   79 70 0.02 0.2 1:10   32 16 0.02 0.04 1:2    58 12 0.004 5.0 1:1250 84 86 0.004 1.0 1:250  72 66 0.004 0.2 1:50   25 5 0.004 0.04 1:10   6 0 0.0008 5.0 1:6250 88 86 0.0008 1.0 1:1250 66 66 0.0008 0.2 1:250  24 6 0.0008 0.04 1:50   0 1

TABLE D6 in vitro-Test with Colletotrichum lindemuthianum (1.002) (1.055) (3.020) difeno- mefen- (1.018) (1.021) (1.020) Colby trifloxy- cona- triflu- prothio- tebu- spiro- Effi- expected (I-302) strobin zole conazole conazole conazole xamine cacy value (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % % 0.1 100 0.02 12 0.004 0 0.0008 1 1.0 88 0.2 92 0.04 80 0.008 30 1.0 16 0.2 0 0.04 2 0.008 0 1.0 13 0.2 6 0.04 0 0.008 0 1.0 100 0.2 100 0.04 20 0.008 0 1.0 35 0.2 17 0.04 0 0.008 32 20.0 6 0.8 0 0.16 13 0.1 1.0 1:10   96 100 0.1 0.2 1:2    100 100 0.1 0.04  1:0.4   100 100 0.1 0.008  1:0.08  97 100 0.02 1.0 1:50   100 90 0.02 0.2 1:10   95 93 0.02 0.04 1:2    83 82 0.02 0.008  1:0.4   53 38 0.004 1.0 1:250  97 88 0.004 0.2 1:50   90 92 0.004 0.04 1:10   77 80 0.004 0.008 1:2    41 30 0.0008 1.0 1:1250 95 89 0.0008 0.2 1:250  99 92 0.0008 0.04 1:50   84 80 0.0008 0.008 1:10   42 30 0.1 1.0 1:10   97 100 0.1 0.2 1:2    96 100 0.1 0.04  1:0.4   94 100 0.1 0.008  1:0.08  96 100 0.02 1.0 1:50   59 25 0.02 0.2 1:10   40 12 0.02 0.04 1:2    16 13 0.02 0.008  1:0.4   61 12 0.004 1.0 1:250  7 16 0.004 0.2 1:50   17 0 0.004 0.04 1:10   26 2 0.004 0.008 1:2    6 0 0.1 1.0 1:10   100 98 0.1 0.2 1:2    100 98 0.1 0.04  1:0.4   100 98 0.1 0.008  1:0.08  100 98 0.02 1.0 1:50   46 16 0.02 0.2 1:10   32 10 0.02 0.04 1:2    17 4 0.02 0.008  1:0.4   46 4 0.1 1.0 1:10   100 100 0.1 0.2 1:2    100 100 0.1 0.04  1:0.4   100 98 0.1 0.008  1:0.08  98 98 0.02 1.0 1:50   100 100 0.02 0.2 1:10   100 100 0.02 0.04 1:2    41 22 0.02 0.008  1:0.4   24 4 0.1 1.0 1:10   98 99 0.1 0.2 1:2    96 98 0.1 0.04  1:0.4   99 98 0.1 0.008  1:0.08  99 99 0.02 1.0 1:50   66 37 0.02 0.2 1:10   52 20 0.02 0.04 1:2    44 4 0.02 0.008  1:0.4   31 35 0.1 20.0 1:200  100 100 0.1 0.8 1:8    100 100 0.1 0.16  1:1.6   99 100 0.02 20.0 1:1000 18 22 0.02 0.8 1:40   28 17 0.02 0.16 1:8    30 27

TABLE D7 in vitro-Test with Colletotrichum lindemuthianum (13.001) (13.005) (5.018) fludio- quino- (5.003) (5.012) pro- Effi- Colby (I-302) (15.064) xonil xyfen captan folpet pineb cacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 100 0.02 12 0.004 0 0.0008 1 2.0 0 0.4 0 0.08 16 5.0 90 1.0 85 0.2 60 0.04 11 2.0 0 0.4 0 0.08 0 20.0 100 4.0 100 0.8 3 0.16 0 10.0 100 2.0 100 0.4 0 0.08 0 100.0 100 20.0 100 4.0 50 0.1 2.0 1:20    100 100 0.1 0.4 1:4     98 100 0.1 0.08  1:0.8    98 100 0.02 2.0 1:100   29 17 0.02 0.4 1:20    30 17 0.02 0.08 1:4     48 30 0.02 5.0 1:250   96 92 0.02 1.0 1:50    99 88 0.02 0.2 1:10    83 67 0.02 0.04 1:2     40 26 0.004 5.0 1:1250  95 91 0.004 1.0 1:250   100 87 0.004 0.2 1:50    78 65 0.004 0.04 1:10    53 22 0.0008 5.0 1:6250  92 91 0.0008 1.0 1:1250  89 87 0.0008 0.2 1:250   79 65 0.0008 0.04 1:50    24 22 0.1 2.0 1:20    100 100 0.1 0.4 1:4     99 100 0.1 0.08  1:0.8    100 100 0.02 2.0 1:100   22 15 0.02 0.4 1:20    26 15 0.02 0.08 1:4     36 15 0.004 2.0 1:500   0 0 0.004 0.4 1:100   16 0 0.004 0.08 1:20    9 0 0.1 20.0 1:200   100 100 0.1 4.0 1:40    100 100 0.1 0.8 1:8     100 100 0.1 0.16  1:1.6    98 100 0.02 20.0 1:1000  100 100 0.02 4.0 1:200   100 100 0.02 0.8 1:40    23 18 0.02 0.16 1:8     33 15 0.1 10.0 1:100   100 100 0.1 2.0 1:20    100 100 0.1 0.4 1:4     97 100 0.1 0.08  1:0.8    95 100 0.02 10.0 1:500   100 100 0.02 2.0 1:100   100 100 0.02 0.4 1:20    24 15 0.02 0.08 1:4     47 15 0.02 100.0 1:5000  100 100 0.02 20.0 1:1000  100 100 0.02 4.0 1:200   100 64 0.004 100.0 1:25000 100 100 0.004 20.0 1:5000  100 100 0.004 4.0 1:1000  69 54

TABLE D8 in vitro-Test with Colletotrichum lindemuthianum (15.012) (17.012) fosetyl- (15.016) (6.002) (17.001) Paeni- alumi- metra- iso- Bacillus bacillus (18.001) Effi- Colby (I-302) nium fenone tianil subtilis terrae FLiPPER cacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 100 0.02 12 0.004 0 0.0008 1 100.0 70 20.0 8 4.0 0 20.0 21 4.0 12 0.8 10 100.0 0 20.0 3 4.0 9 0.8 0 200.0 0 40.0 0 8.0 0 1.6 0 200.0 100 40.0 24 8.0 0 1.6 2 200.0 0 40.0 0 8.0 12 1.6 6 0.1 100.0 1:1000  96 100 0.1 20.0 1:200   95 100 0.1 4.0 1:40    96 100 0.02 100.0 1:5000  79 76 0.02 20.0 1:1000  50 34 0.02 4.0 1:200   31 29 0.1 20.0 1:200   99 100 0.1 4.0 1:40    99 100 0.1 0.8 1:8     95 100 0.02 20.0 1:1000  60 43 0.02 4.0 1:200   29 37 0.02 0.8 1:40    63 36 0.1 100.0 1:1000  99 100 0.1 20.0 1:200   100 100 0.1 4.0 1:40    100 100 0.1 0.8 1:8     100 100 0.02 100.0 1:5000  16 0 0.02 20.0 1:1000  9 3 0.02 4.0 1:200   16 9 0.02 0.8 1:40    21 0 0.1 200.0 1:2000  100 100 0.1 40.0 1:400   100 100 0.1 8.0 1:80    100 100 0.1 1.6 1:16    100 100 0.02 200.0 1:10000 64 0 0.02 40.0 1:2000  6 0 0.02 8.0 1:400   49 0 0.02 1.6 1:80    23 0 0.02 200.0 1:10000 100 100 0.02 40.0 1:2000  51 24 0.02 8.0 1:400   5 0 0.02 1.6 1:80    15 2 0.004 200.0 1:50000 100 100 0.004 40.0 1:10000 24 16 0.004 8.0 1:2000  0 0 0.004 1.6 1:400   0 2 0.02 200.0 1:10000 96 0 0.02 40.0 1:2000  12 0 0.02 8.0 1:400   25 12 0.02 1.6 1:80    8 6 0.004 200.0 1:50000 14 0 0.004 40.0 1:10000 0 0 0.004 8.0 1:2000  15 12 0.004 1.6 1:400   17 6

TABLE E1 in vitro-Test with Cordana musae (1.021) (7.005) (2.038) (3.020) tebu- (1.020) pyrime- isoflu- trifloxy- cona- spiro- Effi- Colby (I-052) thanil cypram strobin zole xamine (15.064) cacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 100 0.02 83 0.004 0 0.0008 0 20.0 4 4.0 24 1.0 0 0.2 0 0.04 0 0.008 0 1.0 66 0.008 3 1.0 99 0.2 29 0.04 0 0.008 0 20.0 9 4.0 0 0.8 0 10.0 27 2.0 0 0.4 0 0.08 0 0.02 20.0 1:1000  100 83 0.02 4.0 1:200   99 86 0.004 20.0 1:5000  19 4 0.004 4.0 1:1000  36 24 0.0008 20.0 1:25000 53 4 0.0008 4.0 1:5000  17 24 0.02 1.0 1:50    100 83 0.02 0.2 1:10    99 83 0.02 0.04 1:2     100 83 0.02 0.008  1:0.4    83 83 0.1 1.0 1:10    100 100 0.1 0.008  1:0.08   99 100 0.004 1.0 1:250   72 66 0.004 0.008 1:2     54 3 0.0008 1.0 1:1250  73 66 0.0008 0.008 1:10    29 3 0.1 1.0 1:10    100 100 0.1 0.2 1:2     100 100 0.1 0.04  1:0.4    99 100 0.1 0.008  1:0.08   100 100 0.02 1.0 1:50    98 100 0.02 0.2 1:10    87 82 0.02 0.04 1:2     74 75 0.02 0.008  1:0.4    81 75 0.004 1.0 1:250   100 99 0.004 0.2 1:50    57 29 0.004 0.04 1:10    0 0 0.004 0.008 1:2     0 0 0.0008 1.0 1:1250  99 99 0.0008 0.2 1:250   56 29 0.0008 0.04 1:50    0 0 0.0008 0.008 1:10    0 0 0.1 20.0 1:200   100 100 0.1 4.0 1:40    100 100 0.1 0.8 1:8     100 100 0.02 20.0 1:1000  100 78 0.02 4.0 1:200   70 76 0.02 0.8 1:40    82 76 0.004 20.0 1:5000  37 38 0.004 4.0 1:1000  36 32 0.004 0.8 1:200   36 32 0.02 10.0 1:500   97 83 0.02 2.0 1:100   77 76 0.02 0.4 1:20    84 76 0.02 0.08 1:4     80 76

TABLE E2 in vitro-Test with Cordana musae (13.004) (17.012) (13.001) pro- (13.005) (5.018) Paeni- fludio- quina- quino- (5.003) pro- bacillus Effi- Colby (I-052) xonil zid xyfen captan pineb terrae cacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 100 0.02 83 0.004 0 0.0008 0 5.0 55 1.0 83 0.2 0 0.04 2 10.0 26 2.0 1 0.4 0 0.08 0 10.0 0 2.0 0 0.4 0 4.0 0 0.16 15 100.0 100 20.0 43 4.0 11 0.8 1 200.0 100 40.0 23 8.0 28 1.6 0 0.02 5.0 1:250   100 89 0.02 1.0 1:50    99 96 0.02 0.2 1:10    76 76 0.02 0.04 1:2     85 77 0.02 10.0 1:500   99 83 0.02 2.0 1:100   86 76 0.02 0.4 1:20    74 76 0.02 0.08 1:4     80 76 0.1 10.0 1:100   100 100 0.1 2.0 1:20    100 100 0.1 0.4 1:4     100 100 0.02 10.0 1:500   100 77 0.02 2.0 1:100   100 77 0.02 0.4 1:20    87 77 0.0008 10.0 1:12500 29 0 0.0008 2.0 1:2500  0 0 0.0008 0.4 1:500   0 0 0.1 4.0 1:40    100 100 0.1 0.16  1:1.6    99 100 0.02 4.0 1:200   100 77 0.02 0.16 1:8     85 80 0.004 4.0 1:1000  62 17 0.004 0.16 1:40    45 30 0.0008 4.0 1:5000  0 0 0.0008 0.16 1:200   0 15 0.004 100.0 1:25000 100 100 0.004 20.0 1:5000  84 50 0.004 4.0 1:1000  14 22 0.004 0.8 1:200   40 13 0.02 200.0 1:10000 100 100 0.02 40.0 1:2000  84 82 0.02 8.0 1:400   84 83 0.02 1.6 1:80    90 76

TABLE E3 in vitro-Test with Cordana musae (7.005) (2.005) (2.028) (2.038) (3.025) pyrime- (2.002) fluo- inpyr- isoflu- fenpi- Effi- Colby (I-300) thanil bixafen pyram fluxam cypram coxamid cacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 100 0.02 29 0.004 0 0.0008 0 20.0 24 4.0 0 0.8 0 0.16 0 1.0 0 0.2 0 0.04 2 0.008 0 20.0 8 4.0 1 0.8 0 0.16 6 1.0 0 0.2 0 0.04 0 0.008 0 1.0 22 0.2 0 5.0 80 1.0 40 0.02 20.0 1:1000 35 34 0.02 4.0 1:200  21 13 0.02 0.8 1:40   38 13 0.02 0.16 1:8    17 13 0.004 20.0 1:5000 31 24 0.004 4.0 1:1000 35 0 0.004 0.8 1:200  0 0 0.004 0.16 1:40   0 0 0.1 1.0 1:10   100 100 0.1 0.2 1:2    98 100 0.1 0.04  1:0.4   100 100 0.1 0.008  1:0.08  100 100 0.004 1.0 1:250  45 0 0.004 0.2 1:50   0 0 0.004 0.04 1:10   0 2 0.004 0.008 1:2    15 0 0.02 20.0 1:1000 41 20 0.02 4.0 1:200  26 14 0.02 0.8 1:40   67 13 0.02 0.16 1:8    11 19 0.004 20.0 1:5000 3 8 0.004 4.0 1:1000 24 1 0.004 0.8 1:200  0 0 0.004 0.16 1:40   26 6 0.1 1.0 1:10   100 100 0.1 0.2 1:2    98 100 0.1 0.04  1:0.4   98 100 0.1 0.008  1:0.08  98 100 0.004 1.0 1:250  23 0 0.004 0.2 1:50   18 0 0.004 0.04 1:10   0 0 0.004 0.008 1:2    0 0 0.1 0.2 1:2    100 100 0.02 0.2 1:10   72 28 0.004 0.2 1:50   40 29 0.0008 0.2 1:250  0 0 0.1 1.0 1:10   100 100 0.02 1.0 1:50   58 57 0.004 1.0 1:250  70 57 0.0008 1.0 1:1250 57 40

TABLE E4 in vitro-Test with Cordana musae (1.055) (3.020) (1.002) mefen- (13.001) trifloxy- difeno- triflu- fludio- (5.003) Effi- Colby (I-300) strobin conazole conazole (15.064) xonil captan cacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 100 0.02 29 0.004 0 0.0008 0 1.0 77 0.2 48 0.04 67 1.0 14 0.2 0 1.0 100 0.2 100 0.04 29 0.008 4 10.0 6 2.0 0 5.0 20 1.0 30 0.2 4 20.0 100 4.0 100 0.8 21 0.16 0 0.02 1.0 1:50    83 83 0.02 0.2 1:10    79 62 0.02 0.04 1:2     75 76 0.0008 1.0 1:1250  78 77 0.0008 0.2 1:250   66 48 0.0008 0.04 1:50    79 67 0.1 1.0 1:10    100 100 0.02 1.0 1:50    49 38 0.004 1.0 1:250   46 39 0.0008 1.0 1:1250  30 14 0.02 1.0 1:50    100 100 0.02 0.2 1:10    100 100 0.02 0.04 1:2     43 39 0.02 0.008  1:0.4    25 18 0.0008 1.0 1:1250  100 100 0.0008 0.2 1:250   100 100 0.0008 0.04 1:50    35 29 0.0008 0.008 1:10    14 4 0.1 10.0 1:100   100 100 0.02 10.0 1:500   65 47 0.004 10.0 1:2500  21 16 0.0008 10.0 1:12500 37 30 0.1 5.0 1:50    100 100 0.1 1.0 1:10    99 100 0.1 0.2 1:2     98 100 0.02 5.0 1:250   95 55 0.02 1.0 1:50    81 60 0.02 0.2 1:10    75 46 0.004 5.0 1:1250  23 28 0.004 1.0 1:250   65 37 0.004 0.2 1:50    14 14 0.1 20.0 1:200   100 100 0.1 4.0 1:40    100 100 0.1 0.8 1:8     100 100 0.1 0.16  1:1.6    99 100 0.02 20.0 1:1000  100 100 0.02 4.0 1:200   100 100 0.02 0.8 1:40    53 45 0.02 0.16 1:8     43 30 0.0008 20.0 1:25000 100 100 0.0008 4.0 1:5000  100 100 0.0008 0.8 1:1000  24 24 0.0008 0.16 1:200   18 4

TABLE E5 in vitro-Test with Cordana musae (5.013) (5.018) (17.001) (17.012) man- pro- Bacillus Paeni- (18.001) Effi- Colby (I-300) cozeb pineb subtilis bacillus FLiPPER cacy expected (ppm) (ppm) (ppm) (ppm) terrae (ppm) (ppm) Ratio % value % 0.1 100 0.02 29 0.004 0 0.0008 0 10.0 100 2.0 31 0.4 0 0.08 0 100.0 99 20.0 100 4.0 31 0.8 0 200.0 12 40.0 0 8.0 0 1.6 1 200.0 100 1.6 0 200.0 0 40.0 7 8.0 4 0.02 10.0 1:500    100 100 0.02 2.0 1:100    71 31 0.02 0.4 1:20     12 0 0.02 0.08 1:4      33 0 0.0008 10.0 1:12500  100 100 0.0008 2.0 1:2500   52 31 0.0008 0.4 1:500    19 0 0.0008 0.08 1:100    0 0 0.02 100.0 1:5000   94 99 0.02 20.0 1:1000   100 100 0.02 4.0 1:200    44 31 0.02 0.8 1:40     43 0 0.0008 100.0 1:125000 100 99 0.0008 20.0 1:25000  100 100 0.0008 4.0 1:5000   65 31 0.0008 0.8 1:1000   0 0 0.02 200.0 1:10000  67 37 0.02 40.0 1:2000   30 29 0.02 8.0 1:400    33 29 0.02 1.6 1:80     40 29 0.1 200.0 1:2000   100 100 0.1 1.6 1:16     99 100 0.02 200.0 1:10000  100 100 0.02 1.6 1:80     77 29 0.004 200.0 1:50000  100 100 0.004 1.6 1:400    5 0 0.0008 200.0 1:250000 100 100 0.0008 1.6 1:2000   2 0 0.1 200.0 1:2000   99 100 0.1 40.0 1:400    100 100 0.1 8.0 1:80     98 100 0.02 200.0 1:10000  36 29 0.02 40.0 1:2000   73 33 0.02 8.0 1:400    71 31 0.0008 200.0 1:250000 0 0 0.0008 40.0 1:50000  0 7 0.0008 8.0 1:10000  16 4

TABLE E6 in vitro -Test with Cordana musae (7.005) (2.005) (2.038) (3.020) (1.018) Colby pyrime- (2.002) fluo- isoflu- trifloxy- prothio- Effi- expected (I-302) thanil bixafen pyram cypram strobin conazole cacy value (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % % 0.1 100 0.02 37 0.004 0 0.0008 0 20.0 33 0.8 12 0.16 0 0.2 0 0.04 0 0.008 8 20.0 28 4.0 2 0.16 13 1.0 27 0.2 1 0.04 0 0.008 0 1.0 68 0.2 61 0.008 13 1.0 100 0.2 100 0.04 6 0.02 20.0 1:1000 74 58 0.02 0.8 1:40 57 44 0.02 0.16 1:8 64 37 0.1 0.2 1:2 100 100 0.1 0.04 1:0.4 100 100 0.1 0.008 1:0.08 100 100 0.02 0.2 1:10 61 37 0.02 0.04 1:2 46 37 0.02 0.008 1:0.4 47 40 0.004 0.2 1:50 32 0 0.004 0.04 1:10 2 0 0.004 0.008 1:2 16 6 0.1 20.0 1:200 100 100 0.1 4.0 1:40 99 100 0.1 0.16 1:1.6 100 100 0.02 20.0 1:1000 71 55 0.02 4.0 1:200 57 38 0.02 0.16 1:8 51 45 0.004 20.0 1:5000 42 28 0.004 4.0 1:1000 21 2 0.004 0.16 1:40 3 13 0.02 1.0 27 76 54 0.02 0.2 1 68 38 0.02 0.04 0 67 37 0.02 0.008 0 41 37 0.004 1.0 27 48 27 0.004 0.2 1 0 1 0.004 0.04 0 0 0 0.004 0.008 0 0 0 0.02 1.0 1:50 84 80 0.02 0.2 1:10 80 75 0.02 0.008 1:0.4 56 45 0.004 1.0 1:250 72 68 0.004 0.2 1:50 77 61 0.004 0.008 1:2 0 13 0.0008 1.0 1:1250 72 68 0.0008 0.2 1:250 69 61 0.0008 0.008 1:10 41 13 0.004 1.0 1:250 100 100 0.004 0.2 1:50 100 100 0.004 0.04 1:10 49 10 0.0008 1.0 1:1250 100 100 0.0008 0.2 1:250 100 100 0.0008 0.04 1:50 3 6

TABLE E7 in vitro -Test with Cordana musae (13.001) (13.005) (5.010) Colby fludio- quino- (5.003) dithia- (5.012) Effi- expected (I-302) (15.064) xonil xyfen captan non folpet cacy value (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % % 0.1 100 0.02 37 0.004 0 0.0008 0 10.0 27 2.0 7 5.0 2 1.0 0 0.2 0 0.04 0 10.0 34 2.0 0 0.4 0 0.08 0 4.0 100 0.8 0 0.16 0 4.0 100 0.8 0 0.16 0 2.0 100 0.4 10 0.08 5 0.1 10.0 1:100 100 100 0.1 2.0 1:20 100 100 0.02 10.0 1:500 79 68 0.02 2.0 1:100 67 60 0.004 10.0 1:2500 54 38 0.004 2.0 1:500 37 22 0.0008 10.0 1:12500 28 29 0.0008 2.0 1:2500 22 10 0.02 5.0 1:250 86 57 0.02 1.0 1:50 87 57 0.02 0.2 1:10 74 57 0.02 0.04 1:2 82 57 0.02 10.0 1:500 100 43 0.02 2.0 1:100 75 15 0.02 0.4 1:20 48 15 0.02 0.08 1:4 58 15 0.02 4.0 1:200 100 100 0.02 0.8 1:40 62 15 0.02 0.16 1:8 87 15 0.004 4.0 1:1000 100 100 0.004 0.8 1:200 16 0 0.004 0.16 1:40 0 0 0.02 4.0 1:200 99 100 0.02 0.8 1:40 55 15 0.02 0.16 1:8 26 15 0.004 4.0 1:1000 100 100 0.004 0.8 1:200 7 0 0.004 0.16 1:40 0 0 0.02 2.0 1:100 100 100 0.02 0.4 1:20 80 24 0.02 0.08 1:4 34 19 0.004 2.0 1:500 100 100 0.004 0.4 1:100 28 10 0.004 0.08 1:20 0 5

TABLE E8 in vitro -Test with Cordana musae (5.013) (5.018) (6.002) (17.012) Colby (I-302) mancozeb propineb isotianil Paenibacillus Efficacy expected (ppm) (ppm) (ppm) (ppm) terrae (ppm) Ratio % value % 0.1 100 0.02 37 0.004 0 0.0008 0 10.0 100 2.0 32 0.4 3 0.08 0 20.0 100 4.0 30 0.8 3 20.0 0 4.0 6 0.8 9 40.0 27 8.0 9 1.6 7 0.004 10.0 1:2500 100 100 0.004 2.0 1:500 58 32 0.004 0.4 1:100 0 3 0.004 0.08 1:20 0 0 0.02 20.0 1:1000 100 100 0.02 4.0 1:200 85 71 0.02 0.8 1:40 58 60 0.004 20.0 1:5000 100 100 0.004 4.0 1:1000 69 30 0.004 0.8 1:200 10 3 0.0008 20.0 1:25000 100 100 0.0008 4.0 1:5000 58 30 0.0008 0.8 1:1000 0 3 0.1 20.0 1:200 100 100 0.1 4.0 1:40 100 100 0.1 0.8 1:8 100 100 0.02 20.0 1:5000 53 46 0.02 4.0 1:1000 45 50 0.02 0.8 1:200 57 51 0.004 20.0 1:40 20 0 0.004 4.0 1:25000 8 6 0.004 0.8 1:5000 4 9 0.02 40.0 1:10000 100 100 0.02 8.0 1:2000 74 61 0.02 1.6 1:400 78 51 0.004 40.0 1:50000 100 100 0.004 8.0 1:10000 28 27 0.004 1.6 1:2000 22 9

TABLE E9 in vitro -Test with Cordana musae (3.025) (1.002) fen- (13.001) (2.002) difeno- (5.010) picox- flu- (3.012) Colby (I-339) bixafen conazole dithianon amid dioxonil fluoxa¬strobin Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 100 0.2 100 0.04 100 0.008 63 0.2 0 0.04 0 0.008 0 0.04 0 10 100 0.08 0 0.2 52 0.008 0 5 11 1 0 0.2 0 0.016 0 0.008 0.2 1:25 84 63 0.008 0.04 1:5 62 63 0.008 0.008 1:1 99 63 0.2 0.04 1:0.2 100 100 0.04 0.04 1:1 100 100 0.008 0.04 1:5 85 56 0.04 10 1:250 100 100 0.04 0.08 1:2 100 100 0.008 10 1:1250 100 100 0.008 0.08 1:10 86 56 0.04 0.2 1:5 100 100 0.04 0.008 1:0.2 100 100 0.008 0.2 1:25 82 79 0.008 0.008 1:1 67 56 0.008 5 1:625 93 61 0.008 1 1:125 100 56 0.008 0.2 1:25 99 56 0.2 0.016 1:0.08 100 100 0.04 0.016 1:0.4 100 100 0.008 0.016 1:2 86 82

TABLE E10 in vitro -Test with Cordana musae (17.012) (1.062) (6.002) (5.013) (12.004) (15.016) Paeni- fluoxytio- iso- manco- meta- metra- bacillus Colby (I-339) conazole tianil zeb laxyl-m fenone terrae Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 100 0.2 100 0.04 100 0.008 63 0.2 10 100 7 20 10 4 15 20 100 4 14 0.8 0 0.16 0 100 33 20 0 4 0 0.8 0 5 11 1 0 0.2 0 0.04 0 200 100 40 0 8 0 1.6 0 1 0.2 1:0.2 100 100 0.2 0.2 1:1 100 100 0.008 0.2 1:25 94 84 0.008 100 1:12500 65 58 0.008 20 1:2500 61 59 0.008 4 1:500 69 61 0.008 20 1:2500 100 100 0.008 4 1:500 76 61 0.008 0.8 1:100 79 55 0.008 0.16 1:20 73 55 0.008 100 1:12500 79 70 0.008 20 1:2500 82 55 0.008 4 1:500 71 55 0.008 0.8 1:100 81 55 0.008 5 1:625 97 90 0.008 1 1:125 100 88 0.008 0.2 1:25 96 88 0.008 0.04 1:5 100 88 0.008 200 1:25000 100 100 0.008 40 1:5000 96 88 0.008 8 1:1000 94 88 0.008 1.6 1:200 91 88

TABLE E11 in vitro -Test with Cordana musae (13.004) (1.018) (7.005) (2.017) (5.018) pro- prothio- pyri- Colby (I-339) penflufen propineb quinazid conazole methanil Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 100 0.2 100 0.04 100 0.008 63 5 14 1 0 0.2 0 0.04 0 20 21 4 0 0.8 0 10 15 2 0 0.4 0 0.08 0 0.5 100 0.1 81 0.004 0 20 7 4 7 0.8 40 0.16 0 0.008 5 1:625 93 90 0.008 1 1:125 92 88 0.008 0.2 1:25 92 88 0.008 0.04 1:5 92 88 0.008 20 1:2500 74 33 0.008 4 1:500 85 16 0.008 0.8 1:100 83 16 0.008 10 1:1250 82 29 0.008 2 1:250 83 16 0.008 0.4 1:50 86 16 0.008 0.08 1:10 86 16 0.008 0.5 1:62.5 100 100 0.008 0.1 1:12.5 90 84 0.008 0.004 1:0.5 100 16 0.008 20 1:2500 83 22 0.008 4 1:500 38 22 0.008 0.8 1:100 79 50 0.008 0.16 1:20 81 16

TABLE E12 in vitro -Test with Cordana musae (1.002) (2.002) (5.003) difeno- (5.010) Colby (I-338) (17.001) (1.067) bixafen captan conazole dithianon Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 57 0.2 0 0.04 4 0.008 5 200 0 40 0 2 100 0.4 14 0.08 0 0.016 4 1 2 0.2 0 0.04 0 0.008 17 5 100 1 0 0.04 0 1 20 0.2 16 0.04 0 2 95 1 200 1:200 87 57 1 40 1:40 87 57 0.2 200 1:1000 0 0 0.2 40 1:200 0 0 0.2 2 1:10 100 100 0.2 0.4 1:2 85 14 0.2 0.08 1:0.4 19 0 0.2 0.016 1:0.08 12 4 0.04 2 1:50 100 100 0.04 0.4 1:10 74 18 0.04 0.08 1:2 17 4 0.04 0.016 1:0.4 5 7 0.008 2 1:250 100 100 0.008 0.4 1:50 60 19 0.008 0.08 1:10 8 5 0.008 0.016 1:2 28 8 1 1 1:1 93 58 1 0.2 1:0.2 79 57 1 0.04 1:0.04 86 57 1 0.008 1:0.008 89 64 0.2 1 1:5 46 2 0.2 0.2 1:1 15 0 0.2 0.04 1:0.2 29 0 0.2 0.008 1:0.04 19 17 1 5 1:5 100 100 1 1 1:1 89 57 1 0.04 1:0.04 89 57 0.2 5 1:25 100 100 0.2 1 1:5 36 0 0.2 0.04 1:0.2 31 0 0.04 1 1:25 50 20 0.04 0.2 1:5 16 16 0.04 0.04 1:1 12 0 0.008 1 1:125 32 20 0.008 0.2 1:25 46 16 0.008 0.04 1:5 36 0 1 2 1:2 100 100 0.2 2 1:10 100 96 0.04 2 1:50 100 95 0.008 2 1:250 100 95

TABLE E13 in vitro -Test with Cordana musae (1.062) (3.025) (13.001) (2.005) (15.043) (3.012) fluoxy- fenpicox- fludi- fluo- fluoxa- fluoxa- tiocona- Colby (I-338) amid oxonil pyram piprolin strobin zole Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 100 0.2 6 0.04 0 0.008 0 0.2 44 0.20 0 0.04 6 4 0 0.8 0 20 0 0.16 28 0.08 3 0.016 0 0.008 4 0.2 0.2 1:1 59 47 0.04 0.2 1:5 55 44 0.008 0.2 1:25 50 44 0.2 0.20 1:1 86 6 0.2 0.04 1:0.2 28 12 0.008 0.20 1:25 27 0 0.008 0.04 1:5 26 6 0.04 4 1:100 7 3 0.04 0.8 1:20 20 3 0.008 4 1:500 45 0 0.008 0.8 1:100 19 0 1 20 1:20 84 75 0.2 20 1:100 20 12 0.2 0.16 1:0.8 52 36 0.008 20 1:2500 20 0 1 0.08 1:0.08 99 76 1 0.016 1:0.016 96 75 0.2 0.08 1:0.4 52 15 0.2 0.016 1:0.08 11 12 0.04 0.08 1:2 30 6 0.008 0.08 1:10 9 3 1 0.008 1:0.008 94 76 0.2 0.008 1:0.04 20 16 0.04 0.008 1:0.2 13 7

TABLE E14 in vitro -Test with Cordana musae (15.012) (2.028) (2.038) (5.012) fosetyl- inpyr- isoflucy- (6.002) (5.013) Colby (I-338) folpet al fluxam pram isotianil mancozeb Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 85 0.2 22 0.04 8 0.008 4 1 62 0.2 17 0.04 0 0.008 0 0.8 0 0.2 4 0.04 0 0.008 0 1 20 0.2 9 20 18 4 18 0.8 9 4 19 0.16 18 1 1 1:1 100 94 0.2 1 1:5 87 70 0.2 0.2 1:1 37 36 0.2 0.04 1:0.2 22 22 0.04 0.2 1:5 40 24 0.04 0.04 1:1 34 8 0.008 0.04 1:5 14 4 0.008 0.008 1:1 12 4 1 0.8 1:0.8 97 85 0.2 0.8 1:4 22 22 0.04 0.8 1:20 28 8 0.04 0.2 1:5 15 12 0.04 0.04 1:1 6 8 0.04 0.008 1:0.2 38 8 0.008 0.2 1:25 12 8 0.008 0.04 1:5 35 4 0.008 0.008 1:1 10 4 0.2 1 1:5 52 38 0.2 0.2 1:1 40 29 0.04 1 1:25 30 26 0.04 0.2 1:5 17 16 1 20 1:20 82 82 1 4 1:4 90 82 1 0.8 1:0.8 90 80 1 0.16 1:0.16 93 82 0.2 4 1:20 47 20 0.04 0.16 1:4 24 18

TABLE E15 in vitro -Test with Cordana musae (3.030) (17.012) (12.004) metyl- Paeni- (2.017) (5.018) (13.004) meta- tetra- bacillus pen- pro- pro- Colby (I-338) laxyl-m prole terrae flufen pineb quinazid Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 78 0.2 2 0.04 0 0.008 1 100 16 20 8 4 9 0.8 0 1 70 0.2 19 0.04 0 0.008 0 200 92 5 0 1 0 0.2 0 0.04 0 20 37 0.8 0 10 20 2 16 0.4 3 0.08 5 0.2 100 1:500 40 18 0.2 20 1:100 24 10 0.2 4 1:20 11 11 0.2 0.8 1:4 5 2 0.04 0.2 1:5 32 19 0.04 0.04 1:1 1 0 0.04 0.008 1:0.2 0 0 0.008 1 1:125 73 70 0.008 0.2 1:25 18 19 0.008 0.04 1:5 38 0 0.008 0.008 1:1 0 0 1 200 1:200 100 97 0.2 200 1:1000 100 95 0.04 200 1:5000 100 92 0.008 200 1:25000 99 92 1 5 1:5 81 67 1 1 1:1 74 67 1 0.2 1:0.2 71 67 1 0.04 1:0.04 78 67 1 20 1:20 72 62 1 0.8 1:0.8 87 40 0.2 20 1:100 51 46 0.2 0.8 1:4 20 15 0.04 20 1:500 68 39 0.04 0.8 1:20 2 4 0.008 20 1:2500 67 37 0.008 0.8 1:100 0 0 1 10 1:10 66 51 1 2 1:2 62 49 1 0.4 1:0.4 50 41 1 0.08 1:0.08 74 43

TABLE E16 in vitro -Test with Cordana musae (1.018) (7.005) (13.005) (1.021) prothio- pyri- quinoxy- tebu- Colby (I-338) conazole methanil fen conazole Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 40 0.2 15 0.04 4 0.008 0 0.004 0 20 22 4 30 0.16 17 10 2 0.4 0 0.08 0 1 71 0.2 25 0.04 2 1 0.004 1:0.004 58 40 0.04 0.004 1:0.1 27 4 0.008 0.004 1:0.5 4 0 1 20 1:20 99 53 1 4 1:4 85 58 1 0.16 1:0.16 50 50 0.04 10 1:250 30 13 0.04 0.4 1:10 10 11 0.04 0.08 1:2 18 11 0.2 1 1:5 93 80 0.04 1 1:25 80 74 0.04 0.2 1:5 51 33 0.04 0.04 1:1 21 13

TABLE F2 in vitro -Test with Diaporthe citri (1.055) (7.005) (2.028) (3.020) mefen- (5.013) Colby pyrime- inpyr- trifloxy triflu- (5.003) man- Effi- expected (I-052) thanil fluxam -strobin conazole captan cozeb cacy value (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % % 0.1 100 0.02 100 0.004 0 0.0008 0 20.0 100 4.0 97 0.8 0 0.16 0 1.0 95 0.2 47 0.04 2 0.008 0 1.0 96 0.2 95 0.04 95 0.008 63 1.0 100 0.2 99 0.04 69 0.008 17 4.0 88 0.8 24 0.16 83 10.0 100 2.0 46 0.4 0 0.08 2 0.02 20.0 1:5000 100 100 0.02 4.0 1:1000 97 97 0.02 0.8 1:200 21 0 0.02 0.16 1:40 2 0 0.004 1.0 1:250 94 95 0.004 0.2 1:50 65 47 0.004 0.04 1:10 18 2 0.004 0.008 1:2 10 0 0.004 1.0 1:250 99 96 0.004 0.2 1:50 95 96 0.004 0.04 1:10 94 96 0.004 0.008 1:2 80 67 0.0008 1.0 1:1250 97 96 0.0008 0.2 1:250 94 95 0.0008 0.04 1:50 93 95 0.0008 0.008 1:10 78 63 0.0008 1.0 1:1250 100 100 0.0008 0.2 1:250 100 100 0.0008 0.04 1:50 83 71 0.0008 0.008 1:10 2 23 0.004 4.0 1:1000 100 88 0.004 0.8 1:200 71 24 0.004 0.16 1:40 98 83 0.0008 4.0 1:5000 100 91 0.0008 0.8 1:1000 72 48 0.0008 0.16 1:200 99 88 0.0008 10.0 1:12500 100 100 0.0008 2.0 1:2500 65 47 0.0008 0.4 1:500 0 3 0.0008 0.08 1:100 0 5

TABLE F3 in vitro - Test with Diaporthe citri (5.018) (6.002) (17.001) (17.012) Colby (I-052) propineb isotianil Bacillus Paenibacillus Efficacy expected (ppm) (ppm) (ppm) subtilis (ppm) terrae (ppm) Ratio % value % 0.1 100 0.02 100 0.004 0 0.0008 0 100.0 100 20.0 99 4.0 18 0.8 5 100.0 18 20.0 14 4.0 12 0.8 0 200.0 0 40.0 4 8.0 0 1.6 0 200.0 99 40.0 0 8.0 0 1.6 0 0.0008 100.0 1:125000 100 100 0.0008 20.0 1:25000 100 99 0.0008 4.0 1:5000 41 20 0.0008 0.8 1:1000 5 8 0.004 100.0 1:25000 12 18 0.004 20.0 1:5000 32 14 0.004 4.0 1:1000 20 12 0.004 0.8 1:200 21 0 0.004 200.0 1:50000 17 0 0.004 40.0 1:10000 0 4 0.004 8.0 1:2000 0 0 0.004 1.6 1:400 0 0 0.004 200.0 1:50000 99 99 0.004 40.0 1:10000 18 0 0.004 8.0 1:2000 18 0 0.004 1.6 1:400 0 0

TABLE F4 in vitro - Test with Diaporthe citri Colby (7.005) (2.002) (2.005) (2.028) (2.038) (3.025) expected (I-300) pyrimethanil bixafen fluopyram inpyrfluxam isoflucypram fenpicoxamid Efficacy value (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % % 0.1 44 0.02 22 0.004 10 0.0008 0 4.0 97 0.8 30 0.16 2 1.0 0 0.2 0 0.04 8 0.008 0 20.0 10 4.0 15 0.8 1 0.16 25 1.0 96 0.2 49 0.04 14 0.008 6 1.0 30 0.2 0 0.008 0 5.0 92 1.0 79 0.2 53 0.1 4.0 1:40 100 97 0.1 0.8 1:8 100 30 0.1 0.16 1:1.6 57 2 0.1 1.0 1:10 97 0 0.1 0.2 1:2 100 0 0.1 0.04 1:0.4 100 8 0.1 0.008 1:0.08 99 0 0.1 20.0 1:200 97 10 0.1 4.0 1:40 88 15 0.1 0.8 1:8 76 1 0.1 0.16 1:1.6 81 25 0.1 1.0 1:10 99 96 0.1 0.2 1:2 79 49 0.1 0.04 1:0.4 70 14 0.1 0.008 1:0.08 57 6 0.1 1.0 1:10 82 55 0.1 0.2 1:2 51 35 0.1 0.008 1:0.08 46 35 0.02 1.0 1:50 36 31 0.02 0.2 1:10 5 2 0.02 0.008 1:0.4 12 2 0.1 5.0 1:50 96 95 0.1 1.0 1:10 100 86 0.1 0.2 1:2 87 69 0.02 5.0 1:250 93 92 0.02 1.0 1:50 77 79 0.02 0.2 1:10 65 53 0.0008 5.0 1:6250 92 93 0.0008 1.0 1:1250 83 81 0.0008 0.2 1:250 66 58

TABLE F5 in vitro - Test with Diaporthe citri (1.002) Colby (3.020) difeno- (1.055) (1.018) (1.021) (1.020) expected (I-300) trifloxystrobin conazole mefentrifluconazole prothioconazole tebuconazole spiroxamine Efficacy value (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % % 0.1 44 0.02 22 0.004 10 0.0008 0 0.04 95 0.008 65 1.0 86 0.2 26 0.008 0 1.0 100 0.2 100 0.04 60 0.008 0 1.0 99 0.2 100 0.04 95 0.008 0 1.0 98 0.2 89 0.008 0 4.0 8 0.8 6 0.16 0 0.1 0.04 1:0.4 93 97 0.1 0.008 1:0.08 93 77 0.02 0.04 1:2 96 95 0.02 0.008 1:0.4 93 65 0.004 0.04 1:10 96 97 0.004 0.008 1:2 88 78 0.0008 0.04 1:50 98 95 0.0008 0.008 1:10 85 69 0.1 1.0 1:10 100 91 0.1 0.2 1:2 77 51 0.1 0.008 1:0.08 0 48 0.02 1.0 1:50 98 35 0.02 0.2 1:10 91 87 0.02 0.008 1:0.4 0 2 0.1 1.0 1:10 100 100 0.1 0.2 1:2 99 100 0.1 0.04 1:0.4 83 60 0.1 0.008 1:0.08 67 0 0.02 1.0 1:50 100 100 0.02 0.2 1:10 100 100 0.02 0.04 1:2 66 60 0.02 0.008 1:0.4 0 0 0.0008 1.0 1:1250 99 100 0.0008 0.2 1:250 100 100 0.0008 0.04 1:50 93 63 0.0008 0.008 1:10 0 6 0.0008 1.0 1:1250 100 99 0.0008 0.2 1:250 99 100 0.0008 0.04 1:50 100 96 0.0008 0.008 1:10 0 6 0.1 1.0 1:10 100 98 0.1 0.2 1:2 89 89 0.1 0.008 1:0.08 16 0 0.02 1.0 1:50 98 98 0.02 0.2 1:10 95 89 0.02 0.008 1:0.4 0 0 0.004 1.0 1:250 98 98 0.004 0.2 1:50 89 89 0.004 0.008 1:2 0 0 0.0008 1.0 1:1250 98 98 0.0008 0.2 1:250 94 90 0.0008 0.008 1:10 0 6 0.1 4.0 1:40 94 49 0.1 0.8 1:8 92 47 0.1 0.16 1:1.6 63 44

TABLE F5 in vitro - Test with Diaporthe citri (13.001) (13.004) (13.005) (5.010) Colby fludio- pro- quino- (5.003) dithia- expected (I-300) (15.064) xonil quinazid xyfen captan non Efficacy value (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % % 0.1 44 0.02 22 0.004 10 0.0008 0 2.0 0 0.4 8 0.08 13 5.0 57 1.0 15 0.2 0 10.0 21 0.4 0 0.08 16 10.0 41 2.0 0 0.4 15 4.0 99 0.8 9 0.16 88 20.0 98 4.0 98 0.8 17 0.16 0 0.1 2.0 1:20 100 44 0.1 0.4 1:4 100 49 0.1 0.08 1:0.8 100 51 0.0008 2.0 1:2500 4 0 0.0008 0.4 1:500 34 8 0.0008 0.08 1:100 15 13 0.1 5.0 1:50 96 76 0.1 1.0 1:10 93 53 0.1 0.2 1:2 86 44 0.1 10.0 1:100 100 56 0.1 0.4 1:4 73 44 0.1 0.08 1:0.8 87 53 0.1 10.0 1:100 89 41 0.1 2.0 1:20 49 0 0.1 0.4 1:4 59 15 0.02 10.0 1:500 35 41 0.02 2.0 1:100 33 0 0.02 0.4 1:20 17 15 0.1 4.0 1:40 100 99 0.1 0.8 1:8 99 9 0.1 0.16 1:1.6 97 88 0.02 4.0 1:200 100 99 0.02 0.8 1:40 20 9 0.02 0.16 1:8 100 88 0.004 4.0 1:1000 99 100 0.004 0.8 1:200 27 32 0.004 0.16 1:40 99 91 0.1 20.0 1:200 99 98 0.1 4.0 1:40 98 98 0.1 0.8 1:8 86 17 0.1 0.16 1:1.6 13 0

TABLE F6 in vitro - Test with Diaporthe citri (5.018) (15.016) Colby (5.012) pro- metra- (6.002) (17.001) expected (I-300) folpet pineb fenone isotianil Bacillus Efficacy value (ppm) (ppm) (ppm) (ppm) (ppm) subtilis (ppm) Ratio % % 0.1 44 0.02 22 0.004 10 0.0008 0 10.0 98 2.0 99 0.4 56 0.08 1 100.0 88 20.0 100 4.0 100 0.8 1 20.0 0 4.0 10 0.8 0 0.16 0 100.0 16 20.0 15 4.0 5 0.8 29 200.0 0 40.0 5 8.0 7 1.6 0 0.1 10.0 1:100 100 98 0.1 2.0 1:20 99 99 0.1 0.4 1:4 99 56 0.1 0.08 1:0.8 0 1 0.02 10.0 1:500 97 98 0.02 2.0 1:100 99 99 0.02 0.4 1:20 72 56 0.02 0.08 1:4 14 1 0.1 100.0 1:1000 100 90 0.1 20.0 1:200 96 100 0.1 4.0 1:40 100 100 0.1 0.8 1:8 45 15 0.02 100.0 1:5000 100 88 0.02 20.0 1:1000 100 100 0.02 4.0 1:200 100 100 0.02 0.8 1:40 52 1 0.004 100.0 1:25000 95 88 0.004 20.0 1:5000 100 100 0.004 4.0 1:1000 100 100 0.004 0.8 1:200 6 1 0.0008 100.0 1:125000 100 91 0.0008 20.0 1:25000 100 100 0.0008 4.0 1:5000 100 100 0.0008 0.8 1:1000 35 20 0.1 20.0 1:200 78 14 0.1 4.0 1:40 71 22 0.1 0.8 1:8 80 14 0.1 0.16 1:1.6 56 14 0.02 20.0 1:1000 0 0 0.02 4.0 1:200 20 10 0.02 0.8 1:40 0 0 0.02 0.16 1:8 0 0 0.1 100.0 1:1000 76 16 0.1 20.0 1:200 84 15 0.1 4.0 1:40 77 5 0.1 0.8 1:8 52 29 0.1 200.0 1:2000 96 0 0.1 40.0 1:400 100 5 0.1 8.0 1:80 100 7 0.1 1.6 1:16 99 0

TABLE F7 in vitro - Test with Diaporthe citri (15.012) (17.012) (18.001) (5.013) fosetyl- Colby (I-300) Paenibacillus FLIPPER mancozeb aluminium Efficacy expected (ppm) terrae (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 44 0.02 22 0.004 10 0.0008 0 200.0 99 40.0 0 8.0 0 1.6 18 200.0 0 40.0 6 8.0 1 1.6 1 10.0 100 2.0 100 0.4 21 0.08 6 100.0 30 4.0 23 0.8 0 0.1 200.0 1:2000 99 99 0.1 40.0 1:400 51 0 0.1 8.0 1:80 66 0 0.1 1.6 1:16 29 18 0.1 200.0 1:2000 55 0 0.1 40.0 1:400 96 6 0.1 8.0 1:80 70 1 0.1 1.6 1:16 42 1 0.1 10.0 1:100 100 100 0.1 2.0 1:20 94 100 0.1 0.4 1:4 44 32 0.1 0.08 1:0.8 84 19 0.1 100.0 1:1000 94 39 0.1 4.0 1:200 80 33 0.1 0.8 1:40 33 14

TABLE F8 in vitro - Test with Diaporthe citri (7.005) (2.005) (2.028) (2.038) (3.025) Colby pyrime- (2.002) fluo- inpyr- isoflu- fenpi- expected (I-302) thanil bixafen pyram fluxam cypram coxamid Efficacy value (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % % 0.1 20 0.02 0 0.004 1 0.0008 0 20.0 100 4.0 97 0.8 0 0.16 0 1.0 5 0.2 5 0.04 21 0.008 15 20.0 22 4.0 20 0.8 0 0.16 0 1.0 96 0.2 52 0.04 9 0.008 0 1.0 38 0.2 29 0.04 0 0.008 0 1.0 66 0.2 0 0.04 3 0.1 20.0 1:200 100 100 0.1 4.0 1:40 100 97 0.1 0.8 1:8 100 0 0.1 0.16 1:1.6 99 0 0.1 1.0 1:10 98 5 0.1 0.2 1:2 100 5 0.1 0.04 1:0.4 100 21 0.1 0.008 1:0.08 91 15 0.1 20.0 1:200 100 22 0.1 4.0 1:40 83 20 0.1 0.8 1:8 79 0 0.1 0.16 1:1.6 91 0 0.1 1.0 1:10 96 96 0.1 0.2 1:2 88 52 0.1 0.04 1:0.4 86 9 0.1 0.008 1:0.08 86 0 0.1 1.0 1:10 78 38 0.1 0.2 1:2 84 29 0.1 0.04 1:0.4 52 1 0.1 0.008 1:0.08 80 1 0.1 1.0 1:10 100 66 0.1 0.2 1:2 99 1 0.1 0.04 1:0.4 87 3

TABLE F9 in vitro - Test with Diaporthe citri (1.055) (1.002) mefen- (1.021) difeno- triflu- tebu- (1.020) (13.001) Colby cona- cona- cona- spiro- fludio- expected (I-302) zole zole zole xamine (15.064) xonil Efficacy value (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % % 0.1 20 0.02 0 0.004 1 0.0008 0 1.0 1.0 0.2 0.2 0.04 0.04 0.008 0.008 1.0 100 0.2 100 0.04 38 0.008 0 1.0 99 0.2 96 0.008 28 20.0 0 4.0 0 0.8 0 0.16 0 10.0 0 2.0 0 0.4 0 0.08 3 5.0 0 1.0 0 0.2 0 0.04 0 0.1 1.0 1:10 100 89 0.1 0.2 1:2 74 29 0.1 0.04 1:0.4 14 20 0.1 0.008 1:0.08 61 20 0.1 1.0 1:10 99 100 0.1 0.2 1:2 100 100 0.1 0.04 1:0.4 94 38 0.1 0.008 1:0.08 86 0 0.02 1.0 1:50 100 100 0.02 0.2 1:10 100 100 0.02 0.04 1:2 75 38 0.02 0.008 1:0.4 2 0 0.1 1.0 1:10 100 99 0.1 0.2 1:2 97 96 0.1 0.008 1:0.08 80 28 0.1 20.0 1:200 49 39 0.1 4.0 1:40 100 39 0.1 0.8 1:8 100 39 0.1 0.16 1:1.6 86 39 0.004 20.0 1:5000 14 0 0.004 4.0 1:1000 0 0 0.004 0.8 1:200 12 0 0.004 0.16 1:40 0 0 0.1 10.0 1:100 95 39 0.1 2.0 1:20 99 39 0.1 0.4 1:4 98 39 0.1 0.08 1:0.8 90 41 0.008 10.0 1:12500 12 0 0.008 2.0 1:2500 14 0 0.008 0.4 1:500 9 0 0.008 0.08 1:100 0 3 0.1 5.0 1:50 99 39 0.1 1.0 1:10 98 39 0.1 0.2 1:2 87 39 0.1 0.04 1:0.4 51 39 0.02 5.0 1:250 94 0 0.02 1.0 1:50 0 0 0.02 0.2 1:10 0 0 0.02 0.04 1:2 0 0

TABLE F10 in vitro - Test with Diaporthe citri (13.004) (13.005) (5.010) (5.013) Colby pro- quinoxy- (5.003) dithia- (5.012) man- expected (I-302) quinazid fen captan non folpet cozeb Efficacy value (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % % 0.1 20 0.02 0 0.004 1 0.0008 0 10.0 24 2.0 12 0.4 0 0.08 0 10.0 20 2.0 10 0.4 6 0.08 52 20.0 100 4.0 100 0.8 18 0.16 75 20.0 98 4.0 99 0.8 9 0.16 0 10.0 100 2.0 99 0.4 33 0.08 12 10.0 100 2.0 100 0.4 46 0.08 0 0.1 10.0 1:100 100 54 0.1 2.0 1:20 89 46 0.1 0.4 1:4 86 39 0.1 0.08 1:0.8 88 39 0.02 10.0 1:500 28 24 0.02 2.0 1:100 13 12 0.02 0.4 1:20 13 0 0.02 0.08 1:4 0 0 0.0008 10.0 1:12500 44 24 0.0008 2.0 1:2500 12 12 0.0008 0.4 1:500 9 0 0.0008 0.08 1:100 13 0 0.1 10.0 1:100 85 20 0.1 2.0 1:20 100 10 0.1 0.4 1:4 100 6 0.1 0.08 1:0.8 92 52 0.1 20.0 1:200 100 100 0.1 4.0 1:40 99 100 0.1 0.8 1:8 99 18 0.1 0.16 1:1.6 98 75 0.02 20.0 1:1000 100 100 0.02 4.0 1:200 100 100 0.02 0.8 1:40 45 18 0.02 0.16 1:8 100 75 0.004 20.0 1:5000 100 100 0.004 4.0 1:1000 100 100 0.004 0.8 1:200 36 18 0.004 0.16 1:40 84 75 0.1 20.0 1:200 100 98 0.1 4.0 1:40 99 99 0.1 0.8 1:8 95 9 0.1 0.16 1:1.6 87 0 0.004 20.0 1:5000 97 98 0.004 4.0 1:1000 99 99 0.004 0.8 1:200 23 9 0.004 0.16 1:40 0 0 0.1 10.0 1:100 100 100 0.1 2.0 1:20 100 99 0.1 0.4 1:4 100 33 0.1 0.08 1:0.8 91 12 0.02 10.0 1:500 98 100 0.02 2.0 1:100 99 99 0.02 0.4 1:20 45 33 0.02 0.08 1:4 33 12 0.1 10.0 1:100 99 100 0.1 2.0 1:20 100 100 0.1 0.4 1:4 100 57 0.1 0.08 1:0.8 72 20

TABLE F11 in vitro - Test with Diaporthe citri (15.012) (5.018) fosetyl- (15.016) (6.002) (17.001) (17.012) Colby pro- alumi- metra- iso- Bacillus Paenibacillus expected (I-302) pineb nium fenone tianil subtilis terrae Efficacy value (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % % 0.1 20 0.02 0 0.004 1 0.0008 0 100.0 100 20.0 100 4.0 99 0.8 35 100.0 0 20.0 0 4.0 0 0.8 23 20.0 0 4.0 0 0.8 0 0.16 0 100.0 0 20.0 37 4.0 22 0.8 0 200.0 9 40.0 5 8.0 13 1.6 5 200.0 99 40.0 0 8.0 0 1.6 0 0.1 100.0 1:1000 100 100 0.1 20.0 1:200 100 100 0.1 4.0 1:40 97 100 0.1 0.8 1:8 93 48 0.02 100.0 1:5000 100 100 0.02 20.0 1:1000 100 100 0.02 4.0 1:200 100 99 0.02 0.8 1:40 69 35 0.004 100.0 1:25000 100 100 0.004 20.0 1:5000 100 100 0.004 4.0 1:1000 100 99 0.004 0.8 1:200 51 36 0.0008 100.0 1:125000 100 100 0.0008 20.0 1:25000 100 100 0.0008 4.0 1:5000 99 99 0.0008 0.8 1:1000 36 35 0.1 100.0 1:1000 96 20 0.1 20.0 1:200 44 20 0.1 4.0 1:40 66 20 0.1 0.8 1:8 86 39 0.1 20.0 1:200 88 20 0.1 4.0 1:40 81 20 0.1 0.8 1:8 93 20 0.1 0.16 1:1.6 95 20 0.1 100.0 1:1000 98 60 0.1 20.0 1:200 100 75 0.1 4.0 1:40 100 69 0.1 0.8 1:8 82 60 0.1 200.0 1:2000 92 64 0.1 40.0 1:400 100 62 0.1 8.0 1:80 100 65 0.1 1.6 1:16 100 62 0.1 200.0 1:2000 100 100 0.1 40.0 1:400 85 60 0.1 8.0 1:80 86 60 0.1 1.6 1:16 81 60

TABLE F12 in vitro—Test with Diaporthe citri (17.012) (3.025) (13.001) (15.012) (2.028) (15.016) Paenibacillus Colby (I-339) fenpicoxamid fludioxonil fosetylal inpyrfluxam metrafenone terrae Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 99 0.2 100 0.04 99 0.008 0 1 94 0.2 83 0.008 0 1 9 0.2 0 4 7 0.8 13 1 65 5 0 1 3 200 100 40 0 8 7 1.6 0 0.008 1 1:125 95 94 0.008 0.2 1:25 90 83 0.008 0.008 1:1 29 0 0.2 1 1:5 100 100 0.2 0.2 1:1 100 100 0.008 1 1:125 80 9 0.008 0.2 1:25 0 0 0.2 4 1:20 100 100 0.2 0.8 1:4 100 100 0.008 4 1:500 19 7 0.008 0.8 1:100 20 13 1 1 1:1 100 100 0.2 1 1:5 100 100 0.008 1 1:125 75 65 0.2 5 1:25 100 100 0.2 1 1:5 100 100 0.008 5 1:625 15 6 0.008 1 1:125 18 9 0.008 200 1:25000 100 100 0.008 40 1:5000 32 6 0.008 8 1:1000 19 12 0.008 1.6 1:200 0 6

TABLE F13 in vitro—Test with Diaporthe citri (13.005) (5.010) (3.025) (13.001) (3.012) Colby (I-339) quinoxyfen (I-338) dithianon fenpicoxamid fludioxonil fluoxastrobin Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 99 0.2 100 0.04 99 0.008 0 2 24 0.4 0 0.08 0 1 20 0.2 11 0.04 0 0.008 0 0.4 13 0.2 79 5 0 1 41 2 96 0.4 83 0.04 2 1:50 100 100 0.04 0.4 1:10 100 99 0.04 0.08 1:2 100 99 0.008 2 1:250 48 24 0.008 0.4 1:50 17 0 0.008 0.08 1:10 26 0 1 0.4 1:0.4 33 31 0.2 0.4 1:2 45 23 0.04 0.4 1:10 39 13 0.008 0.4 1:50 14 13 0.2 0.2 1:1 87 82 0.04 0.2 1:5 84 79 0.008 0.2 1:25 87 79 1 5 1:5 71 20 0.2 5 1:25 73 11 0.2 1 1:5 71 47 0.04 5 1:125 69 0 0.008 5 1:625 78 0 0.008 1 1:125 79 41 1 2 1:2 95 96 1 0.4 1:0.4 88 85 0.2 2 1:10 98 97 0.2 0.4 1:2 86 86 0.04 2 1:50 95 96 0.04 0.4 1:10 89 84 0.008 2 1:250 96 96 0.008 0.4 1:50 89 84

TABLE F14 in vitro—Test with Diaporthe citri (6.002) (5.013) (1.055) (12.004) (15.016) (3.030) Colby (I-338) isotianil mancozeb mefentrifluconazole metalaxyl-m metrafenone metyltetraprole Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 2 0.2 0 0.04 0 0.008 0 100 19 20 5 4 9 0.8 10 20 99 4 78 0.8 0 0.16 0 1 99 0.2 94 0.04 21 0.008 8 20 0 4 0 0.8 0 5 0 1 0 0.2 0 0.04 0 0.2 86 1 100 1:100 41 21 1 20 1:20 23 7 1 4 1:4 17 11 1 0.8 1:0.8 36 12 1 20 1:20 99 99 1 4 1:4 81 78 1 0.8 1:0.8 22 2 1 0.16 1:0.16 14 2 0.2 20 1:100 99 99 0.2 4 1:20 79 78 0.2 0.8 1:4 13 0 0.2 0.16 1:0.8 0 0 1 1 1:1 100 99 1 0.2 1:0.2 100 94 0.04 1 1:25 100 99 0.04 0.2 1:5 99 94 0.008 1 1:125 100 99 0.008 0.2 1:25 100 94 0.008 0.04 1:5 35 21 0.008 0.008 1:1 27 8 1 20 1:20 15 2 1 4 1:4 21 2 1 0.8 1:0.8 9 2 1 5 1:5 21 0 1 1 1:1 13 0 1 0.2 1:0.2 10 0 1 0.04 1:0.04 26 0 1 0.2 1:0.2 89 86 0.04 0.2 1:5 90 86 0.008 0.2 1:25 92 86

TABLE F15 in vitro—Test with Diaporthe citri (17.012) Paenibacillus (2.017) (5.018) (13.005) (1.020) (3.020) Colby (I-338) terrae penflufen propineb quinoxyfen spiroxamin trifloxystrobin Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 0 0.2 2 0.04 0 0.008 0 40 0 8 0 1.6 0 5 3 1 0 0.2 2 0.04 0 4 33 10 76 2 13 0.4 0 20 4 4 0 0.008 68 0.2 40 1:200 25 2 0.2 8 1:40 10 2 0.2 1.6 1:8 8 2 0.008 40 1:5000 19 0 0.008 8 1:1000 18 0 0.008 1.6 1:200 0 0 0.2 5 1:25 11 4 0.2 1 1:5 15 2 0.2 0.2 1:1 12 4 0.2 0.04 1:0.2 0 2 0.008 5 1:625 29 3 0.008 1 1:125 7 0 0.008 0.2 1:25 3 2 0.008 0.04 1:5 10 0 1 4 1:4 73 52 0.2 4 1:20 61 48 0.04 4 1:100 83 46 0.008 10 1:1250 84 76 0.008 2 1:250 16 13 0.008 0.4 1:50 31 0 0.04 20 1:500 10 5 0.04 4 1:100 2 2 0.008 20 1:2500 7 4 0.008 4 1:500 15 0 1 0.008 1:0.008 75 73 0.2 0.008 1:0.04 81 68 0.04 0.008 1:0.2 72 68 0.008 0.008 1:1 75 68

TABLE G1 in vitro—Test with Fusarium culmorum Colby (1.055) (5.018) (2.005) (2.028) (3.020) expected (I-052) mefentrifluconazole propineb (I-300) fluopyram inpyrfluxam trifloxystrobin Efficacy value (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % % 0.1 19 0.02 12 0.004 22 0.0008 0 1.0 33 0.2 5 0.04 22 0.008 20 100.0 95 20.0 0 4.0 0 0.8 1 0.0008 1.0 1:1250 100 33 0.0008 0.2 1:250 0 5 0.0008 0.04 1:50 24 22 0.0008 0.008 1:10 28 20 0.1 100.0 1:1000 100 95 0.1 20.0 1:200 2 0 0.1 4.0 1:40 0 0 0.1 0.8 1:8 0 1 0.1 2 0.02 5 0.004 6 0.0008 2 20.0 21 4.0 0 0.8 0 0.16 1 1.0 0 0.2 0 0.04 0 0.008 0 1.0 15 0.2 15 0.04 0 0.1 20.0 1:200 49 21 0.1 4.0 1:40 0 0 0.1 0.8 1:8 0 0 0.1 0.16 1:1.6 0 1 0.0008 20.0 1:25000 53 21 0.0008 4.0 1:5000 0 0 0.0008 0.8 1:1000 7 0 0.0008 0.16 1:200 2 1 0.1 1.0 1:10 41 0 0.1 0.2 1:2 0 0 0.1 0.04 1:0.4 0 0 0.1 0.008 1:0.08 0 0 0.1 1.0 1:10 67 15 0.1 0.2 1:2 43 15 0.1 0.04 1:0.4 0 0 0.02 1.0 1:50 0 28 0.02 0.2 1:10 19 15 0.02 0.04 1:2 35 15 0.004 1.0 1:250 44 0 0.004 0.2 1:50 6 28 0.004 0.04 1:10 17 15

TABLE G2 in vitro—Test with Fusarium culmorum Colby (1.021) (1.020) (13.001) (13.005) (5.010) expected (I-300) tebuconazole spiroxamine (15.064) fludioxonil quinoxyfen dithianon Efficacy value (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % % 0.1 2 0.02 5 0.004 6 0.0008 2 1.0 98 0.2 26 0.04 21 0.008 8 20.0 0 4.0 0 10.0 1 2.0 0 5.0 99 1.0 98 0.2 36 10.0 0 2.0 6 0.4 1 0.08 0 20.0 100 4.0 0 0.1 1.0 1:10 100 98 0.1 0.2 1:2 67 28 0.1 0.04 1:0.4 17 23 0.1 0.008 1:0.08 22 10 0.1 20.0 1:200 44 8 0.1 4.0 1:40 0 8 0.02 20.0 1:1000 13 4 0.02 4.0 1:200 0 4 0.004 20.0 1:5000 24 9 0.004 4.0 1:1000 3 9 0.0008 20.0 1:25000 8 0 0.0008 4.0 1:5000 8 0 0.1 10.0 1:100 45 10 0.1 2.0 1:20 0 8 0.02 10.0 1:500 12 5 0.02 2.0 1:100 0 4 0.0008 10.0 1:12500 24 9 0.0008 2.0 1:2500 13 8 0.1 5.0 1:50 100 99 0.1 1.0 1:10 98 98 0.1 0.2 1:2 48 41 0.1 10.0 1:100 44 0 0.1 2.0 1:20 5 6 0.1 0.4 1:4 0 1 0.1 0.08 1:0.8 0) 0 0.1 20.0 1:200 100 100 0.1 4.0 1:40 100 0 0.02 20.0 1:1000 100 100 0.02 4.0 1:200 97 11 0.004 20.0 1:5000 100 100 0.004 4.0 1:1000 29 12 0.0008 20.0 1:25000 100 100 0.0008 4.0 1:5000 30 0

TABLE G3 in vitro—Test with Fusarium culmorum Colby (5.018) (15.012) (2.005) (3.020) (1.021) expected (I-300) propineb fosetylaluminium (I-302) fluopyram trifloxystrobin tebuconazole Efficacy value (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % % 0.1 2 0.02 5 0.004 6 0.0008 2 100.0 89 20.0 98 4.0 0 0.8 0 100.0 9 20.0 5 4.0 0 0.8 7 0.1 0 0.02 2 0.004 4 0.0008 7 20.0 16 4.0 0 0.8 0 1.0 5 0.2 22 1.0 98 0.2 57 0.04 11 0.1 100.0 1:1000 100 89 0.1 20.0 1:200 93 98 0.1 4.0 1:40 0 0 0.1 0.8 1:8 0 0 0.1 100.0 1:1000 39 9 0.1 20.0 1:200 9 5 0.1 4.0 1:40 0 0 0.1 0.8 1:8 0 7 0.1 20.0 1:200 44 16 0.1 4.0 1:40 0 0 0.1 0.8 1:8 10 0 0.02 20.0 1:1000 25 20 0.02 4.0 1:200 30 5 0.02 0.8 1:40 0 5 0.004 20.0 1:5000 27 26 0.004 4.0 1:1000 9 12 0.004 0.8 1:200 15 12 0.0008 20.0 1:25000 30 19 0.0008 4.0 1:5000 0 3 0.0008 0.8 1:1000 16 3 0.1 1.0 1:10 53 5 0.1 0.2 1:2 26 22 0.02 1.0 1:50 25 7 0.02 0.2 1:10 31 24 0.004 1.0 1:250 10 5 0.004 0.2 1:50 14 22 0.0008 1.0 1:1250 21 6 0.0008 0.2 1:250 26 23 0.02 1.0 1:50 98 98 0.02 0.2 1:10 60 58 0.02 0.04 1:2 44 13 0.004 1.0 1:250 99 98 0.004 0.2 1:50 59 57 0.004 0.04 1:10 24 11

TABLE G4 in vitro—Test with Fusarium culmorum (17.001) Colby (13.001) (13.005) (5.003) (5.012) (5.018) Bacillus expected (I-302) fludioxonil quinoxyfen captan folpet propineb subtilis Efficacy value (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % % 0.1 0 0.02 2 0.004 4 0.0008 7 5.0 99 1.0 83 0.2 0 10.0 0 2.0 0 0.4 0 20.0 100 4.0 100 0.8 0 0.16 0 10.0 100 2.0 100 0.4 0 0.08 0 100.0 82 20.0 98 4.0 0 0.8 0 200.0 0 40.0 2 8.0 7 1.6 6 0.1 5.0 1:50 100 99 0.1 1.0 1:10 92 83 0.1 0.2 1:2 0 0 0.02 5.0 1:250 98 99 0.02 1.0 1:50 92 83 0.02 0.2 1:10 0 0 0.004 5.0 1:1250 99 99 0.004 1.0 1:250 84 82 0.004 0.2 1:50 6 0 0.0008 5.0 1:6250 98 99 0.0008 1.0 1:1250 87 83 0.0008 0.2 1:250 0 0 0.1 10.0 1:100 47 0 0.1 2.0 1:20 0 0 0.1 0.4 1:4 0 0 0.02 10.0 1:500 18 0 0.02 2.0 1:100 6 0 0.02 0.4 1:20 0 0 0.1 20.0 1:200 100 100 0.1 4.0 1:40 100 100 0.1 0.8 1:8 100 0 0.1 0.16 1:1.6 0 0 0.02 20.0 1:1000 100 100 0.02 4.0 1:200 100 100 0.02 0.8 1:40 11 0 0.02 0.16 1:8 0 0 0.004 20.0 1:5000 100 100 0.004 4.0 1:1000 100 100 0.004 0.8 1:200 5 4 0.004 0.16 1:40 2 4 0.1 10.0 1:100 100 100 0.1 2.0 1:20 100 100 0.1 0.4 1:4 16 0 0.1 0.08 1:0.8 0 0 0.02 10.0 1:500 100 100 0.02 2.0 1:100 99 100 0.02 0.4 1:20 4 0 0.02 0.08 1:4 0 0 0.004 10.0 1:2500 100 100 0.004 2.0 1:500 100 100 0.004 0.4 1:100 0 4 0.004 0.08 1:20 0 4 0.1 100.0 1:1000 100 82 0.1 20.0 1:200 95 98 0.1 4.0 1:40 0 0 0.1 0.8 1:8 0 0 0.1 200.0 1:2000 44 0 0.1 40.0 1:400 0 2 0.1 8.0 1:80 1 7 0.1 1.6 1:16 0 6 0.02 200.0 1:10000 5 3 0.02 40.0 1:2000 18 5 0.02 8.0 1:400 2 10 0.02 1.6 1:80 9 9 0.004 200.0 1:50000 12 0 0.004 40.0 1:10000 0 2 0.004 8.0 1:2000 23 7 0.004 1.6 1:400 22 6 0.0008 200.0 1:250000 2 3 0.0008 40.0 1:50000 3 5 0.0008 8.0 1:10000 12 10 0.0008 1.6 1:2000 19 9

TABLE G5 in vitro—Test with Fusarium culmorum (3.025) (13.001) (2.005) (3.012) (1.062) Colby (I-339) (17.001) fenpicoxamid fludioxonil fluopyram fluoxastrobin fluoxytioconazole Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 99 0.2 14 0.04 0 0.008 0 200 0 40 0 8 0 0.008 10 5 98 1 68 0.2 22 0.04 0 4 21 0.16 31 0.08 19 0.016 12 1 27 0.008 12 0.2 200 1:1000 33 14 0.2 40 1:200 32 14 0.2 8 1:40 13 14 0.008 200 1:25000 21 0 0.008 40 1:5000 0 0 0.008 8 1:1000 0 0 1 0.008 1:0.008 100 99 0.2 0.008 1:0.04 66 21 0.008 0.008 1:1 15 17 0.2 5 1:25 97 98 0.2 1 1:5 93 72 0.2 0.2 1:1 89 31 0.2 0.04 1:0.2 60 11 0.04 5 1:125 98 98 0.04 1 1:25 86 68 0.04 0.2 1:5 29 22 0.04 0.04 1:1 0 0 0.008 5 1:625 98 98 0.008 1 1:125 86 71 0.008 0.2 1:25 29 28 0.2 4 1:20 45 33 0.2 0.16 1:0.8 50 42 0.008 4 1:500 29 27 0.008 0.16 1:20 48 37 1 0.08 1:0.08 100 99 1 0.016 1:0.016 100 99 0.2 0.08 1:0.4 33 32 0.2 0.016 1:0.08 88 26 0.008 0.08 1:10 43 26 0.008 0.016 1:2 23 20 1 1 1:1 97 99 1 0.008 1:0.008 100 99 0.2 1 1:5 43 39 0.2 0.008 1:0.04 49 26 0.04 1 1:25 46 29 0.04 0.008 1:0.2 5 14

TABLE G6 in vitro—Test with Fusarium culmorum (15.012) (2.028) (2.038) (12.004) (15.016) (3.030) Colby (I-339) fosetylal inpyrfluxam isoflucypram metalaxyl-m metrafenone metyltetraprole Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 99 0.2 14 0.04 0 0.008 0 0.8 11 1 24 0.04 8 0.008 5 1 24 0.2 10 0.04 0 0.008 0 4 0 0.8 0 1 4 0.2 13 1 0.8 1:0.8 99 99 0.2 0.8 1:4 66 62 0.008 0.8 1:100 11 11 0.2 1 1:5 79 68 0.2 0.04 1:0.2 73 61 0.2 0.008 1:0.04 62 60 0.008 1 1:125 23 24 0.008 0.2 1:25 17 10 0.008 0.04 1:5 13 0 0.008 0.008 1:1 0 0 1 4 1:4 100 99 1 0.8 1:0.8 100 99 0.008 4 1:500 20 10 0.008 0.8 1:100 13 10 1 1 1:1 99 99 0.2 1 1:5 86 53 0.04 1 1:25 1 4 1 0.2 1:0.2 99 99 0.2 0.2 1:1 81 58 0.008 0.2 1:25 24 26

TABLE G7 in vitro—Test with Fusarium culmorum (17.012) Paenibacillus (2.017) (5.018) (13.004) (1.018) (7.005) Colby (I-339) terrae penflufen propineb proquinazid prothioconazole pyrimethanil Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 99 0.2 14 0.04 0 0.008 0 200 99 40 5 8 10 0.04 4 4 12 0.8 2 0.4 0 0.08 18 0.1 98 0.02 52 0.004 6 0.8 5 0.2 200 1:1000 100 100 0.2 40 1:200 55 54 0.2 8 1:40 65 56 1 0.04 1:0.04 100 99 0.2 0.04 1:0.2 73 53 0.2 4 1:20 62 59 0.2 0.8 1:4 72 54 0.008 4 1:500 7 12 0.008 0.8 1:100 15 2 1 0.4 1:0.4 99 99 1 0.08 1:0.08 100 00 0.2 0.4 1:2 55 53 0.2 0.08 1:0.4 66 62 0.008 0.4 1:50 12 0 0.04 0.1 1:2.5 99 98 0.04 0.02 1:0.5 92 54 0.04 0.004 1:0.1 29 10 0.008 0.1 1:12.5 98 98 0.008 0.02 1:2.5 60 52 0.008 0.004 1:0.5 26 6 1 0.8 1:0.8 100 99 0.2 0.8 1:4 67 56 0.008 0.8 1:100 12 5

TABLE G8 in vitro—Test with Fusarium culmorum (1.020) (1.021) (2.002) (1.002) Colby (I-339) spiroxamin tebuconazole (I-338) (1.067) bixafen difenoconazole Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 99 0.2 14 0.04 0 0.008 0 0.8 3 0.16 25 1 79 1 0 0.2 0 0.04 21 0.008 22 2 99 0.4 26 0.08 30 0.016 40 0.04 17 0.008 2 0.04 26 1 0.8 1:0.8 99 99 1 0.16 1:0.16 100 99 0.2 0.8 1:4 54 54 0.2 0.16 1:0.8 66 64 1 1 1:1 98 100 0.2 1 1:5 94 90 0.04 1 1:25 92 79 0.2 2 1:10 99 99 0.2 0.4 1:2 28 26 0.2 0.08 1:0.4 41 30 0.2 0.016 1:0.08 41 40 0.2 0.04 1:0.2 30 17 0.2 0.008 1:0.04 25 2 0.04 0.04 1:1 49 34 0.04 0.008 1:0.2 21 22 1 0.04 1:0.04 27 26 0.2 0.04 1:0.2 50 27 0.04 0.04 1:1 39 29 0.008 0.04 1:5 34 26

TABLE G9 in vitro-Test with Fusarium culmorum (3.025) (13.001) (3.012) (2.028) Colby (5.010) fenpicox- fludioxo- fluoxa- (15.012) inpyr- expected (I-338) dithianon amid nil strobin fosetylal fluxam Efficacy value (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % % 1 0 0.2 1 0.04 4 0.008 0 0.08 4 0.2 18 0.04 1 0.008 7 0.04 0 2 37 100 30 20 11 4 5 0.04 10 1 0.08 1:0.08 20 4 0.2 0.08 1:0.4 24 6 0.04 0.08 1:2 29 8 0.008 0.08 1:10 15 4 0.2 0.2 1:1 24 19 0.2 0.04 1:0.2 23 3 0.2 0.008 1:0.04 18 8 1 0.04 1:0.04 19 0 0.2 0.04 1:0.2 17 1 0.04 0.04 1:1 8 4 0.008 0.04 1:5 0 0 0.2 2 1:10 42 41 0.04 2 1:50 44 43 0.008 2 1:250 43 37 1 100 1:100 33 30 1 20 1:20 22 11 1 4 1:4 18 5 1 0.04 1:0.04 31 10 0.2 0.04 1:0.2 16 15 0.04 0.04 1:1 19 10 0.008 0.04 1:5 31 12

TABLE G10 in vitro-Test with Fusarium culmorum (3.030) (2.038) (5.013) (1.055) (12.004) (15.016) metyl- isoflucy- manco mefentri- meta- metra- tetra- Colby (I-338) pram zeb fluconazole laxyl-m fenone prole Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 0 0.2 6 0.04 0 0.008 1 0.2 19 0.04 10 20 50 0.8 0 1 24 0.04 16 0.008 11 100 22 5 13 1 7 0.2 0 0.04 0 1 8 0.2 6 0.04 8 0.008 7 1 0.2 1:0.2 26 19 1 0.04 1:0.04 16 10 0.2 0.2 1:1 23 23 0.2 0.04 1:0.2 21 15 0.04 0.2 1:5 27 19 0.04 0.04 1:1 9 10 1 20 1:20 86 53 1 0.8 1:0.8 8 5 0.008 20 1:2500 60 54 0.008 0.8 1:100 14 6 0.2 1 1:5 43 24 0.2 0.04 1:0.2 29 16 0.2 0.008 1:0.04 12 11 0.04 0.04 1:1 33 16 0.04 0.008 1:0.2 12 11 1 100 1:100 29 26 0.2 100 1:500 24 22 0.008 100 1:12500 29 27 0.2 5 1:25 22 14 0.2 1 1:5 17 8 0.2 0.2 1:1 7 0 0.2 0.04 1:0.2 17 0 0.04 5 1:125 20 17 0.04 1 1:25 13 11 0.04 0.2 1:5 22 5 0.04 0.04 1:1 16 5 0.04 0.2 1:5 28 11 0.008 1 1:125 20 11 0.008 0.2 1:25 11 10 0.008 0.04 1:5 11 11 0.008 0.008 1:1 16 10

TABLE G11 in vitro-Test with Fusarium culmorum (17.012) Paeni- (2.017) (5.018) (13.004) (1.018) (7.005) bacillus pen- pro- pro- prothio- pyri- Colby (I-338) terrae flufen pineb quinazid conazole methanil Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 11 0.2 0 0.04 5 0.008 3 200 98 5 11 0.2 10 100 49 4 8 10 17 2 8 0.4 11 0.02 22 0.004 22 20 24 0.8 8 0.16 10 1 200 1:200 100 98 0.2 200 1:1000 100 98 0.04 200 1:5000 100 98 1 5 1:5 36 21 1 0.2 1:0.2 21 20 0.2 5 1:25 21 11 0.2 0.2 1:1 28 11 0.04 5 1:125 21 15 0.04 0.2 1:5 35 14 0.008 5 1:625 28 14 0.008 0.2 1:25 16 13 1 100 1:100 63 49 1 4 1:4 11 8 0.04 100 1:2500 54 49 0.04 4 1:100 8 8 1 10 1:10 24 17 1 2 1:2 9 8 1 0.4 1:0.4 16 11 1 0.02 1:0.02 42 22 1 0.004 1:0.004 30 22 0.2 0.02 1:0.1 31 22 0.2 0.004 1:0.02 27 22 0.04 0.02 1:0.5 24 22 0.04 0.004 1:0.1 27 22 0.008 0.02 1:2.5 33 22 0.008 0.004 1:0.5 30 22 1 20 1:20 29 24 1 0.8 1:0.8 25 8 1 0.16 1:0.16 20 10

TABLE G12 in vitro-Test with Fusarium culmorum (13.005) Colby quinoxy- (2.002) (5.003) expected (I-338) fen (I-130) (17.001) (1.067) bixafen captan Efficacy value (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % % 1 13 0.2 21 0.04 13 0.008 4 10 8 0.4 2 0.08 0 1 22 0.2 24 0.04 5 0.008 1 200 18 40 12 1.6 5 2 97 0.08 22 0.016 23 1 18 0.2 11 0.04 7 0.008 2 5 100 1 18 0.2 16 0.04 0 1 10 1:10 25 21 1 0.4 1:0.4 24 15 1 0.08 1:0.08 40 13 1 200 1:200 44 35 1 40 1:40 54 31 1 1.6 1:1.6 24 25 0.008 2 1:250 99 97 0.008 0.08 1:10 29 22 0.008 0.016 1:2 25 23 1 1 1:1 37 36 1 0.04 1:0.04 46 27 0.04 1 1:25 29 22 0.04 0.2 1:5 28 15 0.008 1 1:125 25 18 0.008 0.2 1:25 26 11 0.008 0.04 1:5 24 7 0.008 0.008 1:1 3 2 1 5 1:5 99 100 1 1 1:1 68 36 1 0.04 1:0.04 49 22 0.008 1 1:125 28 19 0.008 0.2 1:25 21 16 0.008 0.04 1:5 0 1

TABLE G13 in vitro-Test with Fusarium culmorum (3.025) (1.062) fen- (13.001) (2.005) (15.043) (3.012) fluoxy- picox- flu- fluo- fluoxa- fluoxa- tiocona- Colby (I-130) amid dioxonil pyram piprolin strobin zole Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 31 0.2 16 0.04 11 0.008 3 1 17 0.2 25 0.04 9 0.008 5 1 88 0.2 26 0.04 0 20 37 0.8 20 0.16 19 4 14 0.8 13 0.4 47 0.08 27 0.016 9 1 30 1 1 1:1 72 50 1 0.2 1:0.2 77 55 1 0.04 1:0.04 78 45 1 0.008 1:0.008 77 43 1 1 1:1 94 93 1 0.2 1:0.2 94 55 1 0.04 1:0.04 67 40 0.04 1 1:25 91 89 0.04 0.2 1:5 69 36 0.008 20 1:2500 42 37 0.008 0.8 1:100 25 20 0.008 0.16 1:20 27 19 0.04 4 1:100 23 21 0.04 0.8 1:20 18 20 0.008 4 1:500 20 14 0.008 0.8 1:100 23 13 1 0.4 1:2 72 66 1 0.08 1:0.4 56 54 1 0.016 1:0.08 58 43 1 1 1:1 60 56 0.2 1 1:5 57 48 0.04 1 1:25 51 35 0.008 1 1:125 33 30

TABLE G14 in vitro-Test with Fusarium culmorum (1.055) (2.038) (5.013) mefen- (12.004) (15.016) isoflucy- (6.002) manco- triflu- meta- metra- Colby (I-130) pram isotianil zeb conazole laxyl-m fenone Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 31 0.2 16 0.04 11 0.008 3 0.2 20 100 20 20 14 4 16 0.8 7 20 31 4 16 0.8 0 0.16 0 1 33 0.04 24 0.008 3 100 23 5 13 1 13 0.2 0 0.04 0 0.04 0.2 1:5 41 30 0.008 0.2 1:25 25 25 1 100 1:100 54 33 1 20 1:20 50 29 1 4 1:4 43 30 1 0.8 1:0.8 31 23 1 20 1:20 86 43 1 4 1:4 49 30 1 0.8 1:0.8 46 17 1 0.16 1:0.16 43 17 0.2 20 1:100 60 40 0.04 20 1:500 47 39 0.008 20 1:2500 52 37 0.04 0.04 1:1 37 33 0.04 0.008 1:0.2 14 15 0.008 1 1:125 43 39 0.008 0.008 1:1 15 11 1 100 1:100 56 37 0.008 100 1:12500 34 30 1 5 1:5 86 29 1 1 1:1 57 29 1 0.2 1:0.2 25 19 1 0.04 1:0.04 21 19

TABLE G15 in vitro-Test with Fusarium culmorum (3.030) (17.012) metyl- Paeni- (2.017) (5.018) (13.004) (1.018) (7.005) tetra- bacillus pen- pro- pro- prothio- pyri- Colby (I-130) prole terrae flufen pineb quinazid conazole methanil Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 19 0.2 0 0.04 0 0.008 0 1 2 0.2 5 0.04 0 0.008 0 200 100 40 38 8 20 1.6 4 5 8 1 11 0.2 2 100 97 4 9 0.8 6 10 1 2 7 0.08 2 0.02 23 20 21 4 16 1 1 1:1 49 20 1 0.2 1:0.2 43 22 1 0.04 1:0.04 48 19 1 0.008 1:0.008 46 19 0.008 1 1:125 11 2 0.008 0.2 1:25 23 5 0.008 0.04 1:5 16 0 0.008 0.008 1:1 18 0 1 200 1:200 100 100 1 40 1:40 56 49 1 8 1:8 46 35 1 1.6 1:1.6 36 22 1 5 1:5 41 25 1 1 1:1 30 28 1 0.2 1:0.2 30 20 0.04 5 1:125 32 8 0.04 1 1:25 23 11 0.04 0.2 1:5 8 2 0.008 5 1:625 21 8 0.008 1 1:125 28 11 0.008 0.2 1:25 20 2 0.008 100 1:12500 97 97 0.008 4 1:500 11 9 0.008 0.8 1:100 11 6 1 10 1:10 60 42 0.2 10 1:50 9 1 0.04 10 1:250 4 1 0.04 0.08 1:2 14 2 0.008 10 1:1250 9 1 0.008 2 1:250 17 7 0.008 0.08 1:10 19 2 1 0.02 1:0.02 76 55 0.2 0.02 1:0.1 27 23 1 20 1:20 54 53 1 4 1:4 55 51 0.008 20 1:2500 22 21 0.008 4 1:500 20 16

TABLE H1 in vitro-Test with Parastagonospora nodorum (1.055) mefen- (17.012) (7.005) triflu- (1.020) (13.001) (5.018) Paeni- Colby pyrime- cona- spiro- fludio- pro- bacillus expected (I-052) thanil zole xamine xonil pineb terrae Efficacy value (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % % 0.1 100 0.02 7 0.004 0 0.0008 0 20.0 100 4.0 100 0.8 100 0.16 17 1.0 100 0.2 100 0.04 97 0.008 90 20.0 7 4.0 4 0.8 2 0.16 3 5.0 64 1.0 38 0.2 0 0.04 0 100.0 100 20.0 60 4.0 25 0.8 13 200.0 86 40.0 6 8.0 4 1.6 1 0.02 20.0 1:1000 100 100 0.02 4.0 1:200 98 100 0.02 0.8 1:40 100 100 0.02 0.16 1:8 98 19 0.004 20.0 1:5000 100 100 0.004 4.0 1:1000 100 100 0.004 0.8 1:200 100 100 0.004 0.16 1:40 100 17 0.0008 20.0 1:25000 100 100 0.0008 4.0 1:5000 100 100 0.0008 0.8 1:1000 100 100 0.0008 0.16 1:200 100 17 0.1 1.0 1:1250 100 100 0.1 0.2 1:250 100 100 0.1 0.04 1:50 97 97 0.1 0.008 1:10 97 90 0.02 20.0 1:1000 46 18 0.02 4.0 1:200 23 15 0.02 0.8 1:40 25 13 0.02 0.16 1:8 22 14 0.02 5.0 1:250 100 68 0.02 1.0 1:50 91 45 0.02 0.2 1:10 65 11 0.02 0.04 1:2 15 11 0.0008 5.0 1:6250 66 64 0.0008 1.0 1:1250 53 38 0.0008 0.2 1:250 0 0 0.0008 0.04 1:50 0 0 0.02 100.0 1:5000 100 100 0.02 20.0 1:1000 69 63 0.02 4.0 1:200 53 31 0.02 0.8 1:40 21 19 0.02 200.0 1:10000 100 88 0.02 40.0 1:2000 29 22 0.02 8.0 1:400 15 21 0.02 1.6 1:80 13 18 0.0008 200.0 1:250000 99 86 0.0008 40.0 1:50000 14 6 0.0008 8.0 1:10000 0 4 0.0008 1.6 1:2000 8 1

TABLE H2 in vitro-Test with Parastagonospora nodorum (3.025) (1.055) (7.005) (2.005) fenpi- (1.002) mefen- Colby pyrime- (2.002) fluo- coxa- difeno- triflu- expected (I-300) thanil bixafen pyram mid conazole conazole Efficacy value (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % % 0.1 100 0.02 7 0.004 0 0.0008 0 20.0 100 4.0 100 0.8 100 0.16 17 1.0 41 0.2 28 0.04 8 0.008 0 20.0 70 4.0 44 0.8 37 0.16 8 5.0 72 1.0 64 0.2 61 0.04 19 1.0 97 0.2 88 0.04 22 0.008 0 1.0 100 0.2 99 0.04 99 0.008 89 0.02 20.0 1:1000 100 100 0.02 4.0 1:200 100 100 0.02 0.8 1:40 100 100 0.02 0.16 1:8 100 23 0.004 20.0 1:5000 100 100 0.004 4.0 1:1000 100 100 0.004 0.8 1:200 100 100 0.004 0.16 1:40 98 17 0.004 1.0 1:250 56 41 0.004 0.2 1:50 32 28 0.004 0.04 1:10 0 8 0.004 0.008 1:2 0 0 0.0008 20.0 1:25000 79 70 0.0008 4.0 1:5000 46 44 0.0008 0.8 1:1000 38 37 0.0008 0.16 1:200 3 8 0.02 5.0 1:250 76 73 0.02 1.0 1:50 69 65 0.02 0.2 1:10 66 62 0.02 0.04 1:2 30 20 0.004 5.0 1:1250 78 72 0.004 1.0 1:250 67 64 0.004 0.2 1:50 59 61 0.004 0.04 1:10 23 19 0.0008 5.0 1:6250 74 72 0.0008 1.0 1:1250 66 64 0.0008 0.2 1:250 64 61 0.0008 0.04 1:50 30 19 0.02 1.0 1:50 97 97 0.02 0.2 1:10 95 88 0.02 0.04 1:2 20 23 0.02 0.008 1:0.4 0 1 0.02 1.0 1:50 100 100 0.02 0.2 1:10 100 99 0.02 0.04 1:2 100 99 0.02 0.008 1:0.4 100 89 0.0008 1.0 1:1250 100 100 0.0008 0.2 1:250 100 99 0.0008 0.04 1:50 100 99 0.0008 0.008 1:10 98 89

TABLE H3 in vitro-Test with Parastagonospora nodorum (13.001) (5.018) (17.001) (7.005) Colby fludio- pro- Bacillus pyrime- (2.002) expected (I-300) xonil pineb subtilis (I-302) thanil bixafen Efficacy value (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % % 0.1 100 0.02 7 0.004 0 0.0008 0 5.0 73 1.0 49 0.2 0 0.04 0 100.0 98 20.0 100 4.0 53 0.8 15 200.0 90 40.0 0 8.0 1 1.6 1 0.1 100 0.02 0 0.004 0 0.0008 0 20.0 100 4.0 100 0.8 100 0.16 71 1.0 44 0.2 34 0.04 4 0.008 1 0.02 5.0 1:250 93 73 0.02 1.0 1:50 66 49 0.02 0.2 1:10 0 0 0.02 0.04 1:2 0 0 0.0008 5.0 1:6250 81 73 0.0008 1.0 1:1250 48 49 0.0008 0.2 1:250 0 0 0.0008 0.04 1:50 0 0 0.02 100.0 1:5000 100 99 0.02 20.0 1:1000 100 100 0.02 4.0 1:200 66 56 0.02 0.8 1:40 24 19 0.004 100.0 1:25000 96 98 0.004 20.0 1:5000 100 100 0.004 4.0 1:1000 65 53 0.004 0.8 1:200 20 15 0.0008 100.0 1:125000 99 98 0.0008 20.0 1:25000 100 100 0.0008 4.0 1:5000 61 54 0.0008 0.8 1:1000 22 16 0.1 200.0 1:2000 100 100 0.1 40.0 1:400 99 100 0.1 8.0 1:80 99 100 0.1 1.6 1:16 98 100 0.02 200.0 1:10000 96 90 0.02 40.0 1:2000 0 0 0.02 8.0 1:400 0 1 0.02 1.6 1:80 0 1 0.004 200.0 1:50000 100 90 0.004 40.0 1:10000 2 0 0.004 8.0 1:2000 0 1 0.004 1.6 1:400 0 1 0.0008 200.0 1:250000 100 90 0.0008 40.0 1:50000 1 0 0.0008 8.0 1:10000 0 1 0.0008 1.6 1:2000 0 1 0.02 20.0 1:1000 100 100 0.02 4.0 1:200 100 100 0.02 0.8 1:40 100 100 0.02 0.16 1:8 100 73 0.0008 1.0 1:1250 56 44 0.0008 0.2 1:250 35 34 0.0008 0.04 1:50 5 4 0.0008 0.008 1:10 2 1

TABLE H4 in vitro-Test with Parastagonospora nodorum (13.001) (5.013) (5.018) (17.012) Colby fludio- man- pro- Paeni- (18.001) expected (I-302) xonil cozeb pineb bacillus FLIPPER Efficacy value (ppm) (ppm) (ppm) (ppm) terrae (ppm) (ppm) Ratio % % 0.1 100 0.02 0 0.004 0 0.0008 0 5.0 76 1.0 51 0.2 0 0.04 0 10.0 100 2.0 37 0.4 5 0.08 0 100.0 100 20.0 100 4.0 62 0.8 22 200.0 93 40.0 0 8.0 1 1.6 0 200.0 17 40.0 9 8.0 2 1.6 0 0.1 5.0 1:50 100 100 0.1 1.0 1:10 99 100 0.1 0.2 1:2 99 100 0.1 0.04 1:0.4 100 100 0.02 5.0 1:250 100 76 0.02 1.0 1:50 93 51 0.02 0.2 1:10 0 0 0.02 0.04 1:2 0 0 0.004 5.0 1:1250 80 76 0.004 1.0 1:250 58 51 0.004 0.2 1:50 0 0 0.004 0.04 1:10 0 0 0.0008 5.0 1:6250 82 76 0.0008 1.0 1:1250 50 51 0.0008 0.2 1:250 0 0 0.0008 0.04 1:50 0 0 0.1 10.0 1:100 100 100 0.1 2.0 1:20 99 100 0.1 0.4 1:4 99 100 0.1 0.08 1:0.8 100 100 0.02 10.0 1:500 100 100 0.02 2.0 1:100 54 37 0.02 0.4 1:20 11 5 0.02 0.08 1:4 5 0 0.004 10.0 1:2500 100 100 0.004 2.0 1:500 47 37 0.004 0.4 1:100 2 5 0.004 0.08 1:20 1 0 0.0008 10.0 1:12500 100 100 0.0008 2.0 1:2500 49 37 0.0008 0.4 1:500 7 5 0.0008 0.08 1:100 4 0 0.02 100.0 1:5000 100 100 0.02 20.0 1:1000 100 100 0.02 4.0 1:200 69 62 0.02 0.8 1:40 42 22 0.004 100.0 1:25000 100 100 0.004 20.0 1:5000 100 100 0.004 4.0 1:1000 72 62 0.004 0.8 1:200 36 22 0.0008 100.0 1:125000 100 100 0.0008 20.0 1:25000 100 100 0.0008 4.0 1:5000 64 62 0.0008 0.8 1:1000 28 22 0.02 200.0 1:10000 100 93 0.02 40.0 1:2000 11 3 0.02 8.0 1:400 0 5 0.02 1.6 1:80 0 3 0.004 200.0 1:50000 96 93 0.004 40.0 1:10000 5 0 0.004 8.0 1:2000 0 1 0.004 1.6 1:400 0 0 0.0008 200.0 1:250000 100 93 0.0008 40.0 1:50000 0 0 0.0008 8.0 1:10000 1 1 0.0008 1.6 1:2000 0 0 0.1 200.0 1:2000 99 100 0.1 40.0 1:400 99 100 0.1 8.0 1:80 99 100 0.1 1.6 1:16 99 100 0.02 200.0 1:10000 24 20 0.02 40.0 1:2000 35 12 0.02 8.0 1:400 15 6 0.02 1.6 1:80 0 3 0.0008 200.0 1:250000 19 17 0.0008 40.0 1:50000 11 9 0.0008 8.0 1:10000 4 2 0.0008 1.6 1:2000 0 0

TABLE H5 in vitro-Test with Parastagonospora nodorum (13.001) (13.005) (1.020) (1.021) Colby (5.003) (5.010) fludioxo- quinoxy- spirox- tebu- expected (I-339) captan dithianon nil fen amin conazole Efficacy value (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % % 1 100 0.2 100 0.04 100 0.008 55 5 75 2 96 0.4 5 0.08 12 5 98 0.2 18 10 33 2 1 0.4 4 0.08 5 20 17 4 5 0.8 5 0.16 9 1 100 0.2 60 0.04 0 0.008 0 0.2 5 1:25 100 100 0.04 5 1:125 100 100 0.008 5 1:625 100 89 0.04 2 1:50 100 100 0.04 0.4 1:10 100 96 0.04 0.08 1:2 100 96 0.04 5 1:125 100 100 0.04 0.2 1:5 100 96 0.008 5 1:625 99 99 0.008 0.2 1:25 95 81 0.2 10 1:50 100 73 0.2 2 1:10 100 61 0.2 0.4 1:2 100 62 0.2 0.08 1:0.4 100 62 0.2 20 1:100 100 67 0.2 4 1:20 100 62 0.2 0.8 1:4 100 62 0.2 0.16 1:0.8 100 64 0.2 1 1:5 100 100 0.2 0.2 1:1 100 84 0.2 0.04 1:0.2 99 60 0.2 0.008 1:0.04 100 60

TABLE H6 in vitro-Test with Parastagonospora nodorum (3.020) (5.003) (1.002) (13.001) Colby (I-339) trifloxystrobin (I-338) (1.067) captan difenoconazole fludioxonil Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 100 0.2 100 0.04 100 0.008 55 1 87 0.2 83 0.04 54 0.008 17 1 100 0.2 12 0.04 10 0.008 8 0.4 100 0.08 94 0.016 0 5 100 0.04 0 0.2 100 0.04 100 0.008 32 0.04 1 0.2 1 1:5 100 95 0.2 0.2 1:1 100 93 0.2 0.04 1:0.2 100 82 0.2 0.008 1:0.04 100 67 0.2 0.4 1:2 100 100 0.2 0.08 1:0.4 100 95 0.2 0.016 1:0.08 15 12 0.04 0.4 1:10 100 100 0.04 0.08 1:2 100 95 0.04 0.016 1:0.4 9 10 0.2 5 1:25 100 100 0.2 0.04 1:0.2 13 12 0.008 5 1:625 100 100 0.008 0.04 1:5 60 8 0.008 0.2 1:25 100 100 0.008 0.04 1:5 100 100 0.008 0.008 1:1 50 42 1 0.04 1:0.04 98 97 0.2 0.04 1:0.2 27 25 0.04 0.04 1:1 6 7 0.008 0.04 1:5 61 16

TABLE H7 in vitro-Test with Parastagonospora nodorum (1.055) (15.016) (3.030) (2.005) mefen- metra- metyl- (5.018) (13.004) Colby (I-338) fluopyram trifluconazole fenone tetraprole propineb proquinazid Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 84 0.2 13 0.04 8 0.008 3 20 59 4 35 0.04 99 0.008 84 5 32 1 0 0.2 0 0.04 0 1 84 0.04 38 4 64 0.8 26 0.08 32 0.2 20 1:100 86 64 0.04 4 1:100 45 40 0.008 20 1:2500 63 60 0.008 4 1:500 37 36 0.04 0.04 1:1 99 99 0.04 0.008 1:0.2 97 86 0.008 0.04 1:5 99 99 0.008 0.008 1:1 90 86 0.04 5 1:125 47 32 0.04 1 1:25 3 0 0.04 0.2 1:5 2 0 0.04 0.04 1:1 12 0 0.04 1 1:25 89 84 0.04 0.04 1:1 43 38 0.008 1 1:125 82 84 0.008 0.04 1:5 44 38 1 4 1:4 87 88 1 0.8 1:0.8 80 75 0.008 4 1:500 60 64 0.008 0.8 1:100 71 26 1 0.08 1:0.08 100 78 0.2 0.08 1:0.4 100 44 0.04 0.08 1:2 100 43 0.008 0.08 1:10 81 32

TABLE H8 in vitro-Test with Parastagonospora nodorum (1.021) (13.001) (2.005) (12.004) (2.017) Colby (I-338) tebuconazole (I-130) fludioxonil fluopyram metalaxyl-m penflufen Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 94 0.2 24 0.04 9 0.008 1 1 99 0.2 63 0.04 0 0.008 0 1 100 0.2 100 0.04 100 0.008 81 1 58 0.2 40 0.04 0 0.16 0 20 3 4 8 0.8 12 0.2 5 0.04 0 0.008 1 1:125 99 99 0.008 0.2 1:25 70 63 0.008 0.04 1:5 0 1 0.008 0.008 1:1 7 1 0.008 1 1:125 93 92 0.008 0.2 1:25 98 89 0.008 0.04 1:5 95 81 0.2 0.16 1:0.8 100 100 0.04 0.16 1:4 100 100 0.008 0.16 1:20 80 78 1 20 1:20 100 99 1 4 1:4 100 99 1 0.8 1:0.8 100 99 0.04 0.2 1:5 100 100 0.04 0.04 1:1 100 100 0.008 0.2 1:25 89 86 0.008 0.04 1:5 92 86

TABLE I1 in vitro-Test with Ustilago segetum var. avenae (2.002) (2.038) (3.020) (1.002) (13.001) (5.012) Colby (I-052) bixafen isoflucypram trifloxystrobin difenoconazole fludioxonil folpet Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 0 0.02 0 0.004 3 0.0008 2 1.0 100 0.2 100 0.04 0 0.008 0 1.0 100 0.2 100 0.04 22 0.008 6 1.0 64 0.2 52 0.008 19 1.0 100 0.2 45 0.04 14 0.008 8 5.0 100 1.0 100 0.2 75 0.04 19 10.0 100 2.0 100 0.4 15 0.08 12 0.1 1.0 1:10 100 100 0.1 0.2 1:2 99 100 0.1 0.04 1:0.4 18 0 0.1 0.008 1:0.08 0 0 0.02 1.0 1:50 100 100 0.02 0.2 1:10 98 100 0.02 0.04 1:2 0 0 0.02 0.008 1:0.4 0 0 0.02 1.0 1:50 100 100 0.02 0.2 1:10 100 100 0.02 0.04 1:2 50 22 0.02 0.008 1:0.4 0 6 0.004 1.0 1:250 100 100 0.004 0.2 1:50 100 100 0.004 0.04 1:10 31 22 0.004 0.008 1:2 0 7 0.004 1.0 1:250 74 64 0.004 0.2 1:50 56 52 0.004 0.008 1:2 18 20 0.0008 1.0 1:1250 74 64 0.0008 0.2 1:250 58 53 0.0008 0.008 1:10 17 21 0.02 1.0 1:50 100 100 0.02 0.2 1:10 87 45 0.02 0.04 1:2 20 14 0.02 0.008 1:0.4 0 8 0.0008 1.0 1:1250 100 100 0.0008 0.2 1:250 51 46 0.0008 0.04 1:50 22 16 0.0008 0.008 1:10 20 10 0.1 5.0 1:50 100 100 0.1 1.0 1:10 100 100 0.1 0.2 1:2 100 75 0.1 0.04 1:0.4 23 19 0.02 5.0 1:250 100 100 0.02 1.0 1:50 100 100 0.02 0.2 1:10 100 75 0.02 0.04 1:2 29 19 0.1 10.0 1:100 100 100 0.1 2.0 1:20 100 100 0.1 0.4 1:4 20 15 0.1 0.08 1:0.8 14 12 0.02 10.0 1:500 100 100 0.02 2.0 1:100 100 100 0.02 0.4 1:20 29 15 0.02 0.08 1:4 7 12

TABLE I2 in vitro-Test with Ustilago segetum var. avenae (5.013) (5.018) (2.005) (2.038) (3.025) Colby (I-052) mancozeb propineb (I-300) fluopyram isoflucypram fenpicoxamid Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 0 0.02 0 0.004 3 0.0008 2 10.0 98 2.0 10 0.4 0 0.08 3 100.0 82 20.0 98 4.0 12 0.8 3 0.1 10.0 1:100 100 98 0.1 2.0 1:20 85 10 0.1 0.4 1:4 0 0 0.1 0.08 1:0.8 0 3 0.02 10.0 1:500 96 98 0.02 2.0 1:100 29 10 0.02 0.4 1:20 0 0 0.02 0.08 1:4 0 3 0.1 100.0 1:1000 100 82 0.1 20.0 1:200 98 98 0.1 4.0 1:40 40 12 0.1 0.8 1:8 1 3 0.1 0 0.02 0 0.004 0 0.0008 0 20.0 10 4.0 10 0.8 9 0.16 15 1.0 100 0.2 100 0.04 85 0.008 0 5.0 0 1.0 0 0.2 0 0.04 0 0.02 20.0 1:1000 11 10 0.02 4.0 1:200 18 10 0.02 0.8 1:40 19 9 0.02 0.16 1:8 26 15 0.004 20.0 1:5000 11 10 0.004 4.0 1:1000 13 10 0.004 0.8 1:200 13 10 0.004 0.16 1:40 22 15 0.1 1.0 1:10 100 100 0.1 0.2 1:2 100 100 0.1 0.04 1:0.4 100 85 0.1 0.008 1:0.08 0 0 0.02 1.0 1:50 100 100 0.02 0.2 1:10 100 100 0.02 0.04 1:2 98 85 0.02 0.008 1:0.4 7 0 0.004 1.0 1:250 100 100 0.004 0.2 1:50 100 100 0.004 0.04 1:10 99 85 0.004 0.008 1:2 2 0 0.1 5.0 1:50 86 0 0.1 1.0 1:10 98 0 0.1 0.2 1:2 0 0 0.1 0.04 1:0.4 0 0

TABLE I3 in vitro-Test with Ustilago segetum var. avenae (1.002) (1.055) difeno- mefen- (13.001) (5.003) (5.010) (5.012) Colby (I-300) conazole trifluconazole fludioxonil captan dithianon folpet Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 0 0.02 0 0.004 0 0.0008 0 1.0 100 0.2 85 0.04 12 0.008 10 1.0 100 0.2 100 0.04 4 0.008 0 5.0 100 1.0 100 0.2 0 20.0 67 4.0 13 0.8 0 0.16 3 20.0 99 4.0 100 0.8 12 0.16 5 10.0 100 2.0 100 0.4 19 0.08 13 0.1 1.0 1:10 100 100 0.1 0.2 1:2 100 85 0.1 0.04 1:0.4 49 12 0.1 0.008 1:0.08 4 10 0.02 1.0 1:50 100 100 0.02 0.2 1:10 90 85 0.02 0.04 1:2 17 12 0.02 0.008 1:0.4 12 10 0.02 1.0 1:50 100 100 0.02 0.2 1:10 100 100 0.02 0.04 1:2 8 4 0.02 0.008 1:0.4 0 0 0.0008 1.0 1:1250 100 100 0.0008 0.2 1:250 100 100 0.0008 0.04 1:50 76 4 0.0008 0.008 1:10 16 0 0.1 5.0 1:50 100 100 0.1 1.0 1:10 100 100 0.1 0.2 1:2 100 0 0.02 5.0 1:250 100 100 0.02 1.0 1:50 100 100 0.02 0.2 1:10 68 0 0.1 20.0 1:200 100 67 0.1 4.0 1:40 10 13 0.1 0.8 1:8 0 0 0.1 0.16 1:1.6 0 3 0.1 20.0 1:200 100 99 0.1 4.0 1:40 100 100 0.1 0.8 1:8 22 12 0.1 0.16 1:1.6 11 5 0.02 20.0 1:1000 100 99 0.02 4.0 1:200 100 100 0.02 0.8 1:40 13 12 0.02 0.16 1:8 15 5 0.004 20.0 1:5000 100 99 0.004 4.0 1:1000 100 100 0.004 0.8 1:200 15 12 0.004 0.16 1:40 10 5 0.1 10.0 1:100 100 100 0.1 2.0 1:20 100 100 0.1 0.4 1:4 55 19 0.1 0.08 1:0.8 22 13 0.02 10.0 1:500 100 100 0.02 2.0 1:100 100 100 0.02 0.4 1:20 42 19 0.02 0.08 1:4 20 13 0.004 10.0 1:2500 100 100 0.004 2.0 1:500 100 100 0.004 0.4 1:100 37 20 0.004 0.08 1:20 14 14 0.0008 10.0 1:12500 100 100 0.0008 2.0 1:2500 100 100 0.0008 0.4 1:500 26 19 0.0008 0.08 1:100 13 13

TABLE I4 in vitro-Test with Ustilago segetum var. avenae (17.001) (3.020) Bacillus (2.038) tri- (1.020) (13.001) Colby (I-300) subtilis (I-302) isoflucypram floxystrobin spiroxamine fludioxonil Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 0 0.02 0 0.004 0 0.0008 0 200.0 0 40.0 0 8.0 0 1.6 0 0.1 200.0 1:2000 28 0 0.1 40.0 1:400 0 0 0.1 8.0 1:80 0 0 0.1 1.6 1:16 0 0 0.1 0 0.02 0 0.004 0 0.0008 0 1.0 100 0.2 100 0.04 24 0.008 0 5.0 100 1.0 54 0.2 0 0.04 0 20.0 100 4.0 71 0.8 3 0.16 7 5.0 100 1.0 100 0.2 12 0.04 16 0.1 1.0 1:10 99 100 0.1 0.2 1:2 100 100 0.1 0.04 1:0.4 38 24 0.1 0.008 1:0.08 0 0 0.02 1.0 1:50 100 100 0.02 0.2 1:10 100 100 0.02 0.04 1:2 54 24 0.02 0.008 1:0.4 0 0 0.004 5.0 1:1250 100 100 0.004 1.0 1:250 61 54 0.004 0.2 1:50 0 0 0.004 0.04 1:10 0 0 0.0008 5.0 1:6250 99 100 0.0008 1.0 1:1250 72 54 0.0008 0.2 1:250 0 0 0.0008 0.04 1:50 0 0 0.004 20.0 1:5000 100 100 0.004 4.0 1:1000 100 71 0.004 0.8 1:200 8 3 0.004 0.16 1:40 13 7 0.0008 20.0 1:25000 100 100 0.0008 4.0 1:5000 97 71 0.0008 0.8 1:1000 19 3 0.0008 0.16 1:200 22 7 0.02 5.0 1:250 98 100 0.02 1.0 1:50 100 100 0.02 0.2 1:10 58 12 0.02 0.04 1:2 19 16

TABLE I5 in vitro-Test with Ustilago segetum var. avenae (5.003) (5.010) (5.012) Colby (I-302) captan dithianon folpet Efficacy expected (ppm) (ppm) (ppm) (ppm) Ratio % value % 0.1 0 0.02 0 0.004 0 0.0008 0 20.0 100 4.0 100 0.8 0 0.16 0 20.0 99 4.0 100 0.8 8 10.0 100 2.0 100 0.4 15 0.08 4 0.1 20.0 1:200 100 100 0.1 4.0 1:40 100 100 0.1 0.8 1:8 10 0 0.1 0.16 1:1.6 7 0 0.02 20.0 1:1000 100 100 0.02 4.0 1:200 100 100 0.02 0.8 1:40 0 0 0.02 0.16 1:8 10 0 0.1 20.0 1:200 100 99 0.1 4.0 1:40 100 100 0.1 0.8 1:8 93 8 0.02 20.0 1:1000 100 99 0.02 4.0 1:200 100 100 0.02 0.8 1:40 15 8 0.0008 20.0 1:25000 100 99 0.0008 4.0 1:5000 100 100 0.0008 0.8 1:1000 10 8 0.1 10.0 1:100 100 100 0.1 2.0 1:20 100 100 0.1 0.4 1:4 25 15 0.1 0.08 1:0.8 12 4 0.004 10.0 1:2500 100 100 0.004 2.0 1:500 100 100 0.004 0.4 1:100 36 15 0.004 0.08 1:20 0 4 0.0008 10.0 1:12500 100 100 0.0008 2.0 1:2500 100 100 0.0008 0.4 1:500 27 15 0.0008 0.08 1:100 10 4

TABLE I6 in vitro-Test with Ustilago segetum var. avenae (3.012) (1.062) (1.055) (13.001) fluoxa- fluoxytio- (2.038) mefen- Colby (I-339) (1.067) fludioxonil strobin conazole isoflucypram trifluconazole Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 0 0.2 0 0.04 0 0.008 2 0.08 100 0.016 55 5 100 0.2 93 0.04 55 0.08 16 0.016 13 0.2 100 0.04 35 0.008 8 0.2 100 0.04 5 0.008 2 1 100 0.2 53 0.2 0.08 1:0.4 100 100 0.2 0.016 1:0.08 79 55 0.04 0.08 1:2 100 100 0.04 0.016 1:0.4 62 55 1 5 1:5 100 100 1 0.2 1:0.2 99 93 1 0.04 1:0.04 62 55 0.2 5 1:25 100 100 0.04 0.2 1:5 96 93 0.04 0.04 1:1 60 55 0.008 5 1:625 100 100 0.008 0.2 1:25 98 93 0.008 0.04 1:5 56 57 1 0.08 1:0.08 27 16 1 0.016 1:0.016 16 13 0.008 0.08 1:10 24 18 0.008 0.016 1:2 18 15 1 0.2 1:0.2 100 100 1 0.04 1:0.04 44 35 1 0.008 1:0.008 6 8 0.2 0.2 1:1 100 100 0.2 0.04 1:0.2 38 35 0.2 0.008 1:0.04 14 8 0.04 0.2 1:5 100 100 0.04 0.04 1:1 46 35 0.04 0.008 1:0.2 8 8 1 0.2 1:0.2 100 100 1 0.04 1:0.04 19 5 1 0.008 1:0.008 4 2 0.2 0.2 1:1 100 100 0.2 0.04 1:0.2 17 5 0.2 0.008 1:0.04 7 2 0.04 0.2 1:5 100 100 0.04 0.04 1:1 27 5 0.04 0.008 1:0.2 6 2 0.008 0.2 1:25 100 100 0.008 0.04 1:5 20 6 0.008 0.008 1:1 0 3 0.2 1 1:5 100 100 0.2 0.2 1:1 58 53 0.04 1 1:25 100 100 0.04 0.2 1:5 59 53 0.008 1 1:125 100 100 0.008 0.2 1:25 73 53

TABLE I7 in vitro-Test with Ustilago segetum var. avenae (12.004) (3.030) meta- metyl- (7.005) (1.020) (3.020) Colby (I-339) laxyl-m tetraprole pyrimethanil spiroxamin trifloxystrobin Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 0 0.2 0 0.04 0 0.008 2 20 12 4 8 0.8 11 1 34 4 42 0.8 18 0.16 12 20 74 0.2 54 0.04 38 1 20 1:20 12 12 1 4 1:4 18 8 1 0.8 1:0.8 15 11 0.008 20 1:2500 12 12 0.008 4 1:500 18 8 0.008 0.8 1:100 19 11 0.2 1 1:5 42 34 0.04 1 1:25 39 34 0.008 1 1:125 46 37 1 4 1:4 53 42 1 0.8 1:0.8 51 18 1 0.16 1:0.16 45 12 0.008 4 1:500 42 42 0.008 0.8 1:100 40 18 0.008 0.16 1:20 42 12 1 20 1:20 100 74 0.2 20 1:100 100 74 0.04 20 1:500 100 74 0.2 0.2 1:1 55 54 0.2 0.04 1:0.2 39 38 0.04 0.2 1:5 52 54 0.04 0.04 1:1 45 38

TABLE I8 in vitro-Test with Ustilago segetum var. avenae (2.002) (5.003) (1.002) (5.010) (3.025) Colby (I-338) (17.001) bixafen captan difenoconazole dithianon fenpicoxamid Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 0 0.2 0 0.04 0 0.008 0 1.6 0 0.2 44 1 28 0.2 100 0.04 40 0.008 2 2 29 0.4 0 0.08 2 0.2 1 0.04 6 0.008 14 0.2 1.6 1:8 6 0 0.04 1.6 1:40 12 0 0.008 1.6 1:200 5 1 0.2 0.2 1:1 67 44 0.04 0.2 1:5 57 44 0.008 0.2 1:25 64 44 0.2 1 1:5 32 28 0.04 1 1:25 30 28 0.008 1 1:125 36 28 0.04 0.2 1:5 100 100 0.04 0.04 1:1 42 41 0.04 0.008 1:0.2 13 3 0.008 0.2 1:25 99 100 0.008 0.04 1:5 42 40 0.008 0.008 1:1 9 2 0.2 2 1:10 39 29 0.2 0.4 1:2 5 0 0.2 0.08 1:0.4 3 2 0.04 2 1:50 36 30 0.04 0.4 1:10 2 1 0.04 0.08 1:2 4 3 1 0.2 1:0.2 5 1 1 0.04 1:0.04 11 6 1 0.008 1:0.008 17 14 0.2 0.2 1:1 13 1 0.2 0.04 1:0.2 7 6 0.2 0.008 1:0.04 14 14 0.04 0.2 1:5 11 2 0.04 0.04 1:1 12 7 0.04 0.008 1:0.2 14 15

TABLE I9 in vitro-Test with Ustilago segetum var. avenae (2.005) (3.012) (1.062) (5.012) (15.012) (2.038) Colby (I-338) fluopyram fluoxastrobin fluoxytioconazole folpet fosetylal isoflucypram Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 0 0.2 0 0.04 0 0.008 0 20 20 0.4 51 0.08 18 0.04 43 1 6 20 0 0.8 2 0.2 100 0.04 17 0.008 9 1 20 1:20  32 20 0.04 20 1:500 19 20 0.008 20  1:2500 21 20 1 0.4 1:0.4  52 51 1 0.08  1:0.08 24 18 0.2 0.4 1:2   51 51 0.2 0.08 1:0.4  22 18 0.04 0.4 1:10  51 51 0.04 0.08 1:2   20 18 0.008 0.4 1:50  50 51 0.008 0.08 1:10  29 18 1 0.04  1:0.04 48 43 0.04 0.04 1:1   57 43 0.008 0.04 1:5   43 43 1 1 1:1   41 26 0.2 1 1:5   19 6 0.04 1 1:25  16 6 0.008 1 1:125 20 6 0.2 20 1:100 15 0 0.2 0.8 1:4   25 2 0.04 20 1:500 10 0 0.04 0.8 1:20  8 2 0.008 20  1:2500 11 0 0.008 0.8 1:100 4 2 0.04 0.2 1:5   100 100 0.04 0.04 1:1   28 17 0.008 0.2 1:25  100 100 0.008 0.04 1:5   13 17

TABLE I10 in vitro-Test with Ustilago segetum var. avenae (1.055) (17.012) mefentri- (12.004) (15.016) (3.030) Paenibacillus (5.018) Colby (I-338) fluconazole metalaxylm metrafenone metyltetraprole terrae propineb Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 0 0.2 0 0.04 0 0.008 0 1 100 0.2 41 0.04 3 0.008 4 100 3 0.8 8 0.2 0 0.04 4 1 21 0.2 0 40 82 1.6 3 20 22 1 1 1:1   100 100 1 0.2 1:0.2  53 41 1 0.04  1:0.04 5 3 1 0.008   1:0.008 18 4 0.2 1 1:5   100 100 0.2 0.2 1:1   52 41 0.2 0.04 1:0.2  6 3 0.2 0.008  1:0.04 14 4 0.04 1 1:25  100 100 0.04 0.2 1:5   55 41 0.04 0.04 1:1   9 3 0.04 0.008 1:0.2  11 4 0.008 1 1:125 100 100 0.008 0.2 1:25  45 41 0.008 0.04 1:5   13 3 0.008 0.008 1:1   0 4 1 100 1:100 14 3 1 0.8 1:0.8  13 8 0.2 100 1:500 9 3 0.2 0.8 1:4   14 8 0.2 0.2 1:1   11 0 0.2 0.04 1:0.2  14 4 0.008 0.2 1:25  19 0 0.008 0.04 1:5   13 4 1 1 1:1   39 21 1 0.2 1:0.2  0 0 0.2 1 1:5   29 21 0.2 0.2 1:1   0 0 0.04 1 1:25  33 21 0.04 0.2 1:5   0 0 0.008 1 1:125 25 21 0.008 0.2 1:25  11 0 0.2 40 1:200 85 82 0.2 1.6 1:8   13 3 0.04 40  1:1000 95 82 0.04 1.6 1:40  11 3 0.008 40  1:5000 96 82 0.008 1.6 1:200 15 3 1 20 1:20  59 22 0.2 20 1:100 47 22 0.04 20 1:500 65 22 0.008 20  1:2500 28 22

TABLE I11 in vitro-Test with Ustilago segetum var. avenae (3.020) (17.012) (7.005) (13.005) (1.020) trifloxy Paenibacillus (5.018) Colby (I-338) pyrimethanil quinoxyfen spiroxamin strobin (I-130) terrae propineb Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 0 0.2 0 0.04 0 0.008 0 20 49 4 24 0.8 16 0.16 16 10 9 2 0 0.08 0 20 100 0.8 0 0.16 0 1 60 0.2 50 1 16 0.2 0 0.04 0 0.008 0 200 100 40 57 1.6 0 100 92 1 4 1:4   38 24 1 0.8 1:0.8  18 16 1 0.16  1:0.16 31 16 0.2 20 1:100 66 49 0.2 4 1:20  32 24 0.2 0.8 1:4   21 16 0.2 0.16 1:0.8  17 16 0.04 4 1:100 35 24 0.04 0.8 1:20  22 16 0.04 0.16 1:4   25 16 1 10 1:10  35 9 1 2 1:2   4 0 1 0.08  1:0.08 6 0 0.2 10 1:50  22 9 0.2 2 01:10   15 0 0.2 0.08 1:0.4  100 0 0.04 10 1:250 31 9 0.04 2 1:50  20 0 0.04 0.08 1:2   100 0 0.008 10  1:1250 23 9 0.008 2 1:250 7 0 1 20 1:20  100 100 1 0.8 1:0.8  12 0 1 0.16  1:0.16 0 0 0.04 20 1:500 100 100 0.04 0.8 1:20  0 0 0.04 0.16 1:4   6 0 1 1 1:1   64 60 1 0.2 1:0.2  54 50 0.2 1 1:5   62 60 0.2 0.2 1:1   52 50 0.008 1 1:125 65 60 0.008 0.2 1:25  58 50 0.04 200  1:5000 100 100 0.04 40  1:1000 90 57 0.04 1.6 1:40  0 0 0.008 200   1:25000 100 100 0.008 40  1:5000 57 57 0.008 1.6 1:200 0 0 1 100 1:100 95 93 0.2 100 1:500 95 92 0.04 100  1:2500 95 92

TABLE J1 in vitro-Test with Colletotrichum coccodes (13.005) (1.020) (1.021) (3.020) (2.002) Colby (I-339) quinoxyfen spiroxamin tebuconazole trifloxystrobin (1.067) bixafen Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 100 0.2 100 0.04 100 0.008 86 2 48 0.4 0 0.08 0 20 0 4 0 0.8 0 0.16 49 0.2 4 0.04 0 0.04 35 2 99 0.4 0 1 0 0.2 0 0.04 45 0.008 33 0.008 2 1:250 89 93 0.008 0.4 1:50  95 86 0.008 0.08 1:10  92 86 0.008 20  1:2500 89 86 0.008 4 1:500 96 86 0.008 0.8 1:100 100 86 0.008 0.16 1:20  100 93 0.04 0.2 1:5   100 100 0.04 0.04 1:1   100 100 0.008 0.2 1:25  86 87 0.008 0.04 1:5   98 86 1 0.04  1:0.04 100 100 0.2 0.04 1:0.2  98 100 0.008 0.04 1:5   98 91 0.2 2 1:10  100 100 0.2 0.4 1:2   100 100 0.008 2 1:250 100 100 0.008 0.4 1:50  53 40 0.008 1 1:125 64 40 0.008 0.2 1:25  78 40 0.008 0.04 1:5   68 67 0.008 0.008 1:1   66 60

TABLE J2 in vitro-Test with Colletotrichum coccodes (5.003) (1.002) (13.001) (2.005) (15.043) (3.012) Colby (I-339) captan difenoconazole fludioxonil fluopyram fluoxapiprolin fluoxa¬strobin Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 100 0.2 100 0.04 100 0.008 86 0.2 0 0.2 0.31 0.04 5 100 1 100 0.04 54 4 14 0.16 30 20 0 0.8 0 0.08 41 0.016 28 1 0.2 1:0.2  100 100 0.2 0.2 1:1   100 100 0.008 0.2 1:25  47 40 0.2 0.2 1:1   100 100 0.2 0.04 1:0.2  100 100 0.008 0.2 1:25  83 69 0.008 0.04 1:5   86 78 0.008 5 1:625 100 100 0.008 1 1:125 100 100 0.008 0.04 1:5   94 86 0.04 4 1:100 100 100 0.04 0.16 1:4   100 100 0.008 4 1:500 79 68 0.008 0.16 1:20  79 74 0.04 20 1:500 100 100 0.04 0.8 1:20  100 100 0.008 20  1:2500 78 63 0.008 0.8 1:100 67 63 0.2 0.08 1:0.4  100 100 0.2 0.016  1:0.08 100 100 0.008 0.08 1:10  100 79 0.008 0.016 1:2   100 74

TABLE J3 in vitro-Test with Colletotrichum coccodes (1.062) (1.055) fluoxy- (5.012) (15.012) (2.028) (2.038) mefentri- Colby (I-339) tioconazole folpet fosetylal inpyrfluxam isoflucypram fluconazole Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 100 0.2 100 0.04 100 0.008 86 0.04 0 0.008 32 1 66 0.04 3 0.008 1 20 0 4 0 0.8 0 1 4 0.2 57 0.04 19 0.008 52 1 0 0.2 8 0.04 46 0.008 0 1 100 0.2 34 0.008 0 0.04 0.04 1:1   100 100 0.04 0.008 1:0.2  100 100 0.008 0.04 1:5   80 63 0.008 0.008 1:1   96 75 0.008 1 1:125 100 78 0.008 0.04 1:5   40 37 0.008 0.008 1:1   62 36 0.008 20  1:2500 34 35 0.008 4 1:500 44 35 0.008 0.8 1:100 58 35 0.008 1 1:125 42 38 0.008 0.2 1:25  97 72 0.008 0.04 1:5   83 48 0.008 0.008 1:1   99 69 0.008 1 1:125 65 35 0.008 0.2 1:25  95 40 0.008 0.04 1:5   64 65 0.008 0.008 1:1   64 35 0.008 1 1:125 100 100 0.008 0.2 1:25  73 63 0.008 0.008 1:1   63 44

TABLE J4 in vitro-Test with Colletotrichum coccodes (17.012) (12.004) (15.016) (3.030) Paenibacillus (2.017) Colby (I-339) metalaxylm metrafenone metyltetraprole terrae penflufen Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 100 0.2 100 0.04 100 0.008 86 100 61 20 48 4 24 0.8 40 5 2 1 29 0.2 14 0.04 3 0.008 25 200 100 40 52 8 0 1.6 0 1 0 0.2 22 0.04 17 0.008 100  1:12500 100 78 0.008 20 1:2500 95 71 0.008 4 1:500  93 57 0.008 0.8 1:100  94 66 0.008 5 1:625  99 86 0.008 1 1:125  100 90 0.008 0.2 1:25   100 87 0.008 0.04 1:5    90 86 0.2 0.008 1:0.04  100 100 0.04 0.008 1:0.2   99 100 0.008 0.008 1:1    99 89 0.008 200  1:25000 100 100 0.008 40 1:5000 96 93 0.008 8 1:1000 100 85 0.008 1.6 1:200  99 85 0.008 1 1:125  100 85 0.008 0.2 1:25   100 89 0.008 0.04 1:5    100 88

TABLE J5 in vitro-Test with Colletotrichum coccodes (2.002) (5.003) (1.002) (5.010) Colby (I-338) (17.001) (1.067) bixafen captan difenoconazole dithianon Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 68 0.2 0 0.04 0 0.008 0 200 0 40 11 8 0 1.6 0 2 97 0.4 12 0.08 1 0.016 0 0.008 30 5 100 1 0 0.2 0 0.04 53 1 24 2 24 0.4 11 0.2 200 1:1000 70 0 0.2 40 1:200  21 11 0.2 8 1:40   3 0 0.04 200 1:5000 49 0 0.04 1.6 1:40   3 0 0.008 200  1:25000 9 0 0.008 40 1:5000 40 11 0.008 8 1:1000 23 0 0.008 1.6 1:200  12 0 0.2 2 1:10   100 97 0.2 0.4 1:2    51 12 0.2 0.08 1:0.4   22 1 0.2 0.016 1:0.08  56 0 0.04 2 1:50   100 97 0.04 0.4 1:10   16 12 0.04 0.08 1:2    3 1 0.04 0.016 1:0.4   69 0 1 0.008  1:0.008 98 78 0.04 0.008 1:0.2   50 31 0.008 0.008 1:1    38 30 1 5 1:5    100 100 1 1 1:1    100 68 1 0.2 1:0.2   99 68 1 0.04 1:0.04  99 85 0.2 5 1:25   100 100 0.2 1 1:5    100 0 0.2 0.2 1:1    56 0 0.04 5 1:125  100 100 0.04 1 1:25   100 0 0.04 0.2 1:5    34 0 0.008 5 1:625  100 100 0.008 1 1:125  86 0 0.008 0.2 1:25   0 0 0.2 1 1:5    27 25 0.04 1 1:25   23 24 0.008 1 1:125  84 24 0.2 2 1:10   48 25 0.2 0.4 1:2    26 12 0.008 2 1:250  100 24 0.008 0.4 1:50   15 11

TABLE J6 in vitro-Test with Colletotrichum coccodes (3.025) (13.001) (2.005) (15.043) (3.012) (15.012) Colby (I-338) fenpicoxamid fludioxonil fluopyram fluoxapiprolin fluoxastrobin fosetylal Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 53 0.2 1 0.04 0 0.008 0 1 16 0.2 23 0.04 21 0.008 25 0.04 74 4 0 0.8 0 0.16 0 20 0 4 0 0.16 0 2 0 0.08 0 0.016 0 100 15 20 2 4 0 0.8 27 1 1 1:1    99 61 1 0.2 1:0.2   87 64 1 0.04 1:0.04  92 63 1 0.008  1:0.008 90 65 0.04 1 1:25   48 16 0.04 0.2 1:5    68 23 0.04 0.04 1:1    20 21 0.008 1 1:125  48 16 0.008 0.2 1:25   31 23 0.008 0.04 1:5    49 21 1 0.04 1:0.04  99 88 0.2 0.04 1:0.2   76 75 0.04 0.04 1:1    73 74 0.008 4 1:500  71 0 0.008 0.8 1:100  13 0 0.008 0.16 1:20   2 0 0.008 20 1:2500 16 0 0.008 4 1:500  16 0 0.008 0.16 1:20   0 0 0.04 2 1:50   27 0 0.04 0.08 1:2    82 0 0.04 0.016 1:0.4   52 0 0.008 2 1:250  55 0 0.008 0.08 1:10   45 0 0.008 0.016 1:2    0 0 1 20 1:20   85 52 1 0.8 1:0.8   80 65 0.008 100  1:12500 72 27 0.008 20 1:2500 72 16 0.008 4 1:500  37 14

TABLE J7 in vitro-Test with Colletotrichum coccodes (1.055) (2.028) (2.038) (6.002) (5.013) mefentri- (15.016) Colby (I-338) inpyrfluxam isoflucypram isotianil mancozeb fluconazole metrafenone Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 51 0.2 51 0.04 12 0.008 14 1 10 0.2 0 0.04 14 0.008 58 1 0 0.2 0 0.04 0 0.008 34 100 0 20 0 20 100 4 0 0.8 0 0.16 0 0.2 22 1 4 0.2 2 0.04 0 1 1 1:1    57 56 1 0.2 1:0.2   78 51 1 0.04 1:0.04  99 58 1 0.008  1:0.008 82 80 1 0.2 1:0.2   91 51 1 0.04 1:0.04  96 51 1 0.008  1:0.008 100 68 0.2 1 1:5    55 51 0.2 0.2 1:1    95 51 0.04 0.2 1:5    18 12 0.04 0.04 1:1    48 12 0.008 1 1:125  50 14 0.008 0.2 1:25   48 14 0.2 100 1:500  39 19 0.2 20 1:100  46 19 0.04 100 1:2500 20 0 0.04 20 1:500  0 0 0.2 20 1:100  100 100 0.2 4 1:20   43 19 0.2 0.16 1:0.8   26 19 0.04 20 1:500  100 100 0.04 4 1:100  52 0 0.04 0.8 1:20   44 0 0.04 0.16 1:4    0 0 0.2 0.2 1:1    40 36 0.04 0.2 1:5    53 22 0.008 0.2 1:25   48 22 1 1 1:1    50 51 1 0.2 1:0.2   52 50 1 0.04 1:0.04  55 49 0.008 1 1:125  7 4 0.008 0.2 1:25   13 3 0.008 0.04 1:5    0 0

TABLE J8 in vitro-Test with Colletotrichum coccodes (17.012) (3.030) Paenibacillus (2.017) (5.018) (13.005) Colby (I-338) metyltetraprole terrae penflufen propineb quinoxyfen Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 49 0.2 12 0.04 1 0.008 0 0.2 1 0.04 0 0.008 0 200 100 40 19 8 0 1.6 0 5 27 1 0 0.2 0 0.04 0 20 31 10 28 2 18 0.4 0 1 0.2 1:0.2  91 50 1 0.04  1:0.04 56 49 1 0.008   1:0.008 90 49 0.008 0.04 1:5   21 0 0.008 0.008 1:1   44 0 0.2 200  1:1000 100 100 0.2 40 1:200 43 29 0.2 8 1:40  40 12 0.2 1.6 1:8   15 12 0.2 5 1:25  58 36 0.2 1 1:5   63 12 0.2 0.2 1:1   61 12 0.2 0.04 1:0.2  56 12 0.2 20 1:100 99 82 0.04 20 1:500 100 31 0.008 20  1:2500 100 31 0.04 10 1:250 62 59 0.04 2 1:50  60 53 0.04 0.4 1:10  43 43 0.008 10  1:1250 37 28 0.008 2 1:250 21 19 0.008 0.4 1:50  2 1

TABLE J9 in vitro-Test with Colletotrichum coccodes (1.021) (3.020) (5.010) (3.025) (15.043) Colby (I-338) tebuconazole trifloxystrobin (I-130) dithianon fenpicoxamid fluoxapiprolin Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 86 0.2 49 0.04 43 0.008 1 1 87 0.04 7 0.008 0 1 50 0.008 0 1 100 0.2 100 0.04 100 0.008 96 10 100 2 7 0.08 0 0.2 33 0.04 2 0.008 0 20 26 4 2 1.6 0 0.04 1 1:25  98 92 0.04 0.008 1:0.2  56 43 0.008 0.04 1:5   24 8 0.008 0.008 1:1   20 1 0.04 1 1:25  75 71 0.04 0.008 1:0.2  82 43 0.008 1 1:125 60 50 0.008 0.008 1:1   0 1 0.008 10  1:1250 100 100 0.008 2 1:250 100 96 0.008 0.08 1:10  100 96 0.008 0.2 1:25  100 97 0.008 0.04 1:5   100 96 0.008 0.008 1:1   100 96 0.008 20  1:2500 100 98 0.008 4 1:500 98 97 0.008 1.6 1:20  100 97

TABLE J10 in vitro-Test with Colletotrichum coccodes (1.062) (2.038) (13.004) (1.018) (7.005) (13.005) Colby (I-130) fluoxytioconazole isoflucypram proquinazid prothioconazole pyrimethanil quinoxyfen Efficacy expected (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) Ratio % value % 1 100 0.2 100 0.04 100 0.008 94 1 35 0.2 29 0.04 2 0.008 0 1 44 0.2 11 0.04 1 0.008 9 10 0 2 0 0.4 0 0.5 100 0.02 1 0.004 0 0.8 25 0.16 26 10 19 2 16 0.4 0 0.08 0 0.008 1 1:125 99 98 0.008 0.2 1:25  100 97 0.008 0.04 1:5   100 97 0.008 0.008 1:1   100 96 0.008 1 1:125 98 98 0.008 0.2 1:25  100 97 0.008 0.04 1:5   100 96 0.008 0.008 1:1   100 97 0.008 10  1:1250 97 97 0.008 2 1:250 100 97 0.008 0.4 1:50  100 97 0.008 0.5  1:62.5 100 100 0.008 0.02 1:2.5  99 97 0.008 0.004 1:0.5  99 97 0.008 0.8 1:20  100 100 0.008 0.16 1:4   100 100 0.008 0.8 1:100 100 98 0.008 0.16 1:20  99 98 0.008 10  1:1250 100 96 0.008 2 1:250 100 95 0.008 0.4 1:50  100 94 0.008 0.08 1:10  100 94

TABLE J11 in vitro -Test with Colletotrichum coccodes (1.020) (1.021) Colby (I-130) spiroxamin tebuconazole Efficacy expected (ppm) (ppm) (ppm) Ratio % value % 1 100 0.2 100 0.04 100 0.008 94 20 39 0.8 0 0.16 0 0.2 0 0.04 0 0.008 0 0.008 20 1:2500 100 97 0.008 0.8 1:100 100 94 0.008 0.16 1:20 98 94 0.008 0.2 1:25 97 94 0.008 0.04 1:5 98 94 0.008 0.008 1:1 99 94 

1. An active compound combination comprising (A) at least one compound of formula (I)

wherein A is selected from the group consisting of O, S, C(═O), S(═O), S(═O)₂, NR¹ and CR¹R², with R¹ and R² being independently selected from the group consisting of hydrogen, C₁-C₆-alkyl and C₃-C₈-cycloalkyl, or R¹ and R² form, together with the carbon atom to which they are attached to, a C₃-C₈-cycloalkyl or a non-aromatic 3- to 7-membered monocyclic heterocycle; m is 0, 1 or 2; T is selected from the group consisting of hydrogen, hydroxyl, C₁-C₆-alkyl, —C(═O)R^(a1), —C(═O)(OR^(a1)), —C(═O)N(R^(a2))₂, —S(═O)R^(a1), —S(═O)₂R^(a1) and S(═O)₂N(R^(a2))₂, with R^(a1) being selected from the group consisting of C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₃-C₈-cycloalkyl and C₂-C₆-alkenyl, with R^(a2) being independently selected from the group consisting of hydrogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₃-C₈-cycloalkyl and C₂-C₆-alkenyl; R³ and R⁴ are independently selected from the group consisting of hydrogen, halogen, cyano, hydroxyl, formyl, carboxyl, C₁-C₆-alkyl, C₁-C₆-alkoxy, C₁-C₆-alkylcarbonyl, C₁-C₆-alkoxycarbonyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl, C₃-C₈-cycloalkyl, aromatic C₆-C₁₄-carbocycle, aromatic 5- to 14-membered heterocycle, non-aromatic 3- to 14-membered heterocycle and —O—Si(C₁-C₆-alkyl)₃, or R³ and R⁴ form, together with the carbon atom to which they are attached to, a carbonyl, a methylidene, a C₃-C₈-cycloalkyl or a non-aromatic 3- to 7-membered monocyclic heterocycle; R⁵ is selected from the group consisting of hydrogen, hydroxyl, C₁-C₆-alkyl, C₁-C₆-alkoxy, C₁-C₆-alkylcarbonyloxy, C₁-C₆-alkylsulfanyl, C₁-C₆-alkylsulfinyl, C₁-C₆-alkylsulfonyl, C₃-C₈-cycloalkyl and —O—Si(C₁-C₆-alkyl)₃; wherein aliphatic R¹, R², R³, R⁴ and R⁵ substituents may be substituted with one or more substituents independently selected from the group consisting of halogen, cyano, amino, nitro, hydroxyl, formyl, carboxyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₁-C₆-alkoxycarbonyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, —O—Si(C₁-C₆-alkyl)₃ and non-aromatic 3- to 7-membered monocyclic heterocycle; wherein cyclic R¹, R², R³, R⁴ and R⁵ substituents may be substituted with one or more substituents independently selected from the group consisting of halogen, cyano, nitro, hydroxyl, formyl, oxo, methylidene, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₂-C₆-alkenyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, —O—Si(C₁-C₆-alkyl)₃ and non-aromatic 3- to 7-membered monocyclic heterocycle; R³ or R⁴, and R⁵ may form, together with the carbon atom to which they are attached to, a C₃-C₈-cycloalkyl; L represents a direct bond or L is selected from the group consisting of carbonyl, C₁-C₆-alkylene, C₁-C₆-alkylene substituted on a same carbon atom by two substituents forming together with the carbon atom to which they are attached to a C₃-C₈-cycloalkyl, C₁-C₆-alkylene substituted on a same carbon atom by two substituents forming together with the carbon atom to which they are attached to a non-aromatic 3- to 7-membered monocyclic heterocycle, C₂-C₆-alkenylene, C₂-C₆-alkynylene, C₃-C₈-cycloalkylene, C₁-C₆-alkylene-C₃-C₈-cycloalkylene, C₃-C₈-cycloalkylene-C₁-C₆-alkylene, C₁-C₆-alkylene-C₃-C₈-cycloalkylene-C₁-C₆-alkylene, C₁-C₆-alkylene-(C═O), C(═O)—C₁-C₆-alkylene, C₃-C₈-cycloalkenylene, C₁-C₆-alkylene-C₃-C₈-cycloalkenylene, C₃-C₈-cycloalkenylene-C₁-C₆-alkylene, C₁-C₆-alkylene-C₃-C₈-cycloalkenylene-C₁-C₆-alkylene, non-aromatic 3- to 7-membered monocyclic heterocyclylene, —NR^(aL1)—, —NR^(aL1)(C═O)—, —C(═O)NR^(aL1)—, —NR^(aL1)S(═O)₂—, —S(═O)₂NR^(aL1)—, —C(═NOR^(aL2))—, —C(═N—N(R^(aL2))₂) and —C(═NR^(aL2))—; with R^(aL1) being selected from the group consisting of hydrogen and C₁-C₆-alkyl, with R^(aL2) being independently selected from the group consisting of hydrogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₃-C₈-cycloalkyl and C₂-C₆-alkylenyl, wherein aliphatic L substituents may be substituted with one or more L^(Sa) substituents that may be the same or different wherein cyclic or cyclic moiety of L substituents may be substituted with one or more L^(Sc) substituents that may be the same or different, L^(sa) is selected from the group consisting of halogen, cyano, hydroxyl, carboxyl, methylidene, halomethylidene, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, C₁-C₆-alkoxycarbonyl, —O—Si(C₁-C₆-alkyl)₃ and non-aromatic 3- to 7-membered monocyclic heterocycle, L^(Sc) is selected from the group consisting of halogen, cyano, nitro, hydroxyl, formyl, carboxyl, oxo, methylidene, halomethylidene, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₂-C₆-alkenyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, —O—Si(C₁-C₆-alkyl)₃ and non-aromatic 3- to 7-membered monocyclic heterocycle, and/or two L^(Sc) substituents form, together with the carbon atom to which they are attached to, a C₃-C₈-cycloalkyl; R⁶ is selected from the group consisting of non-aromatic C₃-C₁₂-carbocycle, aromatic C₆-C₁₄-carbocycle, non-aromatic 3- to 14-membered heterocycle, aromatic 5- to 14-membered heterocycle, non-aromatic C₃-C₁₂-carbocyclyloxy, aromatic C₆-C₁₄-carbocyclyloxy, aromatic 5- to 14-membered heterocyclyloxy, non-aromatic 5- to 14-membered heterocyclyloxy, non-aromatic C₃-C₁₂-carbocyclylsulfanyl, aromatic C₆-C₁₄-carbocyclylsulfanyl, aromatic 5- to 14-membered heterocyclylsulfanyl, non-aromatic 5- to 14-membered heterocyclylsulfanyl, non-aromatic C₃-C₁₂-carbocyclylsulfinyl, aromatic C₆-C₁₄-carbocyclylsulfinyl, aromatic 5- to 14-membered heterocyclylsulfinyl, non-aromatic 5- to 14-membered heterocyclylsulfinyl, non-aromatic C₃-C₁₂-carbocyclylsulfonyl, aromatic C₆-C₁₄-carbocyclylsulfonyl, aromatic 5- to 14-membered heterocyclylsulfonyl, non-aromatic 5- to 14-membered heterocyclylsulfonyl, C₁-C₃-alkoxy substituted by a non-aromatic C₃-C₁₂-carbocycle, C₁-C₃-alkoxy substituted by an aromatic C₆-C₁₄-carbocycle, C₁-C₃-alkoxy substituted by a non-aromatic 3- to 14-membered heterocycle, C₁-C₃-alkoxy substituted by an aromatic 5- to 14-membered heterocycle, C₁-C₃-haloalkoxy substituted by a non-aromatic C₃-C₁₂-carbocycle, C₁-C₃-haloalkoxy substituted by an aromatic C₆-C₁₄-carbocycle, C₁-C₃-haloalkoxy substituted by a non-aromatic 3- to 14-membered heterocycle, C₁-C₃-haloalkoxy substituted by an aromatic 5- to 14-membered heterocycle, C₁-C₃-sulfanyl substituted by a non-aromatic C₃-C₁₂-carbocycle, C₁-C₃-sulfanyl substituted by an aromatic C₆-C₁₄-carbocycle, C₁-C₃-sulfanyl substituted by a non-aromatic 3- to 14-membered heterocycle and C₁-C₃-sulfanyl substituted by an aromatic 5- to 14-membered heterocycle, C₁-C₃-sulfinyl substituted by a non-aromatic C₃-C₁₂-carbocycle, C₁-C₃-sulfinyl substituted by an aromatic C₆-C₁₄-carbocycle, C₁-C₃-sulfinyl substituted by a non-aromatic 3- to 14-membered heterocycle and C₁-C₃-sulfinyl substituted by an aromatic 5- to 14-membered heterocycle, C₁-C₃-sulfonyl substituted by a non-aromatic C₃-C₁₂-carbocycle, C₁-C₃-sulfonyl substituted by an aromatic C₆-C₁₄-carbocycle, C₁-C₃-sulfonyl substituted by a non-aromatic 3- to 14-membered heterocycle and C₁-C₃-sulfonyl substituted by an aromatic 5- to 14-membered heterocycle; wherein cyclic, or cyclic moiety of, R⁶ substituents may be substituted with one or more R^(6S) substituents that may be the same or different, R^(6S) is selected from the group consisting of halogen, cyano, isocyano, nitro, hydroxyl, mercapto, pentafluorosulfanyl, oxo, methylidene, halomethylidene, formyl, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl, C₂-C₆-alkenyloxy, C₂-C₆-haloalkenyloxy, C₂-C₆-alkylnyloxy, C₂-C₆-haloalkylnyloxy, C₁-C₆-alkylsulfanyl, C₁-C₆-haloalkylsulfanyl, C₃-C₈-cycloalkylsulfanyl, C₁-C₆-alkylsulfinyl, C₁-C₆-haloalkylsulfinyl, C₃-C₈-cycloalkylsulfinyl, C₁-C₆-alkylsulfonyl, C₁-C₆-haloalkylsulfonyl, C₃-C₈-cycloalkylsulfonyl, C₃-C₈-cycloalkyl, C₃-C₈-cycloalkyloxy, C₃-C₈-cycloalkenyl, aromatic C₆-C₁₄-carbocycle, aromatic 5- or 6-membered monocyclic heterocycle, non-aromatic 3- to 7-membered monocyclic heterocycle, —N(R^(c))₂, —O—(C═O)R^(d), —C(═O)R^(d), —C(═O)(OR^(d)), —C(═O)N(R^(d))₂, —S(═O)₂N(R^(d))₂, —O—Si(C₁-C₆-alkyl)₃ and —Si(C₁-C₆-alkyl)₃, or two R^(6S) substituents may form, together with the carbon atom to which they are attached to, a C₃-C₈-cycloalkyl, with R^(c) being independently selected from the group consisting of hydrogen, C₁-C₆-alkyl and C₃-C₈-cycloalkyl, with R^(d) being independently selected from the group consisting of hydrogen, C₁-C₆-alkyl and C₁-C₆-haloalkyl, wherein aliphatic R^(6S), R^(c) and R^(d) substituents may be substituted with one or more substituents independently selected from the group consisting of cyano, halogen, hydroxyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, —O—Si(C₁-C₆-alkyl)₃, —Si(C₁-C₆-alkyl)₃, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl and non-aromatic 3- to 7-membered monocyclic heterocycle, wherein cyclic or cyclic moiety of R^(6S) and cyclic R^(e) substituents may be substituted with one or more substituents independently selected from the group consisting of halogen, cyano, nitro, hydroxyl, formyl, carboxyl, oxo, methylidene, halomethylidene, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₁-C₆-alkoxycarbonyl, C₁-C₆-haloalkoxycarbonyl, C₂-C₆-alkenyl, C₃-C₈-cycloalkyl and C₃-C₈-halocycloalkyl, and/or cyclic or cyclic moiety of R^(6S) substituents may be substituted with two substituents forming, together with the carbon atom to which they are attached to, a C₃-C₈-cycloalkyl; R⁷ is selected from the group consisting of hydrogen, halogen, cyano, isocyano, hydroxyl, mercapto, nitro, amino, formyl, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-hydroxyalkyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₁-C₆-alkylcarbonyl, C₁-C₆-haloalkylcarbonyl, C₁-C₆-alkoxycarbonyl, C₁-C₆-haloalkoxycarbonyl, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl, C₂-C₆-alkenyloxy, C₂-C₆-haloalkenyloxy, C₂-C₆-alkynyloxy, C₂-C₆-haloalkynyloxy, C₁-C₆-alkylsulfanyl, C₁-C₆-haloalkylsulfanyl, C₃-C₈-cycloalkylsulfanyl, C₂-C₆-alkenylsulfanyl, C₂-C₆-alkynylsulfanyl, C₁-C₆-alkylsulfinyl, C₁-C₆-haloalkylsulfinyl, C₃-C₈-cycloalkylsulfinyl, C₁-C₆-alkylsulfonyl, C₁-C₆-haloalkylsulfonyl, C₃-C₈-cycloalkylsulfonyl, C₃-C₈-cycloalkyl, C₃-C₆-cycloalkenyl, aromatic C₆-C₁₄-carbocycle, aromatic 5- or 6-membered monocyclic heterocycle, non-aromatic 3- to 7-membered monocyclic heterocycle, C₃-C₈-cycloalkyloxy, aromatic C₆-C₁₄-carbocyclyloxy, aromatic 5- or 6-membered monocyclic heterocyclyloxy, non-aromatic 3- to 7-membered monocyclic heterocyclyloxy, —O—Si(C₁-C₆-alkyl)₃, —Si(C₁-C₆-alkyl)₃, —N(R^(e))₂, —C(═NR^(f))R^(f), NR^(g)C(═O)R^(g), —C(═O)(OR^(g)), —C(═O)N(R^(g))₂, —S(═O)₂N(R^(g))₂ and —S(═O)(═NR^(g))R^(g), with R^(e) being independently selected from the group consisting of hydrogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, aromatic C₆-C₁₄-carbocycle, aromatic 5- or 6-membered monocyclic heterocycle and non-aromatic 3- to 7-membered monocyclic heterocycle, with R^(f) being independently selected from the group consisting of hydroxyl, amino, cyano, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy, C₁-C₆-alkylamino and di(C₁-C₆-alkyl)amino, with R^(g) being independently selected from the group consisting of hydrogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl and C₃-C₈-cycloalkyl, wherein aliphatic R⁷, R^(e), R^(f) and R^(g) substituents may be substituted with one or more R^(7Sa) substituents that may be the same or different, wherein cyclic or cyclic moiety of R⁷, cyclic R^(e) and cyclic R^(g) substituents may be substituted with one or more R^(7Sc) substituents that may be the same or different, R^(7Sa) is selected from the group consisting of cyano, hydroxyl, carboxyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, C₁-C₆-alkoxycarbonyl, —O—Si(C₁-C₆-alkyl)₃, —Si(C₁-C₆-alkyl)₃, aromatic C₆-C₁₄-carbocycle and non-aromatic 3- to 7-membered monocyclic heterocycle, R^(7Sc) is selected from the group consisting of halogen, cyano, nitro, hydroxyl, formyl, oxo, methylidene, halomethylidene, C₁-C₆-alkyl, C₁-C₆-haloalkyl C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₂-C₆-alkenyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, —O—Si(C₁-C₆-alkyl)₃ and non-aromatic 3- to 7-membered monocyclic heterocycle, or two R^(7Sc) substituents form, together with the carbon atom to which they are attached to, a C₃-C₈-cycloalkyl; R⁸ is selected from the group consisting of hydrogen, halogen, cyano, isocyano, amino, nitro, hydroxyl, mercapto, carboxyl, C₁-C₆-alkoxycarbonyl, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-hydroxyalkyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl, C₂-C₆-alkenyloxy, C₂-C₆-haloalkenyloxy, C₂-C₆-alkynyloxy, C₂-C₆-haloalkynyloxy, C₃-C₈-cycloalkyl, C₃-C₆-cycloalkenyl, aromatic C₆-C₁₄-carbocycle, non-aromatic 3- to 14-membered heterocycle, aromatic 5- to 14-membered heterocycle, C₃-C₈-cycloalkyloxy, aromatic C₆-C₁₄-carbocyclyloxy, non-aromatic 3- to 14-membered heterocyclyloxy, aromatic 5- to 14-membered heterocyclyloxy, —O—Si(C₁-C₆-alkyl)₃, —Si(C₁-C₆-alkyl)₃, —N(R^(h))₂, —SR^(i), —S(═O)R^(i) and —S(═O)₂R^(i), with R^(h) being independently selected from the group consisting of hydrogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, aromatic C₆-C₁₄-carbocycle, aromatic 5- to 14-membered heterocycle and non-aromatic 3- to 7-membered monocyclic heterocycle, with R^(i) being selected from the group consisting of C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, aromatic C₆-C₁₄-carbocycle, aromatic 5- to 14-membered heterocycle and non-aromatic 3- to 7-membered monocyclic heterocycle, wherein aliphatic R⁸, R^(h) and R^(i) substituents may be substituted with one or more R^(8Sa) substituents that may be the same or different, wherein cyclic or cyclic moiety of R⁸, cyclic R^(h) and cyclic R^(i) substituents may be substituted with one or more R^(8Sc) substituents that may be the same or different, R^(8Sa) is selected from the group consisting of cyano, amino, nitro, hydroxyl, formyl, carboxyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₁-C₆-alkoxy-C₁-C₆-alkoxy, C₁-C₆-alkoxycarbonyl, C₁-C₆-haloalkoxycarbonyl, C₁-C₆-alkylcarbonyl, C₁-C₆-haloalkylcarbonyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, C₁-C₆-alkylsulfanyl, C₁-C₆-haloalkylsulfanyl, C₁-C₆-alkylsulfinyl, C₁-C₆-haloalkylsulfinyl, C₁-C₆-alkylsulfonyl, C₁-C₆-haloalkylsulfonyl, —O—Si(C₁-C₆-alkyl)₃, —Si(C₁-C₆-alkyl)₃, non-aromatic 3- to 7-membered monocyclic heterocycle and —N(R^(a′))₂ with R^(a′) being independently selected from the group consisting of hydrogen, formyl, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₃-C₈-cycloalkyl and C₁-C₆-alkylcarbonyl, wherein said non-aromatic 3- to 7-membered monocyclic heterocycle R^(8Sa) may be substituted with one or more C₁-C₆-alkyl substituents that may be the same or different, R^(8Sc) is selected from the group consisting of halogen, cyano, amino, nitro, hydroxyl, formyl, carboxyl, oxo, methylidene, halomethylidene, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₁-C₆-alkoxycarbonyl, C₁-C₆-haloalkoxycarbonyl, C₂-C₆-alkenyl, C₁-C₆-alkylsulfanyl, C₁-C₆-alkylsulfinyl, C₁-C₆-alkylsulfonyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, —O—Si(C₁-C₆-alkyl)₃ and non-aromatic 3- to 7-membered monocyclic heterocycle that may be substituted with one or more C₁-C₆-alkyl substituents that may be the same or different, or two R^(8Sc) substituents form, together with the carbon atom to which they are attached to, a C₃-C₈-cycloalkyl or a non-aromatic 3- to 7-membered monocyclic heterocycle, wherein said non-aromatic 3- to 7-membered monocyclic heterocycle may be substituted with one or more C₁-C₆-alkyl substituents that may be the same or different; Q is selected from the group consisting of aromatic C₆-C₁₄-carbocycle, non-aromatic C₃-C₁₂-carbocycle, non-aromatic 3- to 14-membered heterocycle and aromatic 5- to 14-membered heterocycle, wherein any of said carbocycle or heterocycle groups may be substituted with one or more Q^(S) substituents that may be the same or different, Q^(S) is selected from the group consisting of halogen, cyano, isocyano, nitro, hydroxyl, mercapto, formyl, carboxyl, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkylcarbonyl, C₁-C₆-haloalkylcarbonyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₁-C₆-alkoxycarbonyl, C₁-C₆-haloalkoxycarbonyl, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl, C₂-C₆-alkenyloxy, C₂-C₆-haloalkenyloxy, C₁-C₆-alkylsulfanyl, C₁-C₆-haloalkylsulfanyl, C₁-C₆-alkylsulfinyl, C₁-C₆-haloalkylsulfinyl, C₁-C₆-alkylsulfonyl, C₁-C₆-haloalkylsulfonyl, C₃-C₈-cycloalkyl, C₃-C₈-cycloalkyloxy, C₃-C₆-cycloalkenyl, non-aromatic 3- to 7-membered monocyclic heterocycle, aromatic C₆-C₁₄-carbocycle, aromatic 5- to 14-membered heterocycle, —O—Si(C₁-C₆-alkyl)₃, —Si(C₁-C₆-alkyl)₃, —O—C(═O)R^(j), —NR^(j)C(═O)R^(j), —C(═O)N(R^(j))₂, —C(═S)R^(j), —C(═S)N(R^(j))₂, —C(═NR^(j))R^(j) and —C(═NOR^(j))R^(j) and —N(R^(k))₂ with R^(j) being independently selected from the group consisting of hydrogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl and C₁-C₆-alkoxy, with R^(k) being independently selected from the group consisting of hydrogen, hydroxyl, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl and C₃-C₈-cycloalkyl, wherein aliphatic Q^(S), R^(j) and R^(k) substituents may be substituted with one or more substituents independently selected from the group consisting of cyano, amino, nitro, hydroxyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₁-C₆-alkoxycarbonyl, C₁-C₆-haloalkoxycarbonyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, —Si(C₁-C₆-alkyl)₃ and non-aromatic 3- to 7-membered monocyclic heterocycle, wherein cyclic or cyclic moiety of Q^(S) and cyclic R^(k) substituents may be substituted with one or more R^(Qs) substituents independently selected from the group consisting of halogen, cyano, amino, nitro, hydroxyl, formyl, carboxyl, oxo, methylidene, halomethylidene, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₁-C₆-alkoxycarbonyl, C₁-C₆-haloalkoxycarbonyl, C₃-C₈-cycloalkyl, C₃-C₈-halocycloalkyl, C₂-C₆-alkenyl and non-aromatic 3- to 7-membered monocyclic heterocycle, wherein cyclic R^(Qs) substituents may be substituted with two substituents forming, together with the carbon atom to which they are attached to, a C₃-C₈-cycloalkyl, and (B) at least one further active compound selected from the group consisting of (1) inhibitors of the ergosterol synthesis, (2) inhibitors of the respiratory chain at complex I or II, (3) inhibitors of the respiratory chain at complex III, (4) inhibitors of the mitosis and cell division, (5) compounds capable of having a multisite action, (6) compounds capable of inducing a host defense, (7) inhibitors of the amino acid and/or protein biosynthesis, (8) inhibitors of the ATP production, (9) inhibitors of the cell wall synthesis, (10) inhibitors of the lipid and membrane synthesis, (11) inhibitors of the melanine biosynthesis, (12) inhibitors of the nucleic acid synthesis, (13) inhibitors of the signal transduction, (14) compounds capable of acting as uncoupler, (15) other fungicides, (16) antibacterial agents, (17) biological fungicides and (18) fatty acids or derivatives thereof.
 2. The active compound combination according to claim 1, wherein the compound of formula (I) is a compound of formula (I) wherein A is selected from the group consisting of O, S, C(═O), S(═O), S(═O)₂, NR¹ and CR¹R², with R¹ and R² being independently selected from the group consisting of hydrogen, C₁-C₄-alkyl and C₃-C₆-cycloalkyl, m is 0, 1 or 2; T is selected from the group consisting of hydrogen and C₁-C₄-alkyl, R³ and R⁴ are independently selected from the group consisting of hydrogen, fluorine, chlorine, C₁-C₄-alkyl, C₂-C₄-alkenyl, C₂-C₄-alkynyl, C₃-C₆-cycloalkyl, R⁵ is selected from the group consisting of hydrogen, hydroxyl, C₁-C₄-alkyl, C₁-C₄-alkoxy, C₁-C₄-alkylsulfanyl, wherein aliphatic R¹, R², R³, R⁴ and R⁵ substituents may be substituted with one to three substituents independently selected from the group consisting of fluorine, chlorine, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₃-C₆-cycloalkyl, C₃-C₆-halocycloalkyl, wherein cyclic R¹, R², R³, R⁴ and R⁵ substituents may be substituted with one to three substituents independently selected from the group consisting of fluorine, chlorine oxo, methylidene, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₂-C₄-alkenyl, C₃-C₆-cycloalkyl, C₃-C₆-halocycloalkyl, R³ or R⁴, and R⁵ may form, together with the carbon atom to which they are attached to, a C₃-C₆-cycloalkyl; L represents a direct bond or L is selected from the group consisting of C₁-C₆-alkylene, C₁-C₆-alkylene substituted on a same carbon atom by two substituents forming together with the carbon atom to which they are attached to a C₃-C₆-cycloalkyl, C₁-C₆-alkylene substituted on a same carbon atom by two substituents forming together with the carbon atom to which they are attached to a non-aromatic 3- to 7-membered monocyclic heterocycle, wherein aliphatic L substituents may be substituted with one to three L^(Sa) substituents independently selected from the group consisting of fluorine, chlorine, hydroxyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₃-C₆-cycloalkyl and C₃-C₆-halocycloalkyl, wherein cyclic or cyclic moiety of L substituents may be substituted with one to three L^(Sc) substituents independently selected from the group consisting of fluorine, chlorine, hydroxyl, oxo, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₂-C₄-alkenyl, C₃-C₆-cycloalkyl and C₃-C₆-halocycloalkyl, R⁶ is selected from the group consisting of non-aromatic C₃-C₁₂-carbocycle, aromatic C₆-C₁₄-carbocycle, non-aromatic 3- to 14-membered heterocycle, aromatic 5- to 14-membered heterocycle, non-aromatic C₃-C₁₂-carbocyclyloxy, aromatic C₆-C₁₄-carbocyclyloxy, aromatic 5- to 14-membered heterocyclyloxy, non-aromatic 5- to 14-membered heterocyclyloxy, non-aromatic C₃-C₁₂-carbocyclylsulfanyl, aromatic C₆-C₁₄-carbocyclylsulfanyl, aromatic 5- to 14-membered heterocyclylsulfanyl and non-aromatic 5- to 14-membered heterocyclylsulfanyl, wherein cyclic, or cyclic moiety of, R⁶ substituents may be substituted with one to three R^(6S) substituents that may be the same or different, R^(6S) is selected from the group consisting of halogen, cyano, nitro, hydroxyl, mercapto, pentafluorosulfanyl, oxo, methylidene, halomethylidene, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl, C₁-C₆-alkylsulfanyl, C₁-C₆-haloalkylsulfanyl, C₃-C₆-cycloalkylsulfanyl, C₃-C₆-cycloalkyl, C₃-C₆-cycloalkyloxy, phenyl, naphthyl aromatic 5- or 6-membered monocyclic heterocycle, non-aromatic 3- to 7-membered monocyclic heterocycle, —C(═O)(OR^(d)) and —C(═O)N(R^(d))₂, with R^(d) being independently selected from the group consisting of hydrogen, C₁-C₄-alkyl and C₁-C₄-haloalkyl, wherein aliphatic R^(6S), R^(c) and R^(d) substituents may be substituted with one to three substituents independently selected from the group consisting of fluorine, chlorine hydroxyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₃-C₆-cycloalkyl and C₃-C₆-halocycloalkyl, wherein cyclic or cyclic moiety of R^(6S) and cyclic R^(c) substituents may be substituted with one to three substituents independently selected from the group consisting of fluorine, chlorine C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy and C₁-C₄-haloalkoxy, R⁷ is selected from the group consisting of hydrogen, halogen, cyano, hydroxyl, mercapto, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-hydroxyalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₁-C₄-alkylcarbonyl, C₁-C₄-haloalkylcarbonyl, C₂-C₄-alkenyl, C₂-C₄-haloalkenyl, C₂-C₄-alkynyl, C₂-C₄-haloalkynyl, C₁-C₄-alkylsulfanyl, C₁-C₄-haloalkylsulfanyl, C₃-C₆-cycloalkylsulfanyl, C₁-C₄-alkylsulfinyl, C₁-C₄-haloalkylsulfinyl, C₃-C₆-cycloalkylsulfinyl, C₁-C₄-alkylsulfonyl, C₁-C₄-haloalkylsulfonyl, C₃-C₆-cycloalkylsulfonyl, C₃-C₆-cycloalkyl, C₃-C₆-cycloalkenyl, phenyl, naphthyl, aromatic 5- or 6-membered monocyclic heterocycle, non-aromatic 3- to 7-membered monocyclic heterocycle, C₃-C₈-cycloalkyloxy, aromatic C₆-C₁₄-carbocyclyloxy, aromatic 5- or 6-membered monocyclic heterocyclyloxy, non-aromatic 3- to 7-membered monocyclic heterocyclyloxy, —N(R^(e))₂, —C(═NR^(f))R^(f), NR^(g)C(═O)R^(g), —C(═O)(OR^(g)), —C(═O)N(R^(g))₂, —S(═O)₂N(R^(g))₂ and —S(═O)(═NR^(g))R^(g), with R^(e) being independently selected from the group consisting of hydrogen, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₂-C₄-alkenyl, C₂-C₄-haloalkenyl, C₂-C₄-alkynyl, C₂-C₄-haloalkynyl, C₃-C₆-cycloalkyl, C₃-C₆-halocycloalkyl, with R^(f) being independently selected from the group consisting of hydroxyl, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, with R^(g) being independently selected from the group consisting of hydrogen, C₁-C₄-alkyl, C₁-C₄-haloalkyl and C₃-C₆-cycloalkyl, wherein aliphatic R⁷, R^(e), R^(f) and R^(g) substituents may be substituted with one to three R^(7Sa) substituents that may be the same or different, wherein cyclic or cyclic moiety of R⁷, cyclic R^(e) and cyclic R^(g) substituents may be substituted with one to three R^(7Sc) substituents that may be the same or different, R^(7Sa) is selected from the group consisting of hydroxyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₃-C₆-cycloalkyl, R^(7Sc) is selected from the group consisting of fluorine, chlorine hydroxyl, oxo, C₁-C₄-alkyl, C₁-C₄-haloalkyl C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₃-C₆-cycloalkyl, R⁸ is selected from the group consisting of hydrogen, halogen, amino, hydroxyl, mercapto, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-hydroxyalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₂-C₄-alkenyl, C₂-C₄-haloalkenyl, C₂-C₄-alkynyl, C₂-C₄-haloalkynyl, C₂-C₄-alkenyloxy, C₂-C₄-haloalkenyloxy, C₂-C₄-alkynyloxy, C₂-C₄-haloalkynyloxy, C₃-C₆-cycloalkyl, C₃-C₆-cycloalkenyl, phenyl, naphthyl, non-aromatic 3- to 7-membered heterocycle, aromatic 5- or 6-membered heterocycle, C₃-C₆-cycloalkyloxy, phenyloxy, naphthyloxy, non-aromatic 3- to 7-membered heterocyclyloxy, aromatic 5- or 6-membered heterocyclyloxy, —N(R^(h))₂, —SR^(i), —S(═O)R^(i) and —S(═O)₂R^(i), with R^(h) being independently selected from the group consisting of hydrogen, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₂-C₄-alkenyl, C₂-C₄-haloalkenyl, C₃-C₆-cycloalkyl, C₃-C₆-halocycloalkyl, phenyl, naphthyl aromatic 5- or 6-membered heterocycle and non-aromatic 3- to 7-membered monocyclic heterocycle, with R^(i) being selected from the group consisting of C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₂-C₄-alkenyl, C₂-C₄-haloalkenyl, C₂-C₄-alkynyl, C₂-C₄-haloalkynyl, C₃-C₆-cycloalkyl, C₃-C₆-halocycloalkyl, phenyl, naphthyl, aromatic 5- or 6-membered heterocycle and non-aromatic 3- to 7-membered monocyclic heterocycle, wherein aliphatic R⁸, R^(h) and R^(i) substituents may be substituted with one to three R^(8Sa) substituents that may be the same or different, wherein cyclic or cyclic moiety of R⁸, cyclic R^(h) and cyclic R^(i) substituents may be substituted with one to three R^(8Sc) substituents that may be the same or different, R^(8Sa) is selected from the group consisting of hydroxyl, carboxyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₁-C₄-alkoxycarbonyl, C₁-C₄-haloalkoxycarbonyl, C₃-C₆-cycloalkyl, C₃-C₆-halocycloalkyl, C₁-C₄-alkylsulfanyl, C₁-C₄-haloalkylsulfanyl, C₁-C₄-alkylsulfinyl, C₁-C₄-haloalkylsulfinyl, C₁-C₄-alkylsulfonyl, C₁-C₄-haloalkylsulfonyl,—and non-aromatic 3- to 7-membered monocyclic heterocycle, wherein said non-aromatic 3- to 7-membered monocyclic heterocycle R^(8Sa) may be substituted with one or two C₁-C₄-alkyl substituents that may be the same or different, R^(8Sc) is selected from the group consisting of halogen, oxo, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy and C₃-C₆-cycloalkyl, Q is selected from the group consisting of phenyl, naphthyl, non-aromatic C₅-C₁₀-carbocycle, non-aromatic 5- to 10-membered heterocycle and aromatic 5- to 10-membered heterocycle, wherein any of said carbocycle or heterocycle groups may be substituted with one to three Q^(S) substituents that may be the same or different, Q^(S) is selected from the group consisting of halogen, cyano, nitro, formyl, carboxyl, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkylcarbonyl, C₁-C₄-haloalkylcarbonyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₁-C₄-alkoxycarbonyl, C₁-C₄-haloalkoxycarbonyl, C₂-C₄-alkenyl, C₂-C₄-haloalkenyl, C₂-C₄-alkynyl, C₂-C₄-haloalkynyl, C₁-C₄-alkylsulfanyl, C₁-C₄-haloalkylsulfanyl, C₁-C₄-alkylsulfinyl, C₁-C₄-haloalkylsulfinyl, C₁-C₄-alkylsulfonyl, C₁-C₄-haloalkylsulfonyl, C₃-C₆-cycloalkyl, non-aromatic 3- to 7-membered monocyclic heterocycle, phenyl, naphthyl and aromatic 5- to 10-membered heterocycle, wherein aliphatic Q^(S), R^(j) and R^(k) substituents may be substituted with one to three substituents independently selected from the group consisting of hydroxyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₃-C₆-cycloalkyl and C₃-C₆-halocycloalkyl, wherein cyclic or cyclic moiety of Q^(S) and cyclic R^(k) substituents may be substituted with one to three R^(Qs) substituents independently selected from the group consisting of fluorine, chlorine, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy and C₃-C₆-cycloalkyl.
 3. The active compound combination according to claim 1, wherein the compound of formula (I) is a compound of formula (I), wherein A is selected from the group consisting of O, NR¹ and CR¹R², with R¹ and R² being independently selected from the group consisting of hydrogen, methyl or ethyl, m is 1; T is hydrogen, R³ and R⁴ are independently selected from the group consisting of hydrogen or fluorine, R⁵ is hydrogen, L represents a direct bond or L is methylene, R⁶ is indanyl, 1,2,3,4-tetrahydronaphthalenyl, phenyl, naphthyl, 2,3-dihydrobenzofuranyl, 2,3-dihydro-1,4-benzodioxinyl, thienyl, pyridinyl, indolyl, benzofuranyl, benzothiophenyl or phenoxy, wherein cyclic, or cyclic moiety of R⁶ substituents may be substituted with one or two R^(6S) substituents that may be the same or different, R^(6S) is selected from the group consisting of halogen, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₂-C₄-alkenyl, C₂-C₄-alkynyl, C₁-C₄-haloalkylsulfanyl, C₃-C₅-cycloalkyl pyridinyl, oxetanyl and tetrahydrofuranyl R⁷ is selected from the group consisting of halogen, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-hydroxyalkyl, C₁-C₄-alkoxy, C₁-C₄-alkylcarbonyl, C₃-C₆-cycloalkyl, imidazolyl, pyrazolyl, thiazolyl and pyridinyl, wherein aliphatic R⁷, substituents may be substituted with one or two R^(7Sa) substituents independently selected from the group consisting of hydroxyl, methoxy, ethoxy and cyclopropyl, wherein cyclic or cyclic moiety of R⁷ substituents may be substituted with one or two R^(7Sc) substituents independently selected from the group consisting of fluorine, methyl, ethyl and cyclopropyl, R⁸ is selected from the group consisting of hydrogen, halogen, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₃-C₆-cycloalkyloxy and —N(R^(h))₂, with R^(h) being independently selected from the group consisting of hydrogen, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₂-C₄-alkenyl, and C₃-C₆-cycloalkyl, wherein aliphatic R⁸ and R^(h) substituents may be substituted with one or two R^(8Sa) substituents independently selected from the group consisting of hydroxyl, methoxy and ethoxy, wherein cyclic or cyclic moiety of R⁸ and cyclic R^(h) substituents may be substituted with one or two R^(8Sc) substituents independently selected from the group consisting of fluorine, methyl, ethyl and cyclopropyl, Q is selected from the group consisting of phenyl, 3-bicyclo[4.2.0]octa-1,3,5-trienyl, pyrazolyl, thiazolyl, thienyl and pyridinyl, wherein any of said carbocycle or heterocycle groups may be substituted with one to three Q^(S) substituents that may be the same or different, Q^(S) is selected from the group consisting of halogen, cyano, nitro, formyl, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₂-C₄-alkenyl, C₂-C₄-alkynyl, C₁-C₄-alkylsulfanyl C₃-C₅-cycloalkyl, oxiranyl and oxetanyl.
 4. The active compound combination according to claim 1, wherein the compound of formula (I) is a compound of formula (I), wherein A is O, m is 1; T is hydrogen, R³ and R⁴ are hydrogen, R⁵ is hydrogen, L is methylene, R⁶ is 2,4-dimethylphenyl, 2-methyl-4-bromophenyl or 2-chloro-4-methylphenyl, R⁷ is methyl, R⁸ is hydrogen, Q is 2-fluoro-3-chlorophenyl, 2-fluor-3-bromophenyl or 2-fluoro-3-cyclopropylphenyl.
 5. The active compound combination according to claim 1, wherein the compound of formula (I) selected from the group consisting of (I-052) rac-3-[3-(3-cyclopropyl-2-fluorophenoxy)-6-methylpyridazin-4-yl]-5-[(2,4-dimethylphenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazine, (I-130) (5S)-3-[3-(3-cyclopropyl-2-fluorophenoxy)-6-methylpyridazin-4-yl]-5-(2,4-dimethylbenzyl)-5,6-dihydro-4H-1,2,4-oxadiazine, (I-300) rac-5-[(4-bromo-2-methylphenyl)methyl]-3-[3-(3-chloro-2-fluorophenoxy)-6-methylpyridazin-4-yl]-5,6-dihydro-4H-1,2,4-oxadiazine, (I-302) rac-3-[3-(3-chloro-2-fluorophenoxy)-6-methylpyridazin-4-yl]-5-[(2-chloro-4-methylphenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazine, (I-337) (5S)-5-[(4-bromo-2-methylphenyl)methyl]-3-[3-(3-chloro-2-fluorophenoxy)-6-methylpyridazin-4-yl]-5,6-dihydro-4H-1,2,4-oxadiazine, (I-338) (5R)-3-[3-(3-chloro-2-fluorophenoxy)-6-methylpyridazin-4-yl]-5-(2-chloro-4-methylbenzyl)-5,6-dihydro-4H-1,2,4-oxadiazine and (I-339) (5S)-3-[3-(3-chloro-2-fluorophenoxy)-6-methylpyridazin-4-yl]-5-(2-chloro-4-methylbenzyl)-5,6-dihydro-4H-1,2,4-oxadiazine.
 6. The active compound combination according to claim 1, wherein the compound of formula (I) selected from the group consisting of (I-302) rac-3-[3-(3-chloro-2-fluorophenoxy)-6-methylpyridazin-4-yl]-5-[(2-chloro-4-methylphenyl)methyl]-5,6-dihydro-4H-1,2,4-oxadiazine, (I-338) (5R)-3-[3-(3-chloro-2-fluorophenoxy)-6-methylpyridazin-4-yl]-5-(2-chloro-4-methylbenzyl)-5,6-dihydro-4H-1,2,4-oxadiazine and (I-339) (5S)-3-[3-(3-chloro-2-fluorophenoxy)-6-methylpyridazin-4-yl]-5-(2-chloro-4-methylbenzyl)-5,6-dihydro-4H-1,2,4-oxadiazine.
 7. The active compound combination according to claim 1, wherein the further active compound is selected from the group consisting of inhibitors of the ergosterol biosynthesis selected from the group consisting of (1.001) cyproconazole, (1.002) difenoconazole, (1.003) epoxiconazole, (1.004) fenhexamid, (1.005) fenpropidin, (1.006) fenpropimorph, (1.007) fenpyrazamine, (1.008) fluquinconazole, (1.009) flutriafol, (1.010) imazalil, (1.011) imazalil sulfate, (1.012) ipconazole, (1.013) metconazole, (1.014) myclobutanil, (1.015) paclobutrazol, (1.016) prochloraz, (1.017) propiconazole, (1.018) prothioconazole, (1.019) pyrisoxazole, (1.020) spiroxamine, (1.021) tebuconazole, (1.022) tetraconazole, (1.023) triadimenol, (1.024) tridemorph, (1.025) triticonazole, (1.026) (1R,2S,5S)-5-(4-chlorobenzyl)-2-(chloromethyl)-2-methyl-1-(1H-1,2,4-triazol-1-ylmethyl)cyclopentanol, (1.027) (1S,2R,5R)-5-(4-chlorobenzyl)-2-(chloromethyl)-2-methyl-1-(1H-1,2,4-triazol-1-ylmethyl)cyclopentanol, (1.028) (2R)-2-(1-chlorocyclopropyl)-4-[(1R)-2,2-dichlorocyclopropyl]-1-(1H-1,2,4-triazol-1-yl)butan-2-ol, (1.029) (2R)-2-(1-chlorocyclopropyl)-4-[(1S)-2,2-dichlorocyclopropyl]-1-(1H-1,2,4-triazol-1-yl)butan-2-ol, (1.030) (2R)-2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1-(1H-1,2,4-triazol-1-yl)propan-2-ol, (1.031) (2S)-2-(1-chlorocyclopropyl)-4-[(1R)-2,2-dichlorocyclopropyl]-1-(1H-1,2,4-triazol-1-yl)butan-2-ol, (1.032) (2S)-2-(1-chlorocyclopropyl)-4-[(1S)-2,2-dichlorocyclopropyl]-1-(1H-1,2,4-triazol-1-yl)butan-2-ol, (1.033) (2S)-2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1-(1H-1,2,4-triazol-1-yl)propan-2-ol, (1.034) (R)-[3-(4-chloro-2-fluorophenyl)-5-(2,4-difluorophenyl)-1,2-oxazol-4-yl](pyridin-3-yl)methanol, (1.035) (S)-[3-(4-chloro-2-fluorophenyl)-5-(2,4-difluorophenyl)-1,2-oxazol-4-yl](pyridin-3-yl)methanol, (1.036) [3-(4-chloro-2-fluorophenyl)-5-(2,4-difluorophenyl)-1,2-oxazol-4-yl](pyridin-3-yl)methanol, (1.037) 1-({(2R,4S)-2-[2-chloro-4-(4-chlorophenoxy)phenyl]-4-methyl-1,3-dioxolan-2-yl}methyl)-1H-1,2,4-triazole, (1.038) 1-({(2S,4S)-2-[2-chloro-4-(4-chlorophenoxy)phenyl]-4-methyl-1,3-dioxolan-2-yl}methyl)-1H-1,2,4-triazole, (1.039) 1-{[3-(2-chlorophenyl)-2-(2,4-difluoro-phenyl)oxiran-2-yl]methyl}-1H-1,2,4-triazol-5-yl thiocyanate, (1.040) 1-{[rel(2R,3R)-3-(2-chlorophenyl)-2-(2,4-difluorophenyl)oxiran-2-yl]methyl}-1H-1,2,4-triazol-5-yl thiocyanate, (1.041) 1-{[rel(2R,3S)-3-(2-chlorophenyl)-2-(2,4-difluorophenyl)oxiran-2-yl]methyl}-1H-1,2,4-triazol-5-yl thiocyanate, (1.042) 2-[(2R,4R,5R)-1-(2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazole-3-thione, (1.043) 2-[(2R,4R,5S)-1-(2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazole-3-thione, (1.044) 2-[(2R,4S,5R)-1-(2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazole-3-thione, (1.045) 2-[(2R,4S,5S)-1-(2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazole-3-thione, (1.046) 2-[(2S,4R,5R)-1-(2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazole-3-thione, (1.047) 2-[(2S,4R,5S)-1-(2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazole-3-thione, (1.048) 2-[(2S,4S,5R)-1-(2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazole-3-thione, (1.049) 2-[(2S,4S,5S)-1-(2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazole-3-thione, (1.050) 2-[1-(2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazole-3-thione, (1.051) 2-[2-chloro-4-(2,4-dichlorophenoxy)phenyl]-1-(1H-1,2,4-triazol-1-yl)propan-2-ol, (1.052) 2-[2-chloro-4-(4-chlorophenoxy)phenyl]-1-(1H-1,2,4-triazol-1-yl)butan-2-ol, (1.053) 2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1-(1H-1,2,4-triazol-1-yl)butan-2-ol, (1.054) 2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1-(1H-1,2,4-triazol-1-yl)pentan-2-ol, (1.055) mefentrifluconazole, (1.056) 2-{[3-(2-chlorophenyl)-2-(2,4-difluorophenyl)oxiran-2-yl]methyl}-2,4-dihydro-3H-1,2,4-triazole-3-thione, (1.057) 2-{[rel(2R,3R)-3-(2-chlorophenyl)-2-(2,4-difluorophenyl)oxiran-2-yl]methyl}-2,4-dihydro-3H-1,2,4-triazole-3-thione, (1.058) 2-{[rel(2R,3S)-3-(2-chlorophenyl)-2-(2,4-difluoro-phenyl)oxiran-2-yl]methyl}-2,4-dihydro-3H-1,2,4-triazole-3-thione, (1.059) 5-(4-chloro-benzyl)-2-(chloromethyl)-2-methyl-1-(1H-1,2,4-triazol-1-ylmethyl)cyclopentanol, (1.060) 5-(allylsulfanyl)-1-{[3-(2-chlorophenyl)-2-(2,4-difluorophenyl)oxiran-2-yl]methyl}-1H-1,2,4-triazole, (1.061) 5-(allylsulfanyl)-1-{[rel(2R,3R)-3-(2-chlorophenyl)-2-(2,4-difluorophenyl)oxiran-2-yl]methyl}-1H-1,2,4-triazole, (1.062) 5-(allylsulfanyl)-1-{[rel(2R,3S)-3-(2-chlorophenyl)-2-(2,4-difluorophenyl)oxiran-2-yl]methyl}-1H-1,2,4-triazole, (1.063) N′-(2,5-dimethyl-4-{[3-(1,1,2,2-tetrafluoro-ethoxy)phenyl]sulfanyl}phenyl)-N-ethyl-N-methylimidoformamide, (1.064) N′-(2,5-dimethyl-4-{[3-(2,2,2-trifluoroethoxy)phenyl]sulfanyl}phenyl)N-ethyl-N-methylimidoformamide, (1.065) N′-(2,5-dimethyl-4-{[3-(2,2,3,3-tetrafluoro-propoxy)phenyl]sulfanyl}phenyl)-N-ethyl-N-methylimidoformamide, (1.066) N′-(2,5-dimethyl-4-{[3-(pentafluoroethoxy)phenyl]sulfanyl}phenyl)-N-ethyl-N-methylimidoformamide, (1.067) N′-(2,5-dimethyl-4-{3-[(1,1,2,2-tetrafluoroethyl)sulfanyl]-phenoxy}phenyl)-N-ethyl-N-methylimidoformamide, (1.068) N′-(2,5-dimethyl-4-{3-[(2,2,2-trifluoroethyl)sulfanyl]phenoxy}phenyl)-N-ethyl-N-methylimidoformamide, (1.069) N′-(2,5-dimethyl-4-{3-[(2,2,3,3-tetrafluoropropyl)sulfanyl]phenoxy}phenyl)-N-ethyl-N-methylimidoformamide, (1.070) N′-(2,5-dimethyl-4-{3-[(pentafluoro-ethyl)sulfanyl]phenoxy}phenyl)-N-ethyl-N-methylimidoformamide, (1.071) N′-(2,5-dimethyl-4-phenoxyphenyl)-N-ethyl-N-methylimidoformamide, (1.072) N′-(4-{[3-(difluoromethoxy)phenyl]sulfanyl}-2,5-dimethylphenyl)-N-ethyl-N-methylimidoformamide, (1.073) N′-(4-{3-[(difluoromethyl)sulfanyl]phenoxy}-2,5-dimethylphenyl)-N-ethyl-N-methylimidoformamide, (1.074) N′-[5-bromo-6-(2,3-dihydro-1H-inden-2-yloxy)-2-methylpyridin-3-yl]-N-ethyl-N-methylimidoformamide, (1.075) N′-{4-[(4,5-dichloro-1,3-thiazol-2-yl)oxy]-2,5-dimethylphenyl}-N-ethyl-N-methylimidoformamide, (1.076) N′-{5-bromo-6-[(1R)-1-(3,5-difluorophenyl)ethoxy]-2-methylpyridin-3-yl}-N-ethyl-N-methylimidoformamide, (1.077) N′-{5-bromo-6-[(1S)-1-(3,5-difluorophenyl)ethoxy]-2-methylpyridin-3-yl}-N-ethyl-N-methylimidoformamide, (1.078) N′-{5-bromo-6-[(cis-4-isopropylcyclohexyl)oxy]-2-methylpyridin-3-yl}-N-ethyl-N-methylimidoformamide, (1.079) N′-{5-bromo-6-[(trans-4-isopropylcyclohexyl)oxy]-2-methylpyridin-3-yl}-N-ethyl-N-methylimidoformamide, (1.080) N′-{5-bromo-6-[1-(3,5-difluorophenyl)ethoxy]-2-methylpyridin-3-yl}-N-ethyl-N-methylimidoformamide, (1.081) ipfentrifluconazole, (1.082) 2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1-(1H-1,2,4-triazol-1-yl)propan-2-ol, (1.083) 2-[6-(4-bromophenoxy)-2-(trifluoro-methyl)-3-pyridyl]-1-(1,2,4-triazol-1-yl)propan-2-ol, (1.084) 2-[6-(4-chlorophenoxy)-2-(trifluoromethyl)-3-pyridyl]-1-(1,2,4-triazol-1-yl)propan-2-ol, (1.085) 3-[2-(1-chlorocyclopropyl)-3-(3-chloro-2-fluoro-phenyl)-2-hydroxy-propyl]imidazole-4-carbonitrile, (1.086) 4-[[6-[rac-(2R)-2-(2,4-difluorophenyl)-1,1-difluoro-2-hydroxy-3-(5-thioxo-4H-1,2,4-triazol-1-yl)propyl]-3-pyridyl]oxy]benzonitrile, (1.087) N-isopropyl-N′-[5-methoxy-2-methyl-4-(2,2,2-trifluoro-1-hydroxy-1-phenylethyl)phenyl]-N-methylimidoformamide, (1.088) N′-{5-bromo-2-methyl-6-[(1-propoxypropan-2-yl)oxy]pyridin-3-yl}-N-ethyl-N-methylimidoformamide, (1.089) hexaconazole, (1.090) penconazole, (1.091) fenbuconazole, (1.092) methyl 2-[2-chloro-4-(4-chlorophenoxy)phenyl]-2-hydroxy-3-(1,2,4-triazol-1-yl)propanoate inhibitors of the respiratory chain at complex I or II selected from the group consisting of (2.001) benzovindiflupyr, (2.002) bixafen, (2.003) boscalid, (2.004) carboxin, (2.005) fluopyram, (2.006) flutolanil, (2.007) fluxapyroxad, (2.008) furametpyr, (2.009) Isofetamid, (2.010) isopyrazam (anti-epimeric enantiomer 1R,4S,9S), (2.011) isopyrazam (anti-epimeric enantiomer 1S,4R,9R), (2.012) isopyrazam (anti-epimeric racemate 1RS,4SR,9SR), (2.013) isopyrazam (mixture of syn-epimeric racemate 1RS,4SR,9RS and anti-epimeric racemate 1RS,4SR,9SR), (2.014) isopyrazam (syn-epimeric enantiomer 1R,4S,9R), (2.015) isopyrazam (syn-epimeric enantiomer 1S,4R,9S), (2.016) isopyrazam (syn-epimeric racemate 1RS,4SR,9RS), (2.017) penflufen, (2.018) penthiopyrad, (2.019) pydiflumetofen, (2.020) Pyraziflumid, (2.021) sedaxane, (2.022) 1,3-dimethyl-N-(1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl)-1H-pyrazole-4-carboxamide, (2.023) 1,3-dimethyl-N-[(3R)-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl]-1H-pyrazole-4-carboxamide, (2.024) 1,3-dimethyl-N-[(3S)-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl]-1H-pyrazole-4-carboxamide, (2.025) 1-methyl-3-(trifluoromethyl)-N-[2′-(trifluoromethyl)biphenyl-2-yl]-1H-pyrazole-4-carboxamide, (2.026) 2-fluoro-6-(trifluoromethyl)-N-(1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl)benzamide, (2.027) 3-(difluoromethyl)-1-methyl-N-(1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl)-1H-pyrazole-4-carboxamide, (2.028) inpyrfluxam, (2.029) 3-(difluoromethyl)-1-methyl-N-[(3S)-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl]-1H-pyrazole-4-carboxamide, (2.030) fluindapyr, (2.031) 3-(difluoromethyl)-N-[(3R)-7-fluoro-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl]-1-methyl-1H-pyrazole-4-carboxamide, (2.032) 3-(difluoromethyl)-N-[(3S)-7-fluoro-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl]-1-methyl-1H-pyrazole-4-carboxamide, (2.033) 5,8-difluoro-N-[2-(2-fluoro-4-{[4-(trifluoromethyl)pyridin-2-yl]oxy}phenyl)ethyl]quinazolin-4-amine, (2.034) N-(2-cyclopentyl-5-fluorobenzyl)-N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.035) N-(2-tert-butyl-5-methylbenzyl)-N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.036) N-(2-tert-butylbenzyl)-N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.037) N-(5-chloro-2-ethylbenzyl)-N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.038) isoflucypram, (2.039) N-[(1R,4S)-9-(dichloromethylene)-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl]-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide, (2.040) N-[(1S,4R)-9-(dichloromethylene)-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl]-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide, (2.041) N-[1-(2,4-dichlorophenyl)-1-methoxy-propan-2-yl]-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide, (2.042) N-[2-chloro-6-(trifluoromethyl)benzyl]-N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.043) N-[3-chloro-2-fluoro-6-(trifluoromethyl)benzyl]-N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.044) N-[5-chloro-2-(trifluoromethyl)benzyl]-N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.045) N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl-N-[5-methyl-2-(trifluoromethyl)benzyl]-1H-pyrazole-4-carboxamide, (2.046) N-cyclopropyl-3-(difluoromethyl)-5-fluoro-N-(2-fluoro-6-isopropylbenzyl)-1-methyl-1H-pyrazole-4-carboxamide, (2.047) N-cyclopropyl-3-(difluoromethyl)-5-fluoro-N-(2-isopropyl-5-methylbenzyl)-1-methyl-1H-pyrazole-4-carboxamide, (2.048) N-cyclopropyl-3-(difluoromethyl)-5-fluoro-N-(2-isopropylbenzyl)-1-methyl-1H-pyrazole-4-carbothioamide, (2.049) N-cyclopropyl-3-(difluoromethyl)-5-fluoro-N-(2-isopropylbenzyl)-1-methyl-1H-pyrazole-4-carboxamide, (2.050) N-cyclopropyl-3-(difluoromethyl)-5-fluoro-N-(5-fluoro-2-isopropylbenzyl)-1-methyl-1H-pyrazole-4-carboxamide, (2.051) N-cyclopropyl-3-(difluoromethyl)-N-(2-ethyl-4,5-dimethylbenzyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.052) N-cyclopropyl-3-(difluoromethyl)-N-(2-ethyl-5-fluorobenzyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.053) N-cyclopropyl-3-(difluoromethyl)-N-(2-ethyl-5-methylbenzyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.054) N-cyclopropyl-N-(2-cyclopropyl-5-fluorobenzyl)-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.055) N-cyclopropyl-N-(2-cyclopropyl-5-methylbenzyl)-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.056) N-cyclopropyl-N-(2-cyclopropylbenzyl)-3-(di-fluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.057) pyrapropoyne, (2.058) N-[rac-(1S,2S)-2-(2,4-dichlorophenyl)cyclobutyl]-2-(trifluoromethyl)-nicotinamide, (2.059) N-[(1S,2S)-2-(2,4-dichlorophenyl)cyclobutyl]-2-(trifluoromethyl)nicotinamide, (2.060) flubeneteram, inhibitors of the respiratory chain at complex III selected from the group consisting of (3.001) ametoctradin, (3.002) amisulbrom, (3.003) azoxystrobin, (3.004) coumethoxystrobin, (3.005) coumoxystrobin, (3.006) cyazofamid, (3.007) dimoxystrobin, (3.008) enoxastrobin, (3.009) famoxadone, (3.010) fenamidone, (3.011) flufenoxystrobin, (3.012) fluoxastrobin, (3.013) kresoxim-methyl, (3.014) metominostrobin, (3.015) orysastrobin, (3.016) picoxystrobin, (3.017) pyraclostrobin, (3.018) pyrametostrobin, (3.019) pyraoxystrobin, (3.020) trifloxystrobin, (3.021) (2E)-2-{2-[({[(1E)-1-(3-{[(E)-1-fluoro-2-phenylvinyl]oxy}phenyl)ethylidene]amino}oxy)methyl]phenyl}-2-(methoxyimino)-N-methylacetamide, (3.022) (2E,3Z)-5-{[1-(4-chlorophenyl)-1H-pyrazol-3-yl]oxy}-2-(methoxyimino)-N,3-dimethylpent-3-enamide, (3.023) (2R)-2-{2-[(2,5-dimethylphenoxy)methyl]phenyl}-2-methoxy-N-methylacetamide, (3.024) (2S)-2-{2-[(2,5-dimethylphenoxy)methyl]phenyl}-2-methoxy-N-methylacetamide, (3.025) fenpicoxamid, (3.026) mandestrobin, (3.027) N-(3-ethyl-3,5,5-trimethylcyclohexyl)-3-formamido-2-hydroxybenzamide, (3.028) (2E,3Z)-5-{[1-(4-chloro-2-fluorophenyl)-1H-pyrazol-3-yl]oxy}-2-(methoxyimino)-N,3-dimethylpent-3-enamide, (3.029) methyl {5-[3-(2,4-dimethylphenyl)-1H-pyrazol-1-yl]-2-methylbenzyl}carbamate, (3.030) metyltetraprole, (3.031) florylpicoxamid, (3.032) (2S,3S)-3-(o-tolyl)butan-2-yl N-{[4-methoxy-3-(propanoyloxy)-2-pyridyl]carbonyl}-L-alaninate, inhibitors of the mitosis and cell division selected from the group consisting of (4.001) carbendazim, (4.002) diethofencarb, (4.003) ethaboxam, (4.004) fluopicolide, (4.005) pencycuron, (4.006) thiabendazole, (4.007) thiophanate-methyl, (4.008) zoxamide, (4.009) pyridachlometyl, (4.010) 3-chloro-5-(4-chlorophenyl)-4-(2,6-difluorophenyl)-6-methylpyridazine, (4.011) 3-chloro-5-(6-chloropyridin-3-yl)-6-methyl-4-(2,4,6-trifluoro-phenyl)pyridazine, (4.012) 4-(2-bromo-4-fluorophenyl)-N-(2,6-difluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.013) 4-(2-bromo-4-fluorophenyl)-N-(2-bromo-6-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.014) 4-(2-bromo-4-fluorophenyl)-N-(2-bromophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.015) 4-(2-bromo-4-fluorophenyl)-N-(2-chloro-6-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.016) 4-(2-bromo-4-fluorophenyl)-N-(2-chlorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.017) 4-(2-bromo-4-fluorophenyl)-N-(2-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.018) 4-(2-chloro-4-fluorophenyl)-N-(2,6-difluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.019) 4-(2-chloro-4-fluorophenyl)-N-(2-chloro-6-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.020) 4-(2-chloro-4-fluorophenyl)-N-(2-chlorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.021) 4-(2-chloro-4-fluorophenyl)-N-(2-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.022) 4-(4-chlorophenyl)-5-(2,6-difluorophenyl)-3,6-dimethylpyridazine, (4.023) N-(2-bromo-6-fluorophenyl)-4-(2-chloro-4-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.024) N-(2-bromophenyl)-4-(2-chloro-4-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.025) N-(4-chloro-2,6-difluorophenyl)-4-(2-chloro-4-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.026) fluopimomide, compounds capable to have a multisite action selected from the group consisting of (5.001) bordeaux mixture, (5.002) captafol, (5.003) captan, (5.004) chlorothalonil, (5.005) copper hydroxide, (5.006) copper naphthenate, (5.007) copper oxide, (5.008) copper oxychloride, (5.009) copper(2+) sulfate, (5.010) dithianon, (5.011) dodine, (5.012) folpet, (5.013) mancozeb, (5.014) maneb, (5.015) metiram, (5.016) metiram zinc, (5.017) oxine-copper, (5.018) propineb, (5.019) sulfur and sulfur preparations including calcium polysulfide, (5.020) thiram, (5.021) zineb, (5.022) ziram, (5.023) 6-ethyl-5,7-dioxo-6,7-dihydro-5H-pyrrolo[3′,4′:5,6][1,4]dithiino[2,3-c][1,2]thiazole-3-carbonitrile, compounds capable to induce a host defence selected from the group consisting of (6.001) acibenzolar-S-methyl, (6.002) isotianil, (6.003) probenazole, (6.004) tiadinil, inhibitors of the amino acid and/or protein biosynthesis selected from the group consisting of (7.001) cyprodinil, (7.002) kasugamycin, (7.003) kasugamycin hydrochloride hydrate, (7.004) oxytetracycline, (7.005) pyrimethanil, (7.006) 3-(5-fluoro-3,3,4,4-tetramethyl-3,4-dihydroisoquinolin-1-yl)quinoline, inhibitors of the ATP production selected from the group consisting of (8.001) silthiofam, inhibitors of the cell wall synthesis selected from the group consisting of (9.001) benthiavalicarb, (9.002) dimethomorph, (9.003) flumorph, (9.004) iprovalicarb, (9.005) mandipropamid, (9.006) pyrimorph, (9.007) valifenalate, (9.008) (2E)-3-(4-tert-butylphenyl)-3-(2-chloropyridin-4-yl)-1-(morpholin-4-yl)prop-2-en-1-one, (9.009) (2Z)-3-(4-tert-butylphenyl)-3-(2-chloropyridin-4-yl)-1-(morpholin-4-yl)prop-2-en-1-one, inhibitors of the lipid and membrane synthesis selected from the group consisting of (10.001) propamocarb, (10.002) propamocarb hydrochloride, (10.003) tolclofos-methyl, inhibitors of the melanin biosynthesis selected from the group consisting of (11.001) tricyclazole, (11.002) tolprocarb, inhibitors of the nucleic acid synthesis selected from the group consisting of (12.001) benalaxyl, (12.002) benalaxyl-M (kiralaxyl), (12.003) metalaxyl, (12.004) metalaxyl-M (mefenoxam), inhibitors of the signal transduction selected from the group consisting of (13.001) fludioxonil, (13.002) iprodione, (13.003) procymidone, (13.004) proquinazid, (13.005) quinoxyfen, (13.006) vinclozolin, compounds capable to act as an uncoupler selected from the group consisting of (14.001) fluazinam, (14.002) meptyldinocap, further fungicides selected from the group consisting of (15.001) abscisic acid, (15.002) benthiazole, (15.003) bethoxazin, (15.004) capsimycin, (15.005) carvone, (15.006) chinomethionat, (15.007) cufraneb, (15.008) cyflufenamid, (15.009) cymoxanil, (15.010) cyprosulfamide, (15.011) flutianil, (15.012) fosetyl-aluminium, (15.013) fosetyl-calcium, (15.014) fosetyl-sodium, (15.015) methyl isothiocyanate, (15.016) metrafenone, (15.017) mildiomycin, (15.018) natamycin, (15.019) nickel dimethyldithiocarbamate, (15.020) nitrothal-isopropyl, (15.021) oxamocarb, (15.022) oxathiapiprolin, (15.023) oxyfenthiin, (15.024) pentachlorophenol and salts, (15.025) phosphorous acid and its salts, (15.026) propamocarb-fosetylate, (15.027) pyriofenone (chlazafenone), (15.028) tebufloquin, (15.029) tecloftalam, (15.030) tolnifanide, (15.031) 1-(4-{4-[(5R)-5-(2,6-difluorophenyl)-4,5-dihydro-1,2-oxazol-3-yl]-1,3-thiazol-2-yl}piperidin-1-yl)-2-[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]ethanone, (15.032) 1-(4-{4-[(5S)-5-(2,6-difluorophenyl)-4,5-dihydro-1,2-oxazol-3-yl]-1,3-thiazol-2-yl}piperidin-1-yl)-2-[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]ethanone, (15.033) 2-(6-benzylpyridin-2-yl)quinazoline, (15.034) dipymetitrone, (15.035) 2-[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]-1-[4-(4-{5-[2-(prop-2-yn-1-yloxy)phenyl]-4,5-dihydro-1,2-oxazol-3-yl}-1,3-thiazol-2-yl)piperidin-1-yl]ethanone, (15.036) 2-[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]-1-[4-(4-{5-[2-chloro-6-(prop-2-yn-1-yloxy)phenyl]-4,5-dihydro-1,2-oxazol-3-yl}-1,3-thiazol-2-yl)piperidin-1-yl]ethanone, (15.037) 2-[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]-1-[4-(4-{5-[2-fluoro-6-(prop-2-yn-1-yloxy)phenyl]-4,5-dihydro-1,2-oxazol-3-yl}-1,3-thiazol-2-yl)piperidin-1-yl]ethanone, (15.038) 2-[6-(3-fluoro-4-methoxyphenyl)-5-methylpyridin-2-yl]quinazoline, (15.039) 2-{(5R)-3-[2-(1-{[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4-yl]-4,5-dihydro-1,2-oxazol-5-yl}-3-chlorophenyl methanesulfonate, (15.040) 2-{(5S)-3-[2-(1-{[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4-yl]-4,5-dihydro-1,2-oxazol-5-yl}-3-chlorophenyl methanesulfonate, (15.041) ipflufenoquin, (15.042) 2-{2-fluoro-6-[(8-fluoro-2-methylquinolin-3-yl)oxy]phenyl}propan-2-ol, (15.043) fluoxapiprolin, (15.044) 2-{3-[2-(1-{[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4-yl]-4,5-dihydro-1,2-oxazol-5-yl}phenyl methanesulfonate, (15.045) 2-phenylphenol and salts, (15.046) 3-(4,4,5-trifluoro-3,3-dimethyl-3,4-dihydroisoquinolin-1-yl)quinoline, (15.047) quinofumelin, (15.048) 4-amino-5-fluoropyrimidin-2-ol (tautomeric form: 4-amino-5-fluoropyrimidin-2(1H)-one), (15.049) 4-oxo-4-[(2-phenylethyl)amino]butanoic acid, (15.050) 5-amino-1,3,4-thiadiazole-2-thiol, (15.051) 5-chloro-N′-phenyl-N′-(prop-2-yn-1-yl)thiophene-2-sulfonohydrazide, (15.052) 5-fluoro-2-[(4-fluorobenzyl)oxy]-pyrimidin-4-amine, (15.053) 5-fluoro-2-[(4-methylbenzyl)oxy]pyrimidin-4-amine, (15.054) 9-fluoro-2,2-dimethyl-5-(quinolin-3-yl)-2,3-dihydro-1,4-benzoxazepine, (15.055) but-3-yn-1-yl {6-[({[(Z)-(1-methyl-1H-tetrazol-5-yl)(phenyl)methylene]amino}oxy)methyl]pyridin-2-yl}carbamate, (15.056) ethyl (2Z)-3-amino-2-cyano-3-phenylacrylate, (15.057) phenazine-1-carboxylic acid, (15.058) propyl 3,4,5-trihydroxybenzoate, (15.059) quinolin-8-ol, (15.060) quinolin-8-ol sulfate (2:1), (15.061) tert-butyl {6-[({[(1-methyl-1H-tetrazol-5-yl)(phenyl)methylene]amino}oxy)methyl]pyridin-2-yl}carbamate, (15.062) 5-fluoro-4-imino-3-methyl-1-[(4-methylphenyl)sulfonyl]-3,4-dihydropyrimidin-2(1H)-one, (15.063) aminopyrifen, (15.064) (N′-[2-chloro-4-(2-fluorophenoxy)-5-methylphenyl]-N-ethyl-N-methylimidoformamide), (15.065) (N′-(2-chloro-5-methyl-4-phenoxyphenyl)-N-ethyl-N-methylimidoformamide), (15.066) (2-{2-[(7,8-difluoro-2-methylquinolin-3-yl)oxy]-6-fluorophenyl}propan-2-ol), (15.067) (5-bromo-1-(5,6-dimethylpyridin-3-yl)-3,3-dimethyl-3,4-dihydroisoquinoline), (15.068) (3-(4,4-difluoro-5,5-dimethyl-4,5-dihydrothieno[2,3-c]pyridin-7-yl)quinoline), (15.069) (1-(4,5-dimethyl-1H-benzimidazol-1-yl)-4,4-difluoro-3,3-dimethyl-3,4-dihydroisoquinoline), (15.070) 8-fluoro-3-(5-fluoro-3,3-dimethyl-3,4-dihydroisoquinolin-1-yl)quinolone, (15.071) 8-fluoro-3-(5-fluoro-3,3,4,4-tetramethyl-3,4-dihydroisoquinolin-1-yl)quinolone, (15.072) 3-(4,4-difluoro-3,3-dimethyl-3,4-dihydroisoquinolin-1-yl)-8-fluoroquinoline, (15.073) (N-methyl-N-phenyl-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide), (15.074) methyl {4-[5-(trifluoro-methyl)-1,2,4-oxadiazol-3-yl]phenyl}carbamate, (15.075) (N-{4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzyl}cyclopropanecarboxamide), (15.076) N-methyl-4-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide, (15.077) N-[(E)-methoxyiminomethyl]-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide, (15.078) N—[(Z)-methoxyiminomethyl]-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide, (15.079) N-[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]cyclopropanecarboxamide, (15.080) N-(2-fluorophenyl)-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide, (15.081) 2,2-difluoro-N-methyl-2-[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]-acetamide, (15.082) N-allyl-N-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)phenyl]methyl]acetamide, (15.083) N-[(E)-N-methoxy-C-methyl-carbonimidoyl]-4-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide, (15.084) N—[(Z)—N-methoxy-C-methyl-carbonimidoyl]-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide, (15.085) N-allyl-N-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]propanamide, (15.086) 4,4-dimethyl-1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]-pyrrolidin-2-one, (15.087) N-methyl-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]-benzenecarbothioamide, (15.088) 5-methyl-1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]pyrrolidin-2-one, (15.089) N-((2,3-difluoro-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]-3,3,3-trifluoro-propanamide, (15.090) 1-methoxy-1-methyl-3-[[4-[5-(trifluoromethyl}-1,2,4-oxadiazol-3-yl]phenyl]methyl]urea, (15.091) 1,1-diethyl-3-[[4-[5-(trifluoromethyl}-1,2,4-oxadiazol-3-yl]phenyl]methyl]urea, (15.092) N-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]propanamide, (15.093) N-methoxy-N-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]-methyl]cyclopropanecarboxamide, (15.094) 1-methoxy-3-methyl-1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]urea, (15.095) N-methoxy-N-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl)cyclopropanecarboxamide, (15.096) N,2-dimethoxy-N-[[4-[5-(trifluoromethyl}-1,2,4-oxadiazol-3-yl]phenyl]-methyl]propanamide, (15.097) N-ethyl-2-methyl-N-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)phenyl]methyl]propanamide, (15.098) 1-methoxy-3-methyl-1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]urea, (15.099) 1,3-dimethoxy-1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]urea, (15.100) 3-ethyl-1-methoxy-1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]urea, (15.101) 1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]piperidin-2-one, (15.102) 4,4-dimethyl-2-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]-methyl]isooxazolidin-3-one, (15.103) 5,5-dimethyl-2-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]isoxazolidin-3-one, (15.104) 3,3-dimethyl-1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]piperidin-2-one, (15.105) 1-[[3-fluoro-4-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]azepan-2-one, (15.106) 4,4-dimethyl-2-[[4-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]isoxazolidin-3-one, (15.107) 5,5-dimethyl-2-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]-phenyl]methyl]isoxazolidin-3-one, (15.108) ethyl 1-{4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzyl}-1H-pyrazole-4-carboxylate, (15.109) N,N-dimethyl-1-{4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzyl}-1H-1,2,4-triazol-3-amine, (15.110) N-{2,3-difluoro-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzyl}butanamide, (15.111) N-(1-methylcyclopropyl)-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide, (15.112) N-(2,4-difluorophenyl)-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide, (15.113) 1-(5,6-dimethylpyridin-3-yl)-4,4-difluoro-3,3-dimethyl-3,4-dihydroisoquinoline, (15.114) 1-(6-(difluoromethyl)-5-methyl-pyridin-3-yl)-4,4-difluoro-3,3-dimethyl-3,4-dihydroisoquinoline, (15.115) 1-(5-(fluoromethyl)-6-methyl-pyridin-3-yl)-4,4-difluoro-3,3-dimethyl-3,4-dihydroisoquinoline, (15.116) 1-(6-(difluoromethyl)-5-methoxy-pyridin-3-yl)-4,4-difluoro-3,3-dimethyl-3,4-dihydroisoquinoline, (15.117) 4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl dimethylcarbamate, (15.118) N-{4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl}propanamide, (15.119) 3-[2-(1-{[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4-yl]-1,5-dihydro-2,4-benzodioxepin-6-yl methanesulfonate, (15.120) 9-fluoro-3-[2-(1-{[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4-yl]-1,5-dihydro-2,4-benzodioxepin-6-yl methanesulfonate, (15.121) 3-[2-(1-{[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4-yl]-1,5-dihydro-2,4-benzodioxepin-6-yl methanesulfonate, (15.122) 3-[2-(1-{[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4-yl]-9-fluoro-1,5-dihydro-2,4-benzodioxepin-6-yl methanesulfonate, (15.123) 1-(6,7-dimethylpyrazolo[1,5-a]pyridin-3-yl)-4,4-difluoro-3,3-dimethyl-3,4-dihydroisoquinoline, (15.124) 8-fluoro-N-(4,4,4-trifluoro-2-methyl-1-phenylbutan-2-yl)quinoline-3-carboxamide, (15.125) 8-fluoro-N-[(2S)-4,4,4-trifluoro-2-methyl-1-phenylbutan-2-yl]quinoline-3-carboxamide, (15.126) N-(2,4-dimethyl-1-phenylpentan-2-yl)-8-fluoroquinoline-3-carboxamide, (15.127) N-[(2S)-2,4-dimethyl-1-phenylpentan-2-yl]-8-fluoroquinoline-3-carboxamide, (15.128) D-tagatose. antibacterial agents selected from the group consisting of bacteria, such as (16.001) Bacillus subtilis, in particular strain QST713/AQ713 (available as SERENADE OPTI or SERENADE ASO from Bayer CropScience LP, US, having NRRL Accession No. B21661 and described in U.S. Pat. No. 6,060,051); (16.002) Bacillus amyloliquefaciens, in particular strain D747 (available as Double Nickel™ from Certis, US, having accession number FERM BP-8234 and disclosed in U.S. Pat. No. 7,094,592); (16.003) Bacillus pumilus, in particular strain BU F-33 (having NRRL Accession No. 50185); (16.004) Bacillus subtilis var. amyloliquefaciens strain FZB24 (available as Taegro® from Novozymes, US); (16.005) a Paenibacillus sp. strain having Accession No. NRRL B-50972 or Accession No. NRRL B-67129 and described in International Patent Publication No. WO 2016/154297; and fungi, such as (16.006) Aureobasidium pullulans, in particular blastospores of strain DSM14940; (16.007) Aureobasidium pullulans blastospores of strain DSM 14941; (16.008) Aureobasidium pullulans, in particular mixtures of blastospores of strains DSM14940 and DSM14941, biological fungicides selected from the group consisting of bacteria, for example (17.001) Bacillus subtilis, in particular strain QST713/AQ713 (available as SERENADE OPTI or SERENADE ASO from Bayer CropScience LP, US, having NRRL Accession No. B21661 and described in U.S. Pat. No. 6,060,051); (17.002) Bacillus pumilus, in particular strain QST2808 (available as SONATA® from Bayer CropScience LP, US, having Accession No. NRRL B-30087 and described in U.S. Pat. No. 6,245,551); (17.003) Bacillus pumilus, in particular strain GB34 (available as Yield Shield® from Bayer AG, DE); (17.004) Bacillus pumilus, in particular strain BU F-33 (having NRRL Accession No. 50185); (17.005) Bacillus amyloliquefaciens, in particular strain D747 (available as Double Nickel™ from Certis, US, having accession number FERM BP-8234 and disclosed in U.S. Pat. No. 7,094,592); (17.006) Bacillus subtilis Y1336 (available as BIOBAC® WP from Bion-Tech, Taiwan, registered as a biological fungicide in Taiwan under Registration Nos. 4764, 5454, 5096 and 5277); (17.007) Bacillus amyloliquefaciens strain MBI 600 (available as SUBTILEX from BASF SE); (17.008) Bacillus subtilis strain GB03 (available as Kodiak® from Bayer AG, DE); (17.009) Bacillus subtilis var. amyloliquefaciens strain FZB24 (available from Novozymes Biologicals Inc., Salem, Virginia or Syngenta Crop Protection, LLC, Greensboro, North Carolina as the fungicide TAEGRO® or TAEGRO® ECO (EPA Registration No. 70127-5); (17.010) Bacillus mycoides, isolate J (available as BmJ TGAI or WG from Certis USA); (17.011) Bacillus licheniformis, in particular strain SB3086 (available as EcoGuard™ Biofungicide and Green Releaf from Novozymes); (17.012) a Paenibacillus sp. strain having Accession No. NRRL B-50972 or Accession No. NRRL B-67129 and described in International Patent Publication No. WO 2016/154297, fatty acids or derivatives, for example (18.001) a composition comprising one or more fatty acids or derivatives thereof selected from unsaturated and saturated C₁₂-C₂₄ fatty acids, salts thereof, esters thereof or mixtures of any of the foregoing, wherein at least 95% of said fatty acids or derivatives thereof are in the range of C₁₄ to C₂₀.
 8. The active compound combination according to claim 1, wherein the further active compound (B) is selected from the group consisting of (1.002) difenoconazole, (1.018) prothioconazole, (1.020) spiroxamine, (1.021) tebuconazole, (1.055) mefentrifluconazole, (1.062) fluoxytioconazole, (1.067) N′-(2,5-dimethyl-4-{3-[(1,1,2,2-tetrafluoroethyl)sulfanyl]phenoxy}phenyl)-N-ethyl-N-methyl¬imido¬formamide, (2.002) bixafen, (2.005) fluopyram, (2.028) inpyrfluxam, (2.038) isoflucypram, (3.020) trifloxystrobin, (3.025) fenpicoxamid, (5.003) captan, (5.010) dithianon, (5.012) folpet, (5.013) mancozeb, (5.018) propineb, (6.002) isotianil, (7.005) pyrimethanil, (13.001) fludioxonil, (13.004) proquinazid, (13.005) quinoxyfen, (15.012) fosetyl-aluminium, (15.016) metrafenone, (15.043) fluoxa¬piprolin and (15.064) (N′-[2-chloro-4-(2-fluorophenoxy)-5-methylphenyl]-N-ethyl-N-methylimidoformamide), (17.001) Bacillus subtilis, in particular strain QST713/AQ713 (available as SERENADE OPTI or SERENADE ASO from Bayer CropScience LP, US, having NRRL Accession No. B21661 and described in U.S. Pat. No. 6,060,051), (17.012) a Paenibacillus sp. strain having Accession No. NRRL B-50972 or Accession No. NRRL B-67129 and described in International Patent Publication No. WO 2016/154297 and (18.001) a composition comprising one or more fatty acids or derivatives thereof selected from unsaturated and saturated C₁₂-C₂₄ fatty acids, salts thereof, esters thereof or mixtures of any of the foregoing, wherein at least 95% of said fatty acids or derivatives thereof are in the range of C₁₄ to C₂₀.
 9. A composition for controlling harmful microorganisms, in crop protection and in the protection of materials, comprising an active compound combination according to claim 1, in addition to at least one extender and/or surfactant.
 10. A method for controlling harmful microorganisms, in crop protection and in the protection of materials, comprising applying an active compound combination according to claim 1 to the harmful microorganisms and/or their habitat.
 11. The method of claim 10, wherein the harmful microorganisms are phytopathogenic harmful fungi.
 12. A method to treat a transgenic plant, comprising applying the active compound combination of claim 1 to the plant.
 13. A method to treat seed, comprising applying the active compound combination of claim 1 to the seed.
 14. A seed coated with the active compound combination of claim
 1. 15. The composition of claim 9, wherein the harmful microorganisms are phytopathogenic harmful fungi.
 16. The method of claim 13, wherein the seed is seed of a transgenic plant. 